近三年微生物多样性研究进展（英文）

综述了近三年来微生物多样性研究领域的研究进展,对不同年份相关文章的数量、不同数据库中相关文章的数量以及作者倾向于选择的不同微生物多样性研究对象的相关文章的数量进行了统计。文中针对微生物多样性研究领域作者选择的不同研究重点进行了分类和归纳,并且对其研究结果进行了简要介绍。为研究者提供了近年来微生物多样性研究的大致框架,为研究对象的选择和研究重点的设定提供依据。     

非培养生物方法在堆肥微生物生态中的应用展望

微生物是堆肥化处理研究中被重点关注的因素,但大部分堆肥微生物都处于存活不可培养状态,使得了解堆肥过程中微生物实际群落结构比较困难。非培养生物方法的快速发展,为解决这一难题提供了技术依据。分别就生物化学,分子生物学,生理学中不依赖于传统培养技术的代表方法PLFA谱图分析法、FISH技术、Biolog微量板分析法进行了介绍,综述了3类方法的组合应用以及在堆肥微生物生态中的应用展望。     

红枣贮藏期果面微生物对碳源的利用及主成分分析

Biolog方法就是微生物在利用碳源过程中产生的自由电子, 与四唑盐染料发生还原显色反应, 颜色的深浅可以反映微生物对碳源的利用程度。采用Biolog方法, 研究红枣贮藏期果面微生物对FF和ECO微孔板上碳源的利用情况, 进行主成分分析(Principal component analysis, PCA)。羧酸类、吐温类、碳水化合物、酯类、氨基酸类及胺类碳源是红枣贮藏期果面微生物群落在FF和ECO微孔板上利用的主要碳源。随着贮藏时间的延长, 红枣果面微生物对碳源的利用情况差异较大, 用保鲜剂处理过的红枣果面微生物对碳源的利用远远低于未处理的红枣果面微生物, 而且贮藏时间越长, 果面微生物对碳源的利用程度越高。利用ECO微孔板上31种碳源作PCA, 第一主成分特征值的贡献率为78.54%, 第二主成分特征值的贡献率为19.06%。     

土壤微生物多样性研究方法

概述了研究土壤微生物多样性的主要方法．传统上,土壤微生物群落的分析依赖于培养技术,使用各种培养基最大限度地培养各种微生物群体,但仍只能培养和分离出一小部分土壤微生物群落．使用Biolog分析、磷脂脂肪酸分析和核酸分析等方法,可研究和表征那些现在还不能够被培养的土壤微生物。从而获取关于土壤微生物群落多样性的更多和更完整的信息．     

有机物料种类及腐熟水平对土壤微生物群落的影响

应用Biolog方法研究了温室盆栽番茄条件下,施用不同种类及不同腐熟水平的有机物料对土壤微生物群落的影响,施用有机物料60d后取土分析土壤微生物群落多样性及土壤微生物对Biolog微平板中胺、氨基酸、糖、羧酸、聚合物和其它类碳源的利用情况,结果表明,施用有机物料可提高土壤微生物群落多样性,施用新鲜酒糟的多样性指数略高于施用腐熟10d酒糟,牛粪不同腐熟水平对多样性影响显著,且对多样性具有正向或负向的影响;对照和施用酒糟的土壤微生物对聚合物的利用率高于施用牛粪处理,施用新鲜物料处理的土壤微生物对聚合物的利用率高于施用腐熟物料处理。     

大庆盐碱地九种植物根际土壤微生物群落结构及功能多样性

盐碱土是陆地表面生态脆弱区域。它与荒漠化过程相伴而生,不但造成了资源的破坏、农业生产的巨大损失,而且还对生物圈和生态环境构成威胁。研究盐碱地植物根际土壤微生物群落的多样性,对于盐碱土壤的植被恢复和生态重建具有重要意义。运用PCR-DGGE技术和Biolog微平板法,对大庆盐碱地9种不同植物根际土壤微生物结构和功能的多样性进行了分析。结果表明,不同植物根际土壤微生物组成不同,同一科的植物具有相似的微生物组成。对11个克隆进行了序列测定,发现这一地区植物根际优势微生物菌群为变形菌门(Proteobacteria)和酸杆菌门(Acidobacteria)。利用Biolog微平板法分析了微生物群落功能多样性。结果表明,不同植物根际土壤细菌群落对底物碳源的代谢特征存在着一定的差异,其中豆科的野大豆根际土壤细菌对底物碳源的代谢能力最强。     

伏曲酵母菌的分类鉴定及来源分析的研究

目的:统计分析酵母菌的来源,为大曲微生物物种及其来源变化提供基础资料.方法:利用Biolog微生物自动分析系统进行精确鉴定,并通过统计分析得出微生物菌种的来源.结果:从伏曲样品中分离纯化出7株酵母菌J-1,2,3,4,5,6,7,利用Biolog微生物自动鉴定系统进行鉴定,确定其分别为白吉利丝孢酵母A、无名假丝酵母菌、汉逊德巴利酵母C、海隐球酵母菌、东方伊萨酵母菌、解脂耶罗威亚酵母菌、皱落假丝酵母菌.这些物种主要来源于原料本身和空气,原料为了人室大曲提供了J-1,2,3三种酵母菌,其比例为25.45%、19.23%和7.5%.结论:空气巾含有大曲中所有的酵母菌的种类,曲房空气中的酵母菌数量和种类均较多.     

盐爪爪根部微生物分布特征及盐浓度对碳源代谢分析的影响

【背景】耐盐植物盐爪爪广泛分布于盐碱荒漠区域,其根际存在明显的盐离子富集,形成"盐岛效应",研究此过程中微生物如何演替和适应,对揭示盐爪爪根际微生物的分布及其耐盐特性、"盐岛"的形成具有重要科学意义。【目的】揭示盐爪爪根际、根区及其周围环境土壤中微生物分布特征,确定不同盐浓度处理对根际微生物Biolog Eco微平板碳源代谢多样性的影响。【方法】采用Biolog Eco微平板技术,对采自新疆和硕地区的盐爪爪根际、根区和环境土壤微生物碳源利用情况进行分析,并采用不同浓度NaCl溶液对盐爪爪根际土壤样品进行稀释加样,评估盐浓度对根际微生物活性及多样性分析的影响。【结果】样品微生物代谢活性总体呈现根际根区环境的趋势;随着与根部距离的增加,样品中利用氨基酸、胺类碳源微生物所占比例明显降低,而利用吐温和肝糖等多聚化合物类碳源微生物所占比例明显增加;多样性分析表明,随着与根部距离的增加,Shannon指数(H)随之降低且存在明显差异。不同浓度NaCl溶液对采用BiologEco微平板技术分析盐爪爪根际微生物的代谢活性和代谢多样性有着明显的影响,其中采用5%NaCl溶液作为稀释加样液的根际微生物活性最高。【结论】盐爪爪根部微生物组成和分布有着明显的演变规律,且采用Biolog Eco微平板技术分析微生物代谢多样性时需进行培养条件的优化。     

分子生物学方法在环境微生物生态学中的应用研究进展

随着分子生物学方法的不断发展和改进,微生物在生态系统中的作用被更好的挖掘出来。目前快速发展的先进的分子生物学技术,已经开始应用于分析环境微生物的多样性、微生物的生物地理学及微生物对气候变化的响应等。一般环境微生物的研究目标主要有3个,即确定微生物的种类和多样性、微生物的功能或潜在作用及在特定时间点活跃的微生物等。然而,现有微生物的研究方法复杂多样,容易给研究者在方法的选择上带来困惑。将从微生物的多样性和功能研究两个方面介绍和分析相应的分子生物学方法,尤其是近年来快速发展的高通量测序、宏组学和单细胞水平研究方法(如纳米二次离子质谱与荧光原位杂交相结合的方法)等新技术及其应用情况,以期为研究者选择合适的研究方法进行环境微生物的研究提供依据。     

红枣贮藏期果面微生物功能多样性研究

摘要：【目的】了解果品微生物功能多样性信息,为红枣贮藏期贮藏病害的防控提供技术支撑,同时希望为果品果面微生物多样性的研究提供新的方法。【方法】采用Biolog方法研究了红枣贮藏期果品果面微生物群落结构功能多样性。【结果】红枣在不同贮藏时间内果面微生物群落的功能多样性差异很大,贮藏时间越长微生物越丰富,对不同碳源的利用程度越高;采用保鲜剂处理后红枣果面微生物群落的多样性、均匀度指数和AWCD 均显著低于未作任何处理的红枣果面微生物。四种不同处理的红枣果面微生物的特征碳源主要有六类：碳水化合物类、羧酸类、聚合     

土壤样品长期保存对微生物群落代谢活性和功能类群的影响

【目的】评估土壤长期保存(4个月)对土壤微生物群落代谢活性的影响。【方法】采用Biolog? EcoPlateTM生态板研究4 °C风干保存和?20 °C低温冻存的农田土壤和森林土壤中微生物群落的碳源利用模式。【结果】与新鲜土壤样品相比,长期保存的土壤样品的微生物群落对碳源的利用能力大大降低,其多样性、均匀度和Simpson指数均降低;风干保存和低温冻存两者对土壤微生物的碳源利用的影响没有显著差异;除风干保存的土壤样品中利用多聚物类的微生物类群的代谢活性外,两种保存方法显著降低微生物群落的代谢活性,降低幅度为54.5%–99.8%。【结论】长期保存土壤可能会导致对微生物群落信息的低估,土壤微生物代谢活性研究的最佳样品为新鲜 土壤。     

Functional Diversity of Bacterioplankton in Three North Florida Freshwater Lakes over an Annual Cycle

The phylogenetic diversity of freshwater bacterioplankton is widely known; however, there is minimal information on the functional diversity of the bacterial communities in these systems. Understanding the functional diversity of freshwater bacterial communities is important because heterotrophic bacteria can be impacted by anthropogenic perturbation, which in turn can alter biogeochemical cycling. The objective of this study was to use Biolog EcoPlates to acquire spatial and temporal community-level physiological profiles (CLPPs) for three freshwater lakes of different trophic levels and to assess the phylogenetic affiliation of the bacteria responsible for utilizing the various carbon guilds within them by denaturing gradient gel electrophoresis (DGGE). CLPP results showed that bacterial communities utilized the carbon guilds similarly between sites within the three lakes. However, when the metabolic profile of each lake was compared, Lake Bradford and Moore Lake were more similar to one another than to Lake Munson, the eutrophic lake. Additionally, although the bacteria that utilized the five carbon guilds included representatives from the classes α-, β-, γ-Proteobacteria, Flavobacteria and Sphingobacteria, Lake Munson had the largest number of Flavobacteria and γ-Proteobacteria in comparison to Moore Lake and Lake Bradford. Overall, Biolog analysis was useful in identifying differences in the functional diversity of bacterial communities between lakes of different trophic statuses and can be used as a tool to assess ecosystem health.     

黄瓜苗根围拮抗细菌X3的分子鉴定

采用生理生化、Biolog和16S rDNA分子鉴定3种不同方法,对抑制黄瓜苗期猝倒病病原真菌的细菌菌株X3进行了鉴定．生理生化鉴定显示该菌株为Pseudomonas aeruginosa;而Biolog鉴定显示其为P．spinosa;进一步对该菌株作16S rDNA基因的测定与分析,表明其与已报道的P．aeruginosa 16S rDNA具有93．7％的同源性,二者在所建系统发育树中处于同一分枝,据此确定该菌株为P．aeruginosa。     

Evaluation of phenotypic and molecular typing techniques for determining diversity in Erwinia carotovora subspp. atroseptica

A number of phenotypic and molecular fingerprinting techniques, including physiological profiling (Biolog), restriction fragment length polymorphism (RFLP), enterobacterial repetitive intergenic consensus (ERIC) and a phage typing system, were evaluated for their ability to differentiate between 60 strains of Erwinia carotovora ssp. atroseptica (Eca) from eight west European countries. These techniques were compared with other fingerprinting techniques, random amplified polymorphic DNA (RAPD) and Ouchterlony double diffusion (ODD), previously used to type this pathogen. Where possible, data were represented as dendrograms and groups/subgroups of strains identified. Simpson's index of diversity (Simpson's D) was used to compare groupings obtained with the different techniques which, with the exception of Biolog, gave values of 0.46 (RFLP), 0. 39 (ERIC), 0.83 (phage typing), 0.82 (RAPD) and 0.26 (ODD). Of the techniques tested, phage typing showed the highest level of diversity within Eca, and this technique will now form the basis of studies into the epidemiology of blackleg disease.     

Use of metabolic and molecular methods for the identification of a Bacillus strain isolated from paper affected by foxing

Foxing of paper is a deterioration phenomenon occurring in the form of brown-yellowish spots, the abiotic and/or biotic causes of which are not yet completely understood. Nevertheless, microbiological infection has been recognized that may contribute to paper damage and therefore it becomes important to know the taxonomic position and the degradative activity of the potential infectious biological agents which mostly are fungi, but also bacteria and yeasts. A cellulolytic bacterial strain isolated from a foxed paper sample exhibited morphological and physiological characteristics of the Bacillus genus. To study its taxonomic position, different identification methods were used: the Biolog system, the direct amplified polymorphic DNA-polymerase chain reaction analysis (DAPD-PCR) and the partial sequencing of the 16S rDNA gene. Biolog system and partial sequencing of 16S rDNA gene assigned the strain to the Paenibacillus polymyxa species. DAPD-PCR analysis indicated a high similarity with Bacillus circulans, by comparing the isolated strain with some closely related Bacillus species.     

Changes in the potential functional diversity of the bacterial community in biofilters

The bacterial community structure in a biofilter treating ethanol was investigated using community level physiological profiling. Laboratory scale biofilters of two sizes (5 or 11.5 cm internal diameter with 30 or 67 cm packed height, respectively) were packed with compost and a humidified airstream loaded with ethanol passed through them. Good removal efficiencies (82–100%) and elimination capacities (49–205 g ethanol m^− 3 h^− 1) were observed in all units. Compost packing media samples were extracted and the community level physiological profiles assayed using Biolog Ecoplates. The community structure was found to be similar over a range of a few centimetres. No differences were observed between sample sizes of 0.5–1 and 6 g, and therefore, the smaller sample size (typical of that used in previous studies) is appropriate for use in the future. Two studies of parallel systems showed that the community structure diverged during the acclimation period (10 days) in one pair, but in another pair, no divergence was observed and a similar shift in community profile was observed in both units between 25 and 40 days of operation. Community level physiological profiling with Biolog Ecoplates is a useful method for detecting differences between and changes within the bacterial communities in biofilters.     

Application of carbon source utilization patterns to measure the metabolic similarity of complex dental plaque biofilm microcosms

Biolog technology was applied to measure the metabolic similarity of plaque biofilm microcosms, which model the complex properties of dental plaque in vivo. The choice of Biolog plate, incubation time, and incubation conditions strongly influenced utilization profiles. For plaque biofilm microcosms, Biolog GP2 plates incubated anaerobically in an H2-free atmosphere gave the clearest profile. To test the application of the Biolog GP2 assay, plaque microcosms were developed under different nutrient conditions in which the frequency of sucrose application was varied. Cluster analysis of Biolog GP2 data from 10 microcosm biofilms correlated with sucrose frequency. Aciduric bacteria (Streptococcus mutans plus lactobacilli) predominated in the plaques receiving high-frequency sucrose applications. Agreement between the Biolog GP2 groupings with nutrient and compositional changes suggests that Biolog analysis is a valuable technique for analyzing the metabolic similarity of dental plaque biofilm microcosms and other high-nutrient or predominantly anaerobic ecosystems.     

Genetic and Physiological Characterization of the Intestinal Bacterial Microbiota of Bluegill (Lepomis macrochirus) with Three Different Feeding Habits

Bluegill (Lepomis macrochirus) in Lake Biwa, Japan, feed on benthic invertebrates (benthivorous type), aquatic plants (herbivorous type), and zooplankton (planktivorous type). To evaluate the effect of food on intestinal bacterial microbiota, we characterized and compared the intestinal microbiota of these three types of bluegill in terms of community-level physiological profile (CLPP) and genetic structure. The CLPP was analyzed using Biolog MicroPlates (Biolog, Inc., Hayward, CA, USA), and multivariate analysis of variance revealed that the CLPP of intestinal microbiota differed significantly between any pairs of the three types of bluegill. The genetic profiles were analyzed by temperature gradient gel electrophoresis of polymerase chain reaction (PCR)-amplified 16S rDNA fragments, and multidimensional scaling indicated the existence of specific intestinal bacterial structures for both the benthivorous and the planktivorous types. These results suggest that the host's feeding habit can be one factor controlling the intestinal microbiota of fish in the natural environment.     

Application of Carbon Source Utilization Patterns To Measure the Metabolic Similarity of Complex Dental Plaque Biofilm Microcosms

Biolog technology was applied to measure the metabolic similarity of plaque biofilm microcosms, which model the complex properties of dental plaque in vivo. The choice of Biolog plate, incubation time, and incubation conditions strongly influenced utilization profiles. For plaque biofilm microcosms, Biolog GP2 plates incubated anaerobically in an H₂-free atmosphere gave the clearest profile. To test the application of the Biolog GP2 assay, plaque microcosms were developed under different nutrient conditions in which the frequency of sucrose application was varied. Cluster analysis of Biolog GP2 data from 10 microcosm biofilms correlated with sucrose frequency. Aciduric bacteria (Streptococcus mutans plus lactobacilli) predominated in the plaques receiving high-frequency sucrose applications. Agreement between the Biolog GP2 groupings with nutrient and compositional changes suggests that Biolog analysis is a valuable technique for analyzing the metabolic similarity of dental plaque biofilm microcosms and other high-nutrient or predominantly anaerobic ecosystems.