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通过转座子定向插入位点测序鉴定泰国伯克霍尔德菌在土壤中存活所需的基因。

Identification of genes required for soil survival in Burkholderia thailandensis by transposon-directed insertion site sequencing.

作者信息

Bishop A H, Rachwal P A

机构信息

Detection Department, Defence Science and Technology Laboratory, Porton Down, Salisbury, Wiltshire, SP4 0JQ, UK,

出版信息

Curr Microbiol. 2014 Jun;68(6):693-701. doi: 10.1007/s00284-014-0526-7. Epub 2014 Feb 2.

DOI:10.1007/s00284-014-0526-7
PMID:24488501
Abstract

Transposon-directed insertion site sequencing was used to identify genes required by Burkholderia thailandensis to survive in plant/soil microcosms. A total of 1,153 genetic loci fulfilled the criteria as being likely to encode survival characteristics. Of these, 203 (17.6 %) were associated with uptake and transport systems; 463 loci (40.1 %) coded for enzymatic properties, 99 of these (21.4 %) had reduction/oxidation functions; 117 (10.1 %) were gene regulation or sensory loci; 61 (5.3 %) encoded structural proteins found in the cell envelope or with enzymatic activities related to it, distinct from these, 46 (4.0 %) were involved in chemotaxis and flagellum, or pilus synthesis; 39 (3.4 %) were transposase enzymes or were bacteriophage-derived; and 30 (2.6 %) were involved in the production of antibiotics or siderophores. Two hundred and twenty genes (19.1 %) encoded hypothetical proteins or those of unknown function. Given the importance of motility and pilus formation in microcosm persistence the nature of the colonization of the rhizosphere was examined by confocal microscopy. Wild type B. thailandensis expressing red fluorescent protein was inoculated into microcosms. Even though the roots had been washed, the bacteria were still present but they were motile with no attachment having taken place, perhaps being retained in a biofilm.

摘要

转座子导向的插入位点测序被用于鉴定泰国伯克霍尔德菌在植物/土壤微观环境中生存所需的基因。共有1153个基因座符合可能编码生存特性的标准。其中,203个(17.6%)与摄取和运输系统相关;463个基因座(40.1%)编码酶的特性,其中99个(21.4%)具有还原/氧化功能;117个(10.1%)是基因调控或传感基因座;61个(5.3%)编码在细胞膜中发现的结构蛋白或与之相关的酶活性,除此之外,46个(4.0%)参与趋化作用、鞭毛或菌毛合成;39个(3.4%)是转座酶或来源于噬菌体;30个(2.6%)参与抗生素或铁载体的产生。220个基因(19.1%)编码假设的蛋白质或功能未知的蛋白质。鉴于运动性和菌毛形成在微观环境持久性中的重要性,通过共聚焦显微镜检查了根际定殖的性质。将表达红色荧光蛋白的野生型泰国伯克霍尔德菌接种到微观环境中。尽管根已被冲洗,但细菌仍然存在,但它们具有运动性,没有发生附着,可能保留在生物膜中。

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本文引用的文献

1
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Proc Natl Acad Sci U S A. 2012 Aug 7;109(32):13088-93. doi: 10.1073/pnas.1200791109. Epub 2012 Jul 5.
2
Structure and regulation of the type VI secretion system.VI 型分泌系统的结构与调控。
Annu Rev Microbiol. 2012;66:453-72. doi: 10.1146/annurev-micro-121809-151619. Epub 2012 Jun 28.
3
Out of the ground: aerial and exotic habitats of the melioidosis bacterium Burkholderia pseudomallei in grasses in Australia.
从土壤中冒出:澳大利亚草类中鼻疽伯克霍尔德菌的气生和异域生境。
Environ Microbiol. 2012 Aug;14(8):2058-70. doi: 10.1111/j.1462-2920.2011.02671.x. Epub 2011 Dec 19.
4
Evidence-based annotation of gene function in Shewanella oneidensis MR-1 using genome-wide fitness profiling across 121 conditions.使用 121 种条件下的全基因组适合度分析对 Shewanella oneidensis MR-1 中的基因功能进行基于证据的注释。
PLoS Genet. 2011 Nov;7(11):e1002385. doi: 10.1371/journal.pgen.1002385. Epub 2011 Nov 17.
5
Bioremediation approaches for organic pollutants: a critical perspective.生物修复有机污染物的方法:批判性视角。
Environ Int. 2011 Nov;37(8):1362-75. doi: 10.1016/j.envint.2011.06.003. Epub 2011 Jul 1.
6
Retrospective application of transposon-directed insertion site sequencing to a library of signature-tagged mini-Tn5Km2 mutants of Escherichia coli O157:H7 screened in cattle.经回溯分析,用转座子定向插入位点测序法对从牛体内筛选出的大肠杆菌 O157:H7 特征性标签微型Tn5Km2 突变体文库进行了研究。
J Bacteriol. 2011 Apr;193(7):1771-6. doi: 10.1128/JB.01292-10. Epub 2011 Jan 28.
7
Integrative genomics viewer.整合基因组浏览器。
Nat Biotechnol. 2011 Jan;29(1):24-6. doi: 10.1038/nbt.1754.
8
Methods for genetic manipulation of Burkholderia gladioli pathovar cocovenenans.唐菖蒲伯克霍尔德菌椰毒变种的基因操作方法。
BMC Res Notes. 2010 Nov 16;3:308. doi: 10.1186/1756-0500-3-308.
9
Roles of multiple acetoacetyl coenzyme A reductases in polyhydroxybutyrate biosynthesis in Ralstonia eutropha H16.多重乙酰乙酰辅酶 A 还原酶在 Ralstonia eutropha H16 聚羟基丁酸酯生物合成中的作用。
J Bacteriol. 2010 Oct;192(20):5319-28. doi: 10.1128/JB.00207-10. Epub 2010 Aug 20.
10
Simultaneous assay of every Salmonella Typhi gene using one million transposon mutants.利用一百万转座子突变体同时检测每一个伤寒沙门氏菌基因。
Genome Res. 2009 Dec;19(12):2308-16. doi: 10.1101/gr.097097.109. Epub 2009 Oct 13.