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991.
Recovery of transgenic plants by pollen-mediated transformation in <Emphasis Type="Italic">Brassica juncea</Emphasis> 总被引:1,自引:0,他引:1
The aroA-M1 encoding the mutant of 5-enolpyruvyl-shikimate-3-phosphate synthase (EPSPS) was introduced into the Brassica juncea genome by sonication-assisted, pollen-mediated transformation. The plasmid DNA and collected pollen grains were mixed in
0.3 mol/L sucrose solution and treated with mild ultrasonication. The treated pollen was then pollinated onto the oilseed
stigmas after the stamens were removed artificially. Putative transgenic plants were obtained by screening germinating seeds
on a medium containing glyphosate. Southern blot analysis of glyphosate-resistant plants indicated that the aroA-M1 gene had been integrated into the oilseed genome. Western blot analysis further confirmed that the EPSPS coded by aroA-M1 gene was expressed in transgenic plants. The transgenic plants exhibited increased resistance to glyphosate compared to untransformed
plants. Some of those transgenic plants had considerably high resistance to glyphosate. The genetic analysis of T1 progeny further confirmed that the inheritance of the introduced genes followed the Mendelian rules. The results indicated
that foreign genes can be transferred by pollen-mediated transformation combined with mild ultrasonication. 相似文献
992.
A thermophilic bacterial strain GXN151 which could degrade Avicel efficiently was isolated and identified as Bacillus licheniformis. A genomic library of GXN151 was constructed and two novel endoglucanase genes designated cel9A and cel12A were isolated by screening the library on carboxylmethyl cellulase indicator plates. The analysis of amino acid sequences deduced from the genes indicated that Cel9A consisted of a catalytic domain belonging to glycosyl hydrolase family 9, a linker domain, and a carbohydrate binding module family 3 from N-terminal to C-terminal; Cel12A had only one catalytic domain belonging to glycosyl hydrolase family 12. The combinations of Cel9A and Cel12A produced by the recombinant E. coli exhibited synergistic action against substrates of carboxylmethyl cellulose as well as Avicel. 相似文献
993.
Sediment quality criteria in use around the world 总被引:20,自引:0,他引:20
There have been numerous sediment quality guidelines (SQGs) developed during the past 20 years to assist regulators in dealing
with contaminated sediments. Unfortunately, most of these have been developed in North America. Traditionally, sediment contamination
was determined by assessing the bulk chemical concentrations of individual compounds and often comparing them with background
or reference values. Since the 1980s, SQGs have attempted to incorporate biological effects in their derivation approach.
These approaches can be categorized as empirical, frequency-based approaches to establish the relationship between sediment
contamination and toxic response, and theoretically based approaches that attempt to account for differences in bioavailability
through equilibrium partitioning (EqP) (i.e., using organic carbon or acid volatile sulfides). Some of these guidelines have
been adopted by various regulatory agencies in several countries and are being used as cleanup goals in remediation activities
and to identify priority polluted sites. The original SQGs, which compared bulk chemical concentrations to a reference or
to background, provided little insight into the ecosystem impact of sediment contaminants. Therefore, SQGs for individual
chemicals were developed that relied on field sediment chemistry paired with field or laboratory-based biological effects
data. Although some SQGs have been found to be relatively good predictors of significant site contamination, they also have
several limitations. False positive and false negative predictions are frequently in the 20% to 30% range for many chemicals
and higher for others. The guidelines are chemical specific and do not establish causality where chemical mixtures occur.
Equilibrium-based guidelines do not consider sediment ingestion as an exposure route. The guidelines do not consider spatial
and temporal variability, and they may not apply in dynamic or larger-grained sediments. Finally, sediment chemistry and bioavailability
are easily altered by sampling and subsequent manipulation processes, and therefore, measured SQGs may not reflect in situ
conditions. All the assessment tools provide useful information, but some (such as SQGs, laboratory toxicity and bioaccumulation,
and benthic indices) are prone to misinterpretation without the availability of specific in situ exposure and effects data.
SQGs should be used only in a “screening” manner or in a “weight-of-evidence” approach. Aquatic ecosystems (including sediments)
must be assessed in a “holistic” manner in which multiple components are assessed (e.g., habitat, hydrodynamics, resident
biota, toxicity, and physicochemistry, including SQGs) by using integrated approaches.
Received: December 26, 2000 / Accepted: December 28, 2001 相似文献
994.
Eutrophication assessment and bioremediation strategy in a marine fish cage culture area in Nansha Bay,China 总被引:3,自引:0,他引:3
On the basis of field data measured during four cruises from January to November 2007, variations in the characteristics of
dissolved inorganic nitrogen and phosphate were analyzed in Nansha marine fish cage culture area, Ningbo City, China. Dissolved
inorganic nitrogen (DIN) was selected as the parameter to balance seaweed absorption and fish DIN production. The contents
of DIN and phosphate varied with different seasons, and eutrophication index (E) value ranged from 2.41 to 15.99, indicating serious eutrophication conditions; the annual average value of N/P of 32.95
indicates a nitrogen surplus in this system. The eutrophication condition in Nansha Bay was mainly caused by the fish cage
culture activities. Based on their biological characteristics, Laminaria and Gracilaria were selected as the bioremediation species in winter and spring and summer and autumn, respectively. The optimal co-cultivation
proportion of fish cage to Laminaria and Gracilaria in this bay was 1 cage, 450 m2 and one cage, 690 m2, respectively. 相似文献
995.
Yun Sook Kim Dae-Sung Lee Seong-Yun Jeong Woe Jae Lee Myung-Suk Lee 《Journal of microbiology (Seoul, Korea)》2009,47(1):9-18
A bacterial strain named AB-4 showing algicidal activity against Chattonella marina was isolated from coastal water of ULjin, Republic of Korea. The isolated strain was identified as Bacillus sp. by culture morphology, biochemical reactions, and homology research based on 16S rDNA. The bacterial culture led to the
lysis of algal cells, suggesting that the isolated strain produced a latent algal-lytic compound. Amongst changes in algicidal
activity by different culture filtrate volumes, the 10% (100 μl/ml) concentration showed the biggest change in algicidal activity;
there, estimated algicidal activity was 95%. The swimming movements of Chattonella marina cells were inhibited because of treatment of the bacterial culture; subsequently, Chattonella marina cells became swollen and rounded. With longer exposure time, algal cells were disrupted and cellular components lost their
integrity and decomposed. The released algicide(s) were heat-tolerant and stable in pH variations, except pH 3, 4, and 5.
Culture filtrate of Bacillus sp. AB-4 was toxic against harmful algae bloom (HAB) species and nontoxic against livefood organisms. Bacillus sp. AB-4 showed comparatively strong activity against Akashiwo sanguinea, Fibriocapsa japonica, Heterosigma akashiwo, and Scrippsiella trochoidea. These results suggest that the algicidal activity of Bacillus sp. AB-4 is potentially useful for controlling outbreaks of Chattonella marina. 相似文献
996.
MCPIP1 ribonuclease antagonizes dicer and terminates microRNA biogenesis through precursor microRNA degradation 总被引:2,自引:0,他引:2
Suzuki HI Arase M Matsuyama H Choi YL Ueno T Mano H Sugimoto K Miyazono K 《Molecular cell》2011,44(3):424-436
MicroRNAs (miRNAs) are versatile regulators of gene expression and undergo complex maturation processes. However, the mechanism(s) stabilizing or reducing these small RNAs remains poorly understood. Here we identify mammalian immune regulator MCPIP1 (Zc3h12a) ribonuclease as a broad suppressor of miRNA activity and biogenesis, which counteracts Dicer, a central ribonuclease in miRNA processing. MCPIP1 suppresses miRNA biosynthesis via cleavage of the terminal loops of precursor miRNAs (pre-miRNAs). MCPIP1 also carries a vertebrate-specific oligomerization domain important for pre-miRNA recognition, indicating its recent evolution. Furthermore, we observed potential antagonism between MCPIP1 and Dicer function in human cancer and found a regulatory role of MCPIP1 in the signaling axis comprising miR-155 and its target c-Maf. These results collectively suggest that the balance between processing and destroying ribonucleases modulates miRNA biogenesis and potentially affects pathological miRNA dysregulation. The presence of this abortive processing machinery and diversity of MCPIP1-related genes may imply a dynamic evolutional transition of the RNA silencing system. 相似文献
997.
Coppoolse ER de Vroomen MJ van Gennip F Hersmus BJ van Haaren MJ 《Plant molecular biology》2005,58(5):687-698
Cre/lox recombination in vivo has become an important tool to induce chromosomal rearrangements like deletions. Using a combination of Ds transposition and Cre/lox recombination in two independent experiments on chromosomes 6 and 7 of tomato, two sets of somatic deletions up to a size of 200 kb were obtained. The efficiency of somatic deletion decreased with increasing deletion size. The largest germinally transmitted deletion had a size of only 55 kb. The results show that Cre-mediated deletion in somatic cells is less efficient when the lox sites are separated over larger distances. A further drop of the deletion efficiency after germinal transmission of the larger deletions can be explained by the probable loss of genes that are of vital importance to gametophyte function. Plasmid rescue of an 8.4 kb circularised deleted DNA showed that the Cre-mediated deletion takes place in tomato as expected. Since the circular Cre-deleted DNA could only be PCR amplified in plant cells where the deletion was not complete, the double-stranded DNA circle is assumed to be instable. 相似文献
998.
Background
Fructans – β-D-fructofuranosyl polymers with a sucrose starter unit – constitute a carbohydrate reservoir synthesised by a considerable number of bacteria and plant species. Biosynthesis of levan (αGlc(1–2)βFru [(2–6)βFru]n), an abundant form of bacterial fructan, is catalysed by levansucrase (sucrose:2,6-β-D-fructan-6-β-D-fructosyl transferase), utilizing sucrose as the sole substrate. Previously, we described the tertiary structure of Bacillus subtilis levansucrase in the ligand-free and sucrose-bound forms, establishing the mechanistic roles of three invariant carboxylate side chains, Asp86, Asp247 and Glu342, which are central to the double displacement reaction mechanism of fructosyl transfer. Still, the structural determinants of the fructosyl transfer reaction thus far have been only partially defined. 相似文献999.
Melissa K. Wilson Alison B. Lane Bibiana F. Law William G. Miller Lynn A. Joens Michael E. Konkel Bryan A. White 《Microbial ecology》2009,58(4):843-855
Campylobacter jejuni is one of the leading bacterial causes of food-borne illness in the USA. Molecular typing methods are often used in food
safety for identifying sources of infection and pathways of transmission. Moreover, the identification of genetically related
isolates (i.e., clades) may facilitate the development of intervention strategies for control and prevention of food-borne
diseases. We analyzed the pan genome (i.e., core and variable genes) of 63 C. jejuni isolates recovered from chickens raised in conventional, organic, and free-range poultry flocks to gain insight into the
genetic diversity of C. jejuni isolates recovered from different environments. We assessed the discriminatory power of three genotyping methods [i.e., pulsed-field
gel electrophoresis (PFGE), multilocus sequence typing (MLST), and repetitive extragenic palindromic polymerase chain reaction
(rep-PCR)]. The rep-PCR fingerprint was generated by determining the presence of repetitive sequences that are interspersed throughout
the genome via repetitive extragenic palindromic PCR, enterobacterial repetitive intergenic consensus sequence PCR (ERIC-PCR),
and BOX element PCR (BOX-PCR) and combining the data to form a composite fingerprint. The genetic fingerprints were subjected
to computer-assisted pattern analysis. Comparison of the three genotypic methods revealed that repREB-PCR showed greater discriminatory
power than PFGE and MLST. ERIC-PCR and BOX-PCR yielded the highest number of PCR products and greatest reproducibility. Regardless
of the genotyping method, C. jejuni isolates recovered from chickens reared in conventional, organic, and free-range environments all exhibit a high level of
genotypic diversity. 相似文献
1000.
d-lactic acid is a versatile and important industrial chemical that can be applied in the synthesis of thermal-resistant poly-lactic acid. Biosynthesis of d-lactic acid can be achieved by a variety of microorganisms, including lactic acid bacteria, yeast, and fungi; however, the final product yield, optical purity, and the utilization of both glucose and xylose are restricted. Consequently, engineered microbial systems are essential to attain high titer, productivity, and complete utilization of sugars. Herein, we critically evaluate the promising wild-type microorganisms, as well as genetically modified microorganisms to produce enantiomerically pure d-lactic acid, particularly from renewable lignocellulosic biomass. In addition, innovative bioreactor operation, metabolic flux analysis, and recent genetic engineering methods for targeted microbial d-lactic acid synthesis will be discussed. 相似文献