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1.
In a deep, subalpine holo-oligomictic lake, the relative abundance of Archaea and Crenarchaeota, but not that of Bacteria, increases significantly with depth and varies seasonally. Cell-specific prokaryotic productivity is homogeneous along the water column. The concept of active Archaea observed in the deep ocean can therefore be extended to a deep oxic lake.The abundance, activity, and community composition of epilimnetic and hypolimnetic prokaryotes have been less thoroughly investigated in deep lakes than in oceans. Strong evidence that the depth gradient plays a role in modulating the balance between the domains of Bacteria and Archaea has been found in various marine systems (8, 12, 13, 20). It has been shown that the percentage of Bacteria in the deep marine hypolimnion decreases (up to 5,000 m) while, conversely, the percentage of Archaea increases. The percentage of Crenarchaeota is also higher in the mesopelagic zone than in surface waters (10).Although Archaea have been found in a variety of freshwater habitats (3), little has thus far been published on differentiating between Bacteria, Archaea, and Crenarchaeota in the hypolimnion of deep lakes. An exception is a study of the high-altitude ultraoligotrophic Crater Lake (21, 22), where group I marine Crenarchaeota were observed in deep-water populations (22). This study and another study of various lakes from three continents (9) are based on summer sampling, making it impossible to ascertain the effects of temporal variability on the vertical distribution of Archaea and Crenarchaeota, as has been done for marine systems and shallow lakes (for examples, see references 8 and 11).Our primary objective was to follow variations in the relative abundance of Bacteria, Archaea, and Crenarchaeota found in the hypolimnetic waters of a deep holo-oligomictic lake with a permanent oxic hypolimnion and compare them with those in the epilimnetic assemblages. We used the catalyzed reporter deposition fluorescence in situ hybridization (CARD-FISH) technique and compared the data thus obtained with prokaryotic productivity.  相似文献   

2.
The role of ammonia-oxidizing archaea (AOA) in nitrogen cycling in marine sediments remains poorly characterized. In this study, we enriched and characterized AOA from marine sediments. Group I.1a crenarchaea closely related to those identified in marine sediments and “Candidatus Nitrosopumilus maritimus” (99.1 and 94.9% 16S rRNA and amoA gene sequence identities to the latter, respectively) were substantially enriched by coculture with sulfur-oxidizing bacteria (SOB). The selective enrichment of AOA over ammonia-oxidizing bacteria (AOB) is likely due to the reduced oxygen levels caused by the rapid initial growth of SOB. After biweekly transfers for ca. 20 months, archaeal cells became the dominant prokaryotes (>80%), based on quantitative PCR and fluorescence in situ hybridization analysis. The increase of archaeal 16S rRNA gene copy numbers was coincident with the amount of ammonia oxidized, and expression of the archaeal amoA gene was observed during ammonia oxidation. Bacterial amoA genes were not detected in the enrichment culture. The affinities of these AOA to oxygen and ammonia were substantially higher than those of AOB. [13C]bicarbonate incorporation and the presence and activation of genes of the 3-hydroxypropionate/4-hydroxybutyrate cycle indicated autotrophy during ammonia oxidation. In the enrichment culture, ammonium was oxidized to nitrite by the AOA and subsequently to nitrate by Nitrospina-like bacteria. Our experiments suggest that AOA may be important nitrifiers in low-oxygen environments, such as oxygen-minimum zones and marine sediments.Archaea have long been known as extremophiles, since most cultivated archaeal strains were cultivated from extreme environments, such as acidic, hot, and high-salt environments. The view of archaea as extremophiles (i.e., acidophiles, thermophiles, and halophiles) has radically changed by the application of molecular technologies, including PCR in environmental microbiology. Using Archaea-specific PCR primers, novel archaeal 16S rRNA gene sequences were discovered in seawater (23, 27). Following these discoveries, an ever-increasing and unexpectedly high variety of archaeal 16S rRNA gene sequences has been reported from diverse “nonextreme” environments (67). This indicates that archaea are, like bacteria, ubiquitous in the biosphere rather than exclusively inhabiting specific extreme niches. Archaea are abundant in water columns of some oceanic provinces (33, 36) and deep-subsea floor sediments (11, 12, 48). Despite the increasing number of reports of the diversity and abundance of these nonextreme archaea by molecular ecological studies, their physiology and ecological roles have remained enigmatic.Oxidation of ammonia, a trait long thought to be exclusive to the domain Bacteria (13), was recently suggested to be a trait of archaea of the crenarchaeal groups I.1a and I.1b, based on a metagenome analysis (79) and supported by the discovery of archaeal amoA-like genes in environmental shotgun sequencing studies of Sargasso Sea water (80) and genomic analysis of “Candidatus Cenarchaeum symbiosum,” a symbiont of a marine sponge (30). Molecular ecological studies indicated that these ammonia-oxidizing archaea (AOA) are often predominant over ammonia-oxidizing bacteria (AOB) in ocean waters (9, 53, 87), soils (17, 47), and marine sediments (61). Critical evidence for autotrophic archaeal ammonia oxidation was obtained by the characterization of the first cultivated mesophilic crenarchaeon (group I.1a), “Candidatus Nitrosopumilus maritimus SCM1,” from an aquarium (38), and a related archaeon from North Sea water (87) and subsequently by enrichment of thermophilic AOA (22, 31). Whole-genome-based phylogenetic studies recently indicated that the nonthermophilic crenarchaea, including the AOA, likely form a phylum separate from the Crenarchaeota and Euryarchaeota phyla (15, 16, 72). This proposed new phylum was called Thaumarchaeota (15).Microorganisms in marine sediments contribute significantly to global biogeochemical cycles because of their abundance (85). Nitrification is essential to the nitrogen cycle in marine sediments and may be metabolically coupled with denitrification and anaerobic ammonium oxidation, resulting in the removal of nitrogen as molecular nitrogen and the generation of greenhouse gases, such as nitrous oxide (19, 75). Compared with studies on archaeal nitrification in the marine water column, only limited information on archaeal nitrification in marine sediments is available so far. Archaeal amoA genes have been retrieved from marine and coastal sediments (8, 26, 61), and the potentially important role of AOA in nitrification has been suggested based on the abundance of archaeal amoA genes relative to that of bacterial amoA genes in surface marine sediments from Donghae (South Korea) (61). Cultivation of AOA, although difficult (38), remains essential to estimating the metabolic potential of archaea in environments such as soils (47) and marine sediments (61). Here, we report the successful enrichment of AOA of crenarchaeal group I.1a from marine sediments by employing a coculture with sulfur-oxidizing bacteria (SOB) which was maintained for ca. 20 months with biweekly transfers. In this way, we were able to characterize AOA from marine sediments, providing a clue for the role of AOA in the nitrogen cycle of marine sediments.  相似文献   

3.
Molecular characterizations of environmental microbial populations based on recovery and analysis of DNA generally assume efficient or unbiased extraction of DNA from different sample matrices and microbial groups. Appropriate controls to verify this basic assumption are rarely included. Here three different DNA extractions, performed with two commercial kits (FastDNA and UltraClean) and a standard phenol-chloroform method, and two alternative filtration methods (Sterivex and 25-mm-diameter polycarbonate filters) were evaluated, using the addition of Nitrosopumilus maritimus cells to track the recovery of DNA from marine Archaea. After the comparison, a simplified phenol-chloroform extraction method was developed and shown to be significantly superior, in terms of both the recovery and the purity of DNA, to other protocols now generally applied to environmental studies. The simplified and optimized method was used to quantify ammonia-oxidizing Archaea at different depth intervals in a fjord (Hood Canal) by quantitative PCR. The numbers of Archaea increased with depth, often constituting as much as 20% of the total bacterial community.Efficient DNA extraction from environmental samples is fundamental to many culture-independent characterizations (10). Thus, there was an early and concerted effort to establish appropriate methods of DNA extraction from different types of environmental samples (14, 19, 25, 30, 34, 43, 47). DNA extraction efficiency is particularly important for quantitative PCR (qPCR), because poor DNA extraction efficiency results in the underestimation of gene copy numbers in the samples examined (6, 42).Most methodological developments addressed DNA extraction from soil and sediment samples, with fewer comparative studies of the efficiency of collection and extraction from water samples (4, 13, 40). In part, a methodological focus on soils reflected the simplicity of filtration to collect aquatic populations and the generally good recovery of DNA from the Gram-negative bacteria making up a significant fraction of aquatic communities. However, small Archaea are now known to constitute a substantial fraction of the prokaryotic populations in marine and terrestrial systems (2, 7, 9, 20, 26, 31, 33, 45). Since the archaeal cell wall and membrane structures are distinct from those of bacteria, there is no assurance that commonly used extraction methods are adequate. With increasing reliance on commercially available bead-beating-type DNA extraction kits, these methods are now often used for different water samples (1, 5-7, 14, 19, 36). Although most protocols incorporate mechanical disruption to ensure more-uniform extraction than is possible by using methods that rely entirely on enzymatic digestion and/or chemical disruption (4, 13, 40), the suitability of these protocols for the concerted analysis of archaeal and bacterial populations has not been fully evaluated.In the studies reported here, the recently isolated marine archaeon Nitrosopumilus maritimus strain SCM1 (22) was therefore used as a reference standard for evaluation of the commonly employed DNA extraction methods by using qPCR. This archaeon was then used as a reference for the development of a simple, rapid, and efficient method of extracting DNA from both archaeal and bacterial cells. The modified protocol was subsequently employed to characterize the vertical distribution of ammonia-oxidizing Archaea in a fjord (Hood Canal) in Puget Sound (Washington State), revealing a high fractional representation of Archaea relative to Bacteria not observed previously in coastal waters.  相似文献   

4.
The bacterioneuston is the community of Bacteria present in surface microlayers, the thin surface film that forms the interface between aquatic environments and the atmosphere. In this study we compared bacterial cell abundances and bacterial community structures of the bacterioneuston and the bacterioplankton (from the subsurface water column) during a phytoplankton bloom mesocosm experiment. Bacterial cell abundance, determined by flow cytometry, followed a typical bacterioplankton response to a phytoplankton bloom, with Synechococcus and high-nucleic acid content (HNA) bacterial cell numbers initially falling, probably due to selective protist grazing. Subsequently HNA and low-nucleic acid content bacterial cells increased in abundance, but Synechococcus cells did not. There was no significant difference between bacterioneuston and bacterioplankton cell abundances during the experiment. Conversely, distinct and consistent differences between the bacterioneuston and the bacterioplankton community structures were observed. This was monitored simultaneously by Bacteria 16S rRNA gene terminal restriction fragment length polymorphism and denaturing gradient gel electrophoresis. The conserved patterns of community structure observed in all of the mesocosms indicate that the bacterioneuston is distinctive and nonrandom.Determining and understanding both spatial and temporal patterns in bacterioplankton community structure are a core aim of marine microbial ecology (15). Distributions of bacterioplankton over space and time can be correlated to environmental parameters, and subsequent links can therefore be made to ecosystem function. A broad range of spatial studies made on macro- (34), meso- (20), and microscales (27) have shown clear patterns in distribution of the bacterioplankton.The sea surface microlayer is part of the air-sea interface and is generally considered to be the top 1 mm or less of the ocean (26). Surface microlayers have a fundamental role in regulating transport processes between the ocean and the atmosphere (26) and are often referred to as the neuston (28, 31). For more than 25 years it has been hypothesized that the sea surface microlayer is a hydrated gelatinous layer (40) that contains surface-active organic compounds such as carbohydrates, proteins, lipids, and humic substances in relatively high concentrations (17, 45, 48). Recently, gel-like transparent expolymer particles (TEP) have been shown to be enriched in the surface microlayer, supporting the concept of a gelatinous interfacial layer (46).Bacteria present in surface microlayers or the neuston are regarded as the bacterioneuston. There are relatively few studies which have directly compared the community structure of the bacterioneuston with that of the cognate subsurface (bacterioplankton) in the marine environment. Analysis of Bacteria 16S rRNA gene clone libraries constructed using DNA isolated from surface microlayer and subsurface water (<1 m) samples from the North Sea revealed that the bacterioneuston was dominated by two operational taxonomic units which accounted for 81% of clones analyzed (13). Community structure profiling using denaturing gradient gel electrophoresis (DGGE) of the bacterioneuston at three sites around Oahu Island in the Pacific Ocean showed that the bacterioneuston forms consistent and distinct community structures. Conversely, the archaeal community structure of the same samples using Archaea 16S rRNA gene DGGE analysis did not show the same surface microlayer-specific response, indicating that bacteria and archaea respond to their environment in fundamentally different ways in the neuston (7).Other studies have, however, reported no consistent differences between the bacterioneuston and the bacterioplankton. Samples collected from two separate sites in the Mediterranean Sea were analyzed using single-strand conformation polymorphism of Bacteria 16S rRNA genes (1). The authors did not report any significant differences between the surface microlayer and subsurface samples using this community profiling method.Nonmarine studies of the bacterioneuston and Archaea communities in estuarine (10) and freshwater (5, 19) environments have also shown distinct microbial community structures present in the surface microlayer compared to those in subsurface water ≤1 m below.Recurring phytoplankton blooms are a key feature of coastal waters and strongly influence bacterioplankton community structure and succession (4, 14, 38). Phytoplankton blooms stimulate the bacterioplankton by the release of dissolved organic matter (22) or affect bacterioplankton negatively by direct competition for resources (6). Bacterioplankton community structure may also be influenced by grazing flagellates or viral lysis (47).Mesocosm experiments have been used to study plankton ecology for many decades (33). Mesocosms facilitate study of the effects of key environmental parameters, such as temperature, on plankton communities and allow the succession of natural plankton communities that resemble those found in the marine environment (11). The enclosed water mass means that experiments can be designed which manipulate physicochemical parameters to observe biological effects. Furthermore, with replicated mesocosms, the data collected can be analyzed with statistics rigorously. In this study we monitored the dynamics of the bacterioneuston and the bacterioplankton in mesocosms of fjord surface water during an artificially induced phytoplankton bloom and compared bacterial abundances and bacterial community structures in the surface microlayer and subsurface water.  相似文献   

5.
A disease-like syndrome is currently affecting a large percentage of the Ianthella basta populations from the Great Barrier Reef and central Torres Strait. Symptoms of the syndrome include discolored, necrotic spots leading to tissue degradation, exposure of the skeletal fibers, and disruption of the choanocyte chambers. To ascertain the role of microbes in the disease process, a comprehensive comparison of bacteria, viruses, fungi, and other eukaryotes was performed in healthy and diseased sponges using multiple techniques. A low diversity of microbes was observed in both healthy and diseased sponge communities, with all sponges dominated by an Alphaproteobacteria, a Gammaproteobacteria, and a group I crenarchaeota. Bacterial cultivation, community analysis by denaturing gradient gel electrophoresis (Bacteria and Eukarya), sequencing of 16S rRNA clone libraries (Bacteria and Archaea), and direct visual assessment by electron microscopy failed to reveal any putative pathogens. In addition, infection assays could not establish the syndrome in healthy sponges even after direct physical contact with affected tissue. These results suggest that microbes are not responsible for the formation of brown spot lesions and necrosis in I. basta.Sponges harbor a highly diverse range of microorganisms, including representatives from 28 bacterial phyla and both major lineages of the Archaea (reference 34 and references cited therein; 40). Microorganisms can comprise up to 40% of sponge biomass, although sponges with more developed aquiferous systems and looser mesohyl often have lower microbial abundances (35). Some sponge-microbe associations may be considered symbiotic (34), while others are nonspecific and may include potentially pathogenic microorganisms (7, 41).Diseases of marine organisms have been attributed to bacteria, fungi, viruses, protozoans, and a variety of metazoan parasites (18). In sponges, bacteria and fungi are the most commonly reported pathogens, but the exact etiological agents are rarely identified, and little is known about the disease processes (38). In the past decade there has been an increase in reports of sponge disease around the globe, including the Caribbean, Panama, Papua New Guinea, and Slovenia (7, 14, 27, 29, 41, 44). Disease-like symptoms in sponges may also arise from environmental stressors (4, 17), physical damage (46), predation (20), or competitive interactions (22).Since 2006, two studies have reported a disease-like syndrome in the sponge Ianthella basta, which is commonly distributed in Papua New Guinea (7) and along the Great Barrier Reef (24). A large percentage of I. basta sponges from the Torres Strait and the Palm Islands in the Great Barrier Reef were found to exhibit signs of disease, which included discolored, necrotic spots and exposed skeletal fibers (24). In sponges affected by this syndrome there was a high level of cellular degradation and debris within the remnants of the choanocyte chambers. In Papua New Guinea, I. basta exhibited high mortality between 1996 and 2000, with the affected sponges exhibiting mottled brown lesions, rotted tissue, and large holes (7). The etiological agent of disease in I. basta was not unequivocally ascertained in either study.Previous research using 454 tag pyrosequencing has assessed the microbial community in I. basta and reported high diversity, with 1,099 operational taxonomic units (OTU) at 95% sequence similarity (40). However, most of this diversity was composed of rare organisms represented by only one or a few sequences. The community was dominated by the Alpha- and Gammaproteobacteria with a single Gammaproteobacteria OTU actually comprising 49% of all sequence tags (40). The rare microbial biosphere in I. basta included Acidobacteria, Actinobacteria, Bacteroidetes, Chlamydiae, Chloroflexi, Cyanobacteria, Deinococcus-Thermus, Firmicutes, Gemmatimonadetes, Lentisphaerae, Nitrospira, Planctomyces, Poribacteria, Spirochaetes, TM7, Verrucomicrobia, and the beta, delta, and epsilon classes of the Proteobacteria (40).With bacteria commonly implicated in sponge disease processes and shifts in microbial communities being used to detect putative pathogens in corals and sponges (3, 7, 33, 41), we sought to ascertain the role of microorganisms in the disease-like syndrome affecting I. basta and to determine how disease affects the symbiotic microbial population.  相似文献   

6.
7.
Diversity and abundance of ammonia-oxidizing Betaproteobacteria (β-AOB) and archaea (AOA) were investigated in a New England salt marsh at sites dominated by short or tall Spartina alterniflora (SAS and SAT sites, respectively) or Spartina patens (SP site). AOA amoA gene richness was higher than β-AOB amoA richness at SAT and SP, but AOA and β-AOB richness were similar at SAS. β-AOB amoA clone libraries were composed exclusively of Nitrosospira-like amoA genes. AOA amoA genes at SAT and SP were equally distributed between the water column/sediment and soil/sediment clades, while AOA amoA sequences at SAS were primarily affiliated with the water column/sediment clade. At all three site types, AOA were always more abundant than β-AOB based on quantitative PCR of amoA genes. At some sites, we detected 109 AOA amoA gene copies g of sediment−1. Ratios of AOA to β-AOB varied over 2 orders of magnitude among sites and sampling dates. Nevertheless, abundances of AOA and β-AOB amoA genes were highly correlated. Abundance of 16S rRNA genes affiliated with Nitrosopumilus maritimus, Crenarchaeota group I.1b, and pSL12 were positively correlated with AOA amoA abundance, but ratios of amoA to 16S rRNA genes varied among sites. We also observed a significant effect of pH on AOA abundance and a significant salinity effect on both AOA and β-ΑΟΒ abundance. Our results expand the distribution of AOA to salt marshes, and the high numbers of AOA at some sites suggest that salt marsh sediments serve as an important habitat for AOA.Nitrification, the sequential oxidation of ammonia to nitrite and nitrate, is a critical step in the nitrogen cycle and is mediated by a suite of phylogenetically and physiologically distinct microorganisms. The recent discovery of ammonia oxidation among Archaea (17, 38) has led to a dramatic shift in the current model of nitrification and to new questions of niche differentiation between putative ammonia-oxidizing Archaea (AOA) and the more-well-studied ammonia-oxidizing Betaproteobacteria (β-AOB). Based on surveys of 16S rRNA genes and archaeal amoA genes, it is evident that AOA occupy a wide range of niches (10), suggesting a physiologically diverse group of Archaea. Additionally, in studies where AOA and β-AOB were both targeted, AOA were typically more abundant than their bacterial counterparts (19, 21, 42). However, there are reports of β-AOB outnumbering AOA in estuarine systems (6, 33), suggesting a possible shift in competitive dominance under certain conditions.Patterns of β-AOB diversity in estuaries have been well characterized and appear to be regulated by similar mechanisms within geographically disparate systems (4, 11, 32). However, AOA distribution and their role in nitrification relative to β-AOB remain to be determined. A few studies have begun to address this question in different estuaries, but no unifying patterns or mechanisms have emerged. Although β-AOB have been well studied along estuarine salinity gradients (1, 3, 4, 7, 11, 13, 22, 33, 39) and recent studies have begun to address AOA in estuaries (1, 6, 22, 32, 33), few have investigated β-AOB in salt marshes (9), and none has included AOA.In this study, we investigated the distribution and abundance of AOA and β-AOB based on the distribution and abundance of amoA genes in salt marsh sediments dominated by different types of vegetation. Although we equate the presence of archaeal amoA genes with the genetic potential to oxidize ammonia, we acknowledge the possibility that all Archaea that have amoA genes may not all represent functional ammonia oxidizers. Vegetation patterns of New England salt marshes are strongly correlated with marsh elevation and are controlled by a combination of interspecific competition and tolerance to physico-chemical stress (28). The dominant grasses of New England salt marshes are Spartina alterniflora and Spartina patens, which typically grow as pure stands. S. alterniflora is found in two phenotypically distinct but genetically identical forms, a tall and a short growth form (34). The tall S. alterniflora grows to heights of 1 to 2 m and is typically found at the edges of the marsh and along creek banks (SAT sites), while the short-form S. alterniflora may reach heights of only 30 cm and is found in sites (SAS sites) slightly higher on the marsh where soil drainage is limited and conditions are more reduced compared to SAT sites (14). Conversely, S. patens, due to its lower tolerance of salt and more reduced conditions, is found in sites (SP sites) highest on the marsh, in areas that receive less flooding (5). Because the marsh is subjected to daily tidal fluctuations, most sites experience periods of anoxia, the degree of which depends on the marsh elevation. We hypothesized that ammonia-oxidizing communities in areas dominated by different marsh grasses would reflect the different edaphic conditions associated with each type of grass, due to differences in vertical zonation in the marsh.  相似文献   

8.
Crenarchaeol, a membrane-spanning glycerol dialkyl glycerol tetraether (GDGT) containing a cyclohexane moiety in addition to four cyclopentane moieties, was originally hypothesized to be synthesized exclusively by the mesophilic Crenarchaeota. Recent studies reporting the occurrence of crenarchaeol in hot springs and as a membrane constituent of the recently isolated thermophilic crenarchaeote “Candidatus Nitrosocaldus yellowstonii,” however, have raised questions regarding its taxonomic distribution and function. To determine whether crenarchaeol in hot springs is indeed synthesized by members of the Archaea in situ or is of allochthonous origin, we quantified crenarchaeol present in the form of both intact polar lipids (IPLs) and core lipids in sediments of two California hot springs and in nearby soils. IPL-derived crenarchaeol (IPL-crenarchaeol) was found in both hot springs and soils, suggesting in situ production of this GDGT over a wide temperature range (12°C to 89°C). Quantification of archaeal amoA gene abundance by quantitative PCR showed a good correspondence with IPL-crenarchaeol, suggesting that it was indeed derived from living cells and that crenarchaeol-synthesizing members of the Archaea in our samples may also be ammonia oxidizers.Numerous groups of the Archaea synthesize isoprenoid glycerol dialkyl glycerol tetraethers (GDGTs) as a major component of their core membrane lipids, which can contain up to eight cyclopentane moieties (e.g., see reference 7) (Fig. (Fig.1).1). An increase in the number of cyclopentane moieties results in denser packing of membrane lipids, allowing for the maintenance of both cellular membrane integrity at high temperatures and stable proton gradients under low-pH conditions (8). This biophysical characteristic is hypothesized to be among those traits essential for the survival and persistence of the Archaea in the “extreme” environments in which they are commonly found (42). GDGTs are synthesized by a large number of cultivated members of the Archaea (see overviews in references 20 and 34), and in nature, they are abundant in hot springs (24, 25, 34, 46), for example, where members of the Archaea are known to thrive at high temperatures and over a wide pH range (3, 21).Open in a separate windowFIG. 1.Structures of GDGTs referred to in the text. “IS,” C46 internal standard.Crenarchaeol is unique among the GDGTs in that it contains a cyclohexane moiety in addition to four cyclopentane moieties (Fig. (Fig.1).1). It was first reported in large abundances from Holocene and ancient sediments collected from various marine settings as supporting evidence for the widespread distribution of low-temperature relatives of the hyperthermophilic Archaea (31). It was later proposed that crenarchaeol was synthesized exclusively by marine group I Crenarchaeota (36), a hypothesis further supported by core lipid analysis of the mesophilic marine group I.1a crenarchaeotes “Cenarchaeum symbiosum” (38) and “Candidatus Nitrosopumilus maritimus” SCM1 (30), which showed that both of these organisms synthesize crenarchaeol at moderate temperatures. In addition to this, the apparent absence of crenarchaeol in cultures of (hyper)thermophilic members of the Archaea (see overviews in references 20 and 34) and molecular modeling (8, 37) led to the hypothesis that crenarchaeol decreases lipid density, effectively allowing archaeal membranes composed of membrane-spanning GDGTs to function at mesophilic temperatures (37). Hence, crenarchaeol synthesis was thought to be instrumental in the evolution and radiation of mesophilic Crenarchaeota from thermophilic habitats (17).Recent studies, however, have reported the occurrence of crenarchaeol in hot springs with temperatures of up to 86.5°C (24, 25, 34, 46). That work has been debated to some extent, as there exists the potential for the allochtonous input of fossilized lipid material from weathering of nearby soils where mesophilic Crenarchaeota may thrive: Schouten et al. (34) previously found large relative amounts of specific soil bacterium biomarkers in tandem with crenarchaeol in Yellowstone hot springs. In contrast, Reigstad et al. (28) reported the occurrence of crenarchaeol in the absence of soil-specific biomarkers in Icelandic hot springs. Furthermore, the recently isolated thermophilic crenarchaeote “Candidatus Nitrosocaldus yellowstonii” was shown to synthesize crenarchaeol at a growth temperature of 72°C (6).Core lipids (CLs) that occur in biological membranes generally contain polar head groups such as sugars and phosphates, which are rapidly cleaved upon cell senescence (10, 44). The loss of head groups from intact polar lipids (IPLs) leaves relatively recalcitrant CLs to accumulate in the environment over time as fossil biomarkers. Therefore, depending on the extraction and/or analytical protocols, CLs present in environmental lipid extracts may be derived from both living cells and fossil biomass, including a mixture of both CL-derived GDGTs (CL-GDGTs) and IPL-derived GDGTs (IPL-GDGTs). Most studies of the presence of crenarchaeol in hot springs reported to date have analyzed directly extracted CL-crenarchaeol or CL-crenarchaeol released by the acid hydrolysis of Bligh-Dyer IPL lipid extracts, i.e., without prior separation of CL-GDGTs from IPL-GDGTs (24, 25, 28, 34, 46). In these cases, the reported GDGT distributions represent an integrated signal of both “living” and fossilized material, rendering it impossible to distinguish what proportion (if any) of the observed crenarchaeol was derived from local living archaeal communities. Thus, the in situ production of crenarchaeol in hot springs and its importance relative to that of the in situ production of other archaeal GDGTs remain uncertain.Here we have used a recently described chromatographic method (22, 26) to separately quantify the potential contributions of both in situ-produced and fossilized crenarchaeol (as well as other archaeal GDGTs) in two Californian hot springs and their surrounding soils. In addition, we have quantified the amounts of archaeal amoA and archaeal 16S rRNA gene copies from one site to make quantitative comparisons between gene abundance and IPL-GDGT concentrations.  相似文献   

9.
10.
Dissimilatory NO3 reduction in sediments is often measured in bulk incubations that destroy in situ gradients of controlling factors such as sulfide and oxygen. Additionally, the use of unnaturally high NO3 concentrations yields potential rather than actual activities of dissimilatory NO3 reduction. We developed a technique to determine the vertical distribution of the net rates of dissimilatory nitrate reduction to ammonium (DNRA) with minimal physical disturbance in intact sediment cores at millimeter-level resolution. This allows DNRA activity to be directly linked to the microenvironmental conditions in the layer of NO3 consumption. The water column of the sediment core is amended with 15NO3 at the in situ 14NO3 concentration. A gel probe is deployed in the sediment and is retrieved after complete diffusive equilibration between the gel and the sediment pore water. The gel is then sliced and the NH4+ dissolved in the gel slices is chemically converted by hypobromite to N2 in reaction vials. The isotopic composition of N2 is determined by mass spectrometry. We used the combined gel probe and isotopic labeling technique with freshwater and marine sediment cores and with sterile quartz sand with artificial gradients of 15NH4+. The results were compared to the NH4+ microsensor profiles measured in freshwater sediment and quartz sand and to the N2O microsensor profiles measured in acetylene-amended sediments to trace denitrification.Nitrate accounts for the eutrophication of many human-affected aquatic ecosystems (19, 21). Sediment bacteria may mitigate NO3 pollution by denitrification and anaerobic ammonium oxidation (anammox), which produce N2 (13, 18). However, inorganic nitrogen is retained in aquatic ecosystems when sediment bacteria reduce NO3 to NH4+ by dissimilatory nitrate reduction to ammonium (DNRA) (5, 12, 16, 39). Hence, DNRA contributes to rather than counteracts eutrophication (23). DNRA may be the dominant pathway of dissimilatory NO3 reduction in sediments that are rich in electron donors, such as labile organic carbon and sulfide (4, 8, 17, 38, 55). High rates of DNRA are thus found in sediments affected by coastal aquaculture (8, 36) and settling algal blooms (16).DNRA, denitrification, and the chemical factors that control the partitioning between them (e.g., sulfide) should ideally be investigated in undisturbed sediments. The redox stratification of sediments involves vertical concentration gradients of pore water solutes. These gradients are often very steep, and their measurement requires high-resolution techniques, such as microsensors (26, 42) and gel probes (9, 54). If, for instance, the influence of sulfide on DNRA and denitrification is to be investigated, one wants to know exactly the sulfide concentration in the layers of DNRA and denitrification activity, as well as the flux of sulfide into these layers. This information can easily be obtained using H2S and pH microsensors (22, 43). It is less trivial to determine the vertical distribution of DNRA and denitrification activity in undisturbed sediments. Denitrification activity can be traced using a combination of the acetylene inhibition technique (51) and N2O microsensors (1). Acetylene inhibits the last step of denitrification, and therefore, N2O accumulates in the layer of denitrification activity (44). This method underestimates the denitrification activity in sediments with high rates of coupled nitrification-denitrification because acetylene also inhibits nitrification (50).The vertical distribution of DNRA activity in undisturbed sediment has, to the best of our knowledge, never been determined; thus, the microenvironmental conditions in the layer of DNRA activity remain unknown. Until now, the influence of chemical factors on DNRA and denitrification in sediments has been assessed by slurry incubations (4, 12, 30), by flux measurements with sealed sediment cores (7, 47) or flowthrough sediment cores (16, 27, 37), and in one case, in reconstituted sediment cores sliced at centimeter-level resolution (39). Here, we present a new method, the combined gel probe and isotope labeling technique, to determine the vertical distribution of the net rates of DNRA in sediments. The sediments remain largely undisturbed and the NO3 amendments are within the range of in situ concentrations. The DNRA measurements can be related to the microprofiles of potential influencing factors measured in close vicinity of the gel probe. This allows DNRA activity to be directly linked with the microenvironmental conditions in the sediment.  相似文献   

11.
Proteorhodopsins (PRs) are widespread bacterial integral membrane proteins that function as light-driven proton pumps. Antarctic sea ice supports a complex community of autotrophic algae, heterotrophic bacteria, viruses, and protists that are an important food source for higher trophic levels in ice-covered regions of the Southern Ocean. Here, we present the first report of PR-bearing bacteria, both dormant and active, in Antarctic sea ice from a series of sites in the Ross Sea using gene-specific primers. Positive PR sequences were generated from genomic DNA at all depths in sea ice, and these sequences aligned with the classes Alphaproteobacteria, Gammaproteobacteria, and Flavobacteria. The sequences showed some similarity to previously reported PR sequences, although most of the sequences were generally distinct. Positive PR sequences were also observed from cDNA reverse transcribed from RNA isolated from sea ice samples. This finding indicates that these sequences were generated from metabolically active cells and suggests that the PR gene is functional within sea ice. Both blue-absorbing and green-absorbing forms of PRs were detected, and only a limited number of blue-absorbing forms were found and were in the midsection of the sea ice profile in this study. Questions still remain regarding the protein''s ecological functions, and ultimately, field experiments will be needed to establish the ecological and functional role of PRs in the sea ice ecosystem.Proteorhodopsins (PRs) are retinal binding bacterial integral membrane proteins that function as light-driven proton pumps (9, 10) and belong to the microbial rhodopsin superfamily of proteins (54). Since the first reported PR sequence from members of SAR86 clade marine (class Gammaproteobacteria) in 2000 (9), many other PR-bearing bacteria have been identified in a range of marine habitats (5, 18, 20, 24, 25, 46, 62). In the recent Global Ocean Sampling (GOS) expedition, almost 4,000 PR sequences from 41 distinct surface marine environments were acquired, demonstrating that these PR genes are extremely abundant in the genomes of ocean bacterioplankton (46). In fact, PR-containing bacteria account for 13% of the community in the Mediterranean Sea and Red Sea and 70% of the community in the Sargasso Sea (18, 46, 49, 60). These light-harvesting bacteria are present in three major marine classes of bacteria: the Alphaproteobacteria, Gammaproteobacteria, and Flavobacteria. In addition, two distinct PR genes encode pigments with “blue-absorbing” and “green-absorbing” properties, which is achieved by a substitution at a single amino acid position, which thereby functions as a spectral tuning switch (10, 37, 48).Sea ice represents a complex physicochemical environment in polar regions and covers up to 13% of the Earth''s surface (59). Although extreme gradients of temperature, salinity, nutrient availability, and light stratify the ice matrix from the surface to the ice-water interface (41), the sea ice habitat nevertheless supports a diverse microbial community of phytoplankton, Bacteria, Archaea, viruses, and protists that grow in liquid brine channels within the ice (14, 35, 56). This sea ice microbial community (SIMCO) is highly metabolically active despite being unable to avoid the extreme environmental conditions that they experience (39). In fact, very-high-standing stocks of the SIMCO exist in many regions of the Southern Ocean. For example, the concentration of chlorophyll a, a proxy for microalgal biomass, typically reaches 200 mg m2 in the Ross Sea, while the concentration of chlorophyll a in the water column below is approximately 2 orders of magnitude less (47), and the percentage of metabolically active bacteria (32% [39]) is significantly higher than the 10% observed for temperate marine systems (36). The SIMCO is thus a major source of biomass in ice-covered regions of the Southern Ocean (59), providing a critical food source for grazing zooplankton (and, consequently, also for higher trophic levels) for much of the year (3, 59). This biomass is of particular importance during the darkness of the polar winter, where the bottom-ice community is the only available food source for juvenile krill. These grazers absolutely rely on the sea ice microbial community to survive, as the water lacks other food sources (6, 28).In the past decade, reports of the widespread occurrence of bacteriochlorophyll and PR pigments in planktonic marine bacteria have challenged the assumption that chlorophyll a is the only principal light-capturing pigment in ocean surface waters. These alternative pigments may in fact play a critical role in light energy harvesting for microbial metabolism in various aquatic ecosystems (5, 10, 25, 40, 49). It has been proposed that energy, rather than nutrient conservation, is important for the regulation of productivity (7). PR-containing phototrophic eubacteria could play a significant role in the energy budget of cells in the photic zone in marine environments (15). PR sequences have been detected in the Southern Ocean (9), but to our knowledge, there have been no reports of PR-bearing bacteria within the sea ice matrix.The majority of the microbial rhodopsin genes found in oceanic samples have been detected by environmental sequencing (30, 46, 48, 60). We have used degenerate PR gene primers (5) in this study to positively identify PR-bearing operational taxonomic units (OTUs) from sea ice. Also, specific bacterial mRNA can now be detected from extracted nucleic acids and used to examine gene expression and, thus, infer metabolic activity (8). With this in mind, we have generated cDNA from RNA extracted from sea ice samples. From these observations, we deduce that PR-bearing bacteria are present in sea ice and may be actively contributing to the ecosystem within this extreme microenvironment.  相似文献   

12.
In the present study, we investigated a group of uncultivated magnetotactic cocci, which was magnetically isolated from a freshwater pond in Beijing, China. Light and transmission electron microscopy showed that these cocci ranged from 1.5 to 2.5 μm and contained two to four chains of magnetite magnetosomes, which sometimes were partially disorganized. Overall, the size of the disorganized magnetosomes was significantly smaller than that arranged in chains. All characterized magnetosome crystals were elongated (shape factor = 0.64) and fall into the single-domain size range (30 to 115 nm). Comparative 16S rRNA gene sequence analysis and fluorescence in situ hybridization showed that the enriched bacteria were a virtually homogeneous population and represented a novel lineage in the Alphaproteobacteria. The closest cultivated relative was magnetotactic coccoid strain MC-1 (88% sequence identity). First-order reversal curve diagrams revealed that these cocci had relatively strong magnetic interactions compared to the single-chain magnetotactic bacteria. Low-temperature magnetic measurements showed that the Verwey transition of them was ∼108 K, confirming magnetite magnetosomes, and the delta ratio δFCZFC was >2. Based on the structure, phylogenetic position and magnetic properties, the enriched magnetotactic cocci of Alphaproteobacteria are provisionally named as “Candidatus Magnetococcus yuandaducum.”Magnetotactic bacteria (MTB) can mineralize intracellular nanosized iron oxides or sulfides called magnetosomes, which in most MTB are normally single-domain (SD) magnetite with a narrow range of grain sizes from 30 to 120 nm (3). The chain configuration of magnetosomes renders MTB able to navigate the oxic-anoxic interface in chemically stratified environments by swimming along the Earth''s magnetic field (13). Diverse MTB, including coccoid, spirillar, rod-shaped bacteria and multicellular magnetotactic prokaryotes with one, two, or more chains of magnetosomes, thrive in a broad range of aquatic environments, which sometimes even are dominant strains of the microbial biomass in sediment (10, 47). Based on their phylogeny, all currently known MTB can be divided into two taxonomic groups: Proteobacteria and Nitrospira phyla (2).When MTB die, the magnetosomes can be preserved in sediment as fossil magnetosomes (or magnetofossils) (6). Fossil magnetosomes have been found in lacustrine and deep-sea sediments (6, 35, 43, 51), which are stable carriers of natural remanence and may play substantial contributions to the bulk magnetization of sediments due to their SD sizes (6, 19, 26, 32, 33). Moreover, since most known MTB are microaerophilic or anaerobic and are concentrated in the oxic-anoxic transition zone, the presence and characteristics of MTB species in vertically stratified sediments can be used as a potential paleoenvironmental proxy (19, 44, 45). However, how to identify bacterial magnetite or greigite (Fe3S4) in sediments is still challenging. Recently, characterizing the magnetic properties of MTB has attracted increasing interests because magnetic techniques are fast and effective in distinguishing bacterial crystals from abiogenic magnetic minerals in sediments (11, 26, 27, 33, 38).In spite of their wide distribution and abundance in aquatic environments, most MTB are intractable, and so far only a few of them, e.g., Magnetospirillum gryphiswaldense strain MSR-1 (41), M. magnetotacticum strain AMB-1 (17), M. magnetotacticum strain MS-1 (4), and magnetotactic coccoid strain MC-1 (24), can be grown in pure culture. Until recently, most insights into the molecular characterizations and magnetic properties of MTB have been based on pure cultures, which have a single magnetosome chain per cell (10, 11, 19, 20, 25, 27, 28, 37, 38, 42, 52). However, knowledge of uncultivated MTB, especially strains with multiple chains of magnetosomes that are commonly encountered in natural environments, remains limited. In the present study, we investigated a population of uncultivated magnetotactic cocci with multiple magnetosome chains, which were abundant in the pond in Yuan Dynasty Capital City Wall Relics Park (Yuandadu Park) in Beijing, China, in order to characterize their morphological features, phylogenetic positions, and magnetic properties and finally to classify them in a provisional Candidatus taxon.  相似文献   

13.
Sulfate-reducing bacteria (SRB) play a major role in the coupled biogeochemical cycling of sulfur and chalcophilic metal(loid)s. By implication, they can exert a strong influence on the speciation and mobility of multiple metal(loid) contaminants. In this study, we combined DsrAB gene sequencing and sulfur isotopic profiling to identify the phylogeny and distribution of SRB and to assess their metabolic activity in salt marsh sediments exposed to acid mine drainage (AMD) for over 100 years. Recovered dsrAB sequences from three sites sampled along an AMD flow path indicated the dominance of a single Desulfovibrio species. Other major sequence clades were related most closely to Desulfosarcina, Desulfococcus, Desulfobulbus, and Desulfosporosinus species. The presence of metal sulfides with low δ34S values relative to δ34S values of pore water sulfate showed that sediment SRB populations were actively reducing sulfate under ambient conditions (pH of ∼2), although possibly within less acidic microenvironments. Interestingly, δ34S values for pore water sulfate were lower than those for sulfate delivered during tidal inundation of marsh sediments. 16S rRNA gene sequence data from sediments and sulfur isotope data confirmed that sulfur-oxidizing bacteria drove the reoxidation of biogenic sulfide coupled to oxygen or nitrate reduction over a timescale of hours. Collectively, these findings imply a highly dynamic microbially mediated cycling of sulfate and sulfide, and thus the speciation and mobility of chalcophilic contaminant metal(loid)s, in AMD-impacted marsh sediments.Salt marshes exhibit high primary production rates (1, 101) and form biogeochemical “transition zones” for nutrient production, transport, and cycling between terrestrial and coastal marine environments (41, 66, 100). These zones also serve to reduce the flux of potentially toxic metals in contaminated groundwater to estuaries (12, 99, 106). Both functions depend strongly on microbial activity, especially that of sulfate-reducing bacteria (SRB) (42, 62, 67). SRB recycle much of the sedimentary organic carbon pool in marsh sediments (42-44) and indirectly inhibit production of the greenhouse gas methane (37, 71). They can restrict the mobility of dissolved contaminant metals by inducing precipitation of poorly soluble metal sulfides, and studies have examined their use in constructed wetlands to bioremediate acid mine drainage (AMD) and other metalliferous waste streams (11, 35, 40, 46, 50, 76, 90, 94, 104). However, the high acidity and metal concentrations inherent to AMD can inhibit SRB growth (15, 88, 98), and preferential growth of iron- and sulfur-oxidizing bacteria over SRB has been observed in some treatment wetlands (39).For natural salt marshes, 16S ribosomal nucleic acid- and phospholipid fatty acid (PLFA)-based analyses have shown that SRB commonly comprise a significant fraction of the microbial community (13, 24, 31, 34, 51, 58). Studies of salt marsh dissimilatory sulfite reductase genes (dsrAB), a highly conserved functional phylogenetic marker of prokaryotic sulfate reducers (49, 57, 102, 103, 107), have revealed both novel and deeply branching clades (3). Studies of mining-impacted sites at pH 2.0 to 7.8 (5, 7, 39, 70, 72, 77, 84), of soils and geothermal settings at a pH of ∼4 (55, 68), of metal-contaminated estuaries at pH 6.8 to 7.2 (65), and of hypersaline lakes at pH 7.5 (56) further outline the distribution and tolerance of specific groups and species of SRB under geochemically stringent conditions. Other findings point toward the existence of deltaproteobacteria in environments at a pH of ∼1 (10), although it is unknown if these include SRB. SRB diversity in salt marshes under long-term contamination by AMD has not been well investigated. Such studies may provide useful information for bioremediation projects in estuarine environments, as well as general insights into relationships between SRB physiology and the geochemistry of AMD.We studied the diversity of SRB, based on phylogenetic analysis of recovered DsrAB gene sequences (∼1.9 kb), in natural salt marsh sediments of the San Francisco Bay impacted by AMD for over 100 years. Sulfur isotope ratio and concentration measurements of pore water sulfate and metal sulfide minerals provided information about the spatial and temporal extent of active bacterial sulfate reduction (BSR) in sediment cores taken from specific sites along an AMD flow path. Collectively, the results revealed a tidal marsh system characterized by rapidly cycling bacterial sulfate reduction and sulfide reoxidation associated with oscillating tidal inundation and groundwater infiltration.  相似文献   

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Bacteria are recognized as an important part of the total biology of shallow-water corals. Studies of shallow-water corals suggest that associated bacteria may benefit the corals by cycling carbon, fixing nitrogen, chelating iron, and producing antibiotics that protect the coral from other microbes. Cold-water or deep-sea corals have a fundamentally different ecology due to their adaptation to cold, dark, high-pressure environments and as such have novel microbiota. The goal of this study was to characterize the microbial associates of Lophelia pertusa in the northeastern Gulf of Mexico. This is the first study to collect the coral samples in individual insulated containers and to preserve coral samples at depth in an effort to minimize thermal shock and evaluate the effects of environmental gradients on the microbial diversity of samples. Molecular analysis of bacterial diversity showed a marked difference between the two study sites, Viosca Knoll 906/862 (VK906/862) and Viosca Knoll 826 (VK826). The bacterial communities from VK826 were dominated by a variety of unknown mycoplasmal members of the Tenericutes and Bacteroidetes, whereas the libraries from VK906/862 were dominated by members of the Proteobacteria. In addition to novel sequences, the 16S rRNA gene clone libraries revealed many bacterial sequences in common between Gulf of Mexico Lophelia corals and Norwegian fjord Lophelia corals, as well as shallow-water corals. Two Lophelia-specific bacterial groups were identified: a cluster of gammaproteobacteria related to sulfide-oxidizing gill symbionts of seep clams and a group of Mycoplasma spp. The presence of these groups in both Gulf and Norwegian Lophelia corals indicates that in spite of the geographic heterogeneity observed in Lophelia-associated bacterial communities, there are Lophelia-specific microbes.Cold-water and deep-sea corals have become a topic of interest due to conservation concerns over the impacts of trawling, exploration for oil and gas, and climate change (51, 52). Although the existence of these corals has been known since the 1800s, our knowledge of their distribution, ecology, and biology is limited due to the technical difficulties of studying them. Lophelia pertusa is a globally distributed cold-water scleractinian coral (53). In the Gulf of Mexico, Lophelia reefs occur primarily along the continental shelf break (300- to 500-m depth), providing an important complex habitat for a wide variety of fishes, crustaceans, and other invertebrates living below the photic zone (48).The microbial ecology of cold-water corals in deep water is fundamentally different from that of shallow-water corals due to the ambient environmental parameters (e.g., darkness, low temperature, and increased pressure) and the absence of symbiotic zooxanthellae. A few studies have begun to address the microbial associates of deep-sea corals, focusing on octocorals (9, 44) and on L. pertusa (27, 41, 42, 57, 72). To date, all the Lophelia studies have been conducted on the eastern side of the Atlantic: the Mediterranean basin (72), Mingulay Bay, Scotland (27), and Norwegian fjords (41, 42, 57). These studies have confirmed that the Lophelia-associated bacterial community is distinct from that of the surrounding seawater and sediments (27, 42, 57, 72). A variety of community profile methods (automated rRNA intergenic spacer analysis, terminal restriction fragment length polymorphism, and denaturing gradient gel electrophoresis [DGGE]) were used to demonstrate differences between samples within a geographic area, suggesting that the Lophelia-associated microbial community varies depending on regional environmental factors (27, 42, 57). Sequencing of 16S rRNA genes was done in only two studies, and there was no overlap between their data (42, 72). However, different methods of collection, extraction, amplification, and sequencing were employed, so the lack of commonality may be due to methodology rather than biogeography.Methodology is a concern, particularly the care with which samples need to be collected for microbial ecology studies. Deep-sea coral samples are typically collected by a trawl, net, or dredge or by a submersible/remotely operated vehicle (ROV). With these methods, many corals may be combined in a single container, which is not acceptable for microbiological studies because the microbial community of one coral could contaminate that of the other. Similarly, contact with sediment, other invertebrates, mobile fauna, or water masses between the collection point and the surface could contaminate the coral samples. Unlike the case with the northeastern Atlantic and Norwegian fjords, the temperature and salinity gradients in the Gulf of Mexico during the warm months of the year can be considerable. In the case of the Viosca Knoll sites, the bottom temperature was 8 to 11°C, compared to a surface temperature of ≥30°C. Coral samples collected in uninsulated containers in this area have been observed to be affected (e.g., polyps retracted and copious stress mucus production) compared to those in insulated containers. Viosca Knoll is also impacted by the Mississippi River plume. The surface waters at these sites were turbid and green and had a salinity of 30 practical salinity units (psu), but below the plume the waters were clear and had a salinity of 35 psu. With this in mind, we designed a sampling container that would protect the coral samples from dramatic changes in temperature and salinity by sealing them in individual insulated compartments (see Fig. S1 in the supplemental material). However, the question remained whether environmental gradients in light and pressure would have an effect on the microbial diversity of the samples. To address this question, each sample was collected in duplicate: one piece was sealed in a compartment alive, and a replicate piece was sealed in another compartment and preserved at depth with a fixative solution. Both sample types (“live” versus “fixed”) were sealed and insulated, so temperature and salinity gradients did not affect them; live samples were subject to gradients in light and pressure, while fixed samples were not.The main objective of this study was to characterize the bacterial associates of Lophelia pertusa from two sites in the northern Gulf of Mexico. Comparing multiple individual colonies from two geographic locations in the Gulf to each other and to bacterial data from Lophelia samples on the eastern side of the Atlantic will clarify whether Lophelia has a species-specific bacterial community, as has been described for shallow-water corals (49, 55). The results of this study will also better define the total microbial diversity associated with this cold-water coral. A specialized sampling device (see Fig. S1 in the supplemental material) was designed to minimize contamination and thermal shock and to allow the introduction of preservative at depth to determine if environmental gradients were affecting microbial diversity during sampling.  相似文献   

17.
Methanogens are of great importance in carbon cycling and alternative energy production, but quantitation with culture-based methods is time-consuming and biased against methanogen groups that are difficult to cultivate in a laboratory. For these reasons, methanogens are typically studied through culture-independent molecular techniques. We developed a SYBR green I quantitative PCR (qPCR) assay to quantify total numbers of methyl coenzyme M reductase α-subunit (mcrA) genes. TaqMan probes were also designed to target nine different phylogenetic groups of methanogens in qPCR assays. Total mcrA and mcrA levels of different methanogen phylogenetic groups were determined from six samples: four samples from anaerobic digesters used to treat either primarily cow or pig manure and two aliquots from an acidic peat sample stored at 4°C or 20°C. Only members of the Methanosaetaceae, Methanosarcina, Methanobacteriaceae, and Methanocorpusculaceae and Fen cluster were detected in the environmental samples. The three samples obtained from cow manure digesters were dominated by members of the genus Methanosarcina, whereas the sample from the pig manure digester contained detectable levels of only members of the Methanobacteriaceae. The acidic peat samples were dominated by both Methanosarcina spp. and members of the Fen cluster. In two of the manure digester samples only one methanogen group was detected, but in both of the acidic peat samples and two of the manure digester samples, multiple methanogen groups were detected. The TaqMan qPCR assays were successfully able to determine the environmental abundance of different phylogenetic groups of methanogens, including several groups with few or no cultivated members.Methanogens are integral to carbon cycling, catalyzing the production of methane and carbon dioxide, both potent greenhouse gases, during organic matter degradation in anaerobic soils and sediment (8). Methanogens are widespread in anaerobic environments, including tundra (36), freshwater lake and wetland sediments (9, 12), estuarine and marine sediments (2), acidic peatlands (4, 14), rice field soil (10, 16), animal guts (41), landfills (30), and anaerobic digesters treating animal manure (1), food processing wastewater (27), and municipal wastewater and solid waste (37, 57). Methane produced in anaerobic digesters may be captured and used for energy production, thus offsetting some or all of the cost of operation and reducing the global warming potential of methane release to the atmosphere.Methanogens are difficult to study through culture-based methods, and therefore many researchers have instead used culture-independent techniques to study methanogen populations. The 16S rRNA gene is the most widely used target for gene surveys, and a number of primers and probes have been developed to target methanogen groups (9, 11, 31, 36, 38, 40, 46, 48, 57). To eliminate potential problems with nonspecific amplification, some researchers have developed primers for the gene sequence of the α-subunit of the methyl coenzyme M reductase (mcrA) (17, 30, 49). The Mcr is exclusive to the methanogens with the exception of the methane-oxidizing Archaea (18) and shows mostly congruent phylogeny to the 16S rRNA gene, allowing mcrA analysis to be used in conjunction with, or independently of, that of the 16S rRNA gene (3, 30, 49). A number of researchers have examined methanogen communities with mcrA and have found uncultured clades quite different in sequence from cultured methanogen representatives (9, 10, 12, 14, 17, 22, 28, 47).Previous studies described methanogen communities by quantitation of different clades through the use of rRNA-targeted or rRNA gene-targeted probes with techniques such as dot blot hybridization (1, 27, 37, 38, 48) and fluorescent in situ hybridization (11, 40, 44, 57). Real-time quantitative PCR (qPCR) is an alternate technique capable of determining the copy number of a particular gene present in the DNA extracted from an environmental sample. Only a few studies have used qPCR to quantitatively examine different clades within methanogen communities, and most of these studies have exclusively targeted the 16S rRNA gene (19, 41, 42, 54-56). Far fewer researchers have used qPCR to quantify methanogen clades by targeting the mcrA (21, 34, 45), and these studies were limited to only a few phylogenetic groups.In this paper we present a methodology for determining methanogen gene copy numbers through the use of qPCR targeting the mcrA. Methanogens were quantified in total using methanogen-specific primers in SYBR green assays and also as members of nine different phylogenetic groups using TaqMan probes targeting specific subsets of methanogens.  相似文献   

18.
Deleting individual genes for outer surface c-type cytochromes in Geobacter sulfurreducens partially inhibited the reduction of humic substances and anthraquinone-2,6,-disulfonate. Complete inhibition was obtained only when five of these genes were simultaneously deleted, suggesting that diverse outer surface cytochromes can contribute to the reduction of humic substances and other extracellular quinones.Humic substances can play an important role in the reduction of Fe(III), and possibly other metals, in sedimentary environments (6, 34). Diverse dissimilatory Fe(III)-reducing microorganisms (3, 5, 7, 9, 11, 19-22, 25) can transfer electrons onto the quinone moieties of humic substances (38) or the model compound anthraquinone-2,6-disulfonate (AQDS). Reduced humic substances or AQDS abiotically reduces Fe(III) to Fe(II), regenerating the quinone. Electron shuttling in this manner can greatly increase the rate of electron transfer to insoluble Fe(III) oxides, presumably because soluble quinone-containing molecules are more accessible for microbial reduction than insoluble Fe(III) oxides (19, 22). Thus, catalytic amounts of humic substances have the potential to dramatically influence rates of Fe(III) reduction in soils and sediments and can promote more rapid degradation of organic contaminants coupled to Fe(III) reduction (1, 2, 4, 10, 24).To our knowledge, the mechanisms by which Fe(III)-reducing microorganisms transfer electrons to humic substances have not been investigated previously for any microorganism. However, reduction of AQDS has been studied using Shewanella oneidensis (17, 40). Disruption of the gene for MtrB, an outer membrane protein required for proper localization of outer membrane cytochromes (31), inhibited reduction of AQDS, as did disruption of the gene for the outer membrane c-type cytochrome, MtrC (17). However, in each case inhibition was incomplete, and it was suggested that there was a possibility of some periplasmic reduction (17), which would be consistent with the ability of AQDS to enter the cell (40).The mechanisms for electron transfer to humic substances in Geobacter species are of interest because molecular studies have frequently demonstrated that Geobacter species are the predominant Fe(III)-reducing microorganisms in sedimentary environments in which Fe(III) reduction is an important process (references 20, 32, and 42 and references therein). Geobacter sulfurreducens has routinely been used for investigations of the physiology of Geobacter species because of the availability of its genome sequence (29), a genetic system (8), and a genome-scale metabolic model (26) has made it possible to take a systems biology approach to understanding the growth of this organism in sedimentary environments (23).  相似文献   

19.
Genome annotation of the chlorinated ethene-respiring “Dehalococcoides ethenogenes” strain 195 indicated the presence of a complete nitrogenase operon. Here, results from long-term growth experiments, gene expression, and 15N2-isotope measurements confirm that strain 195 is capable of fixing atmospheric dinitrogen when a defined fixed-nitrogen source such as ammonium is unavailable.“Dehalococcoides ethenogenes” strain 195 is the first isolated bacterium that is capable of reductively dechlorinating tetrachloroethene and trichloroethene (TCE) to vinyl chloride (VC) and ethene (22). Annotation of the 1.5-Mbp genome of strain 195 has identified 17 intact reductive dehalogenase (RDase) genes (25). The variety of RDases has essentially defined the metabolic capabilities of strain 195 and other Dehalococcoides strains for respiration of chlorinated ethenes (8, 9, 15, 23, 27) and other chlorinated compounds (1, 2, 6, 21), making them important participants in bioremediation processes (19). Expression of different putative RDase genes has been examined previously in pure culture (6) and in Dehalococcoides-containing enrichment cultures (3, 4, 13, 17, 24, 28).Genome annotation of strain 195 has revealed the presence of a nitrogenase-encoding operon (nif) (DET1151-58) typical of those found in anaerobes (25). According to the published genome annotations of four strains of Dehalococcoides, strain 195 is the only one that contains a nif operon (16, 25; Joint Genome Institute, 2009, Integrated Microbial Genomes system [www.jgi.doe.gov]). A nif operon closely related to that in strain 195 has also been identified in a mixed Dehalococcoides-containing community (29); thus, the nitrogen-fixing function might be present in other unsequenced strains of Dehalococcoides.Phylogenetically, the nitrogenase structural genes of strain 195 are clustered with diverse anaerobic Bacteria, including the molybdenum (Mo)-nitrogenase in Clostridium pasteurianum, as well as Archaea, including the Mo-nitrogenase in Methanosarcina barkeri (25, 30). In the genome of strain 195, the presence of an ABC transporter for molybdenum (DET1159-61) and a nifV gene (DET1614), which encodes homocitrate synthetase used in nitrogenase FeMo-cofactor biosynthesis, suggests that the nitrogenase is of the typical molybdenum-iron type (25). While strain 195 is the only sequenced Dehalococcoides isolate that contains a nif operon, Ju et al. (14) previously identified functional nifH genes in dechlorinating organisms from diverse genera such as Sulfurospirillum multivorans, Desulfovibrio dechloracetivorans, and Desulfomonile tiedjei.Aquifers containing groundwater contaminated with chlorinated ethenes can potentially be limited in nutrients. For example, at the Wurtsmith Air Force Base, the chlorinated ethene-contaminated groundwater was found to contain less than 0.09 mM of ammonia, prompting ammonium amendment (26). Little is currently known about the potential effects of nitrogen limitation on reductive dechlorination in the environment, and the demonstration of nitrogen fixation in strain 195 was previously hindered by the use of an undefined medium (21). Here, we present results demonstrating that strain 195 is capable of fixing atmospheric dinitrogen and the physiological implications of the stress caused by nitrogen limitation.  相似文献   

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