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Culturing uncultured environmental microorganisms.

机译:培养未培养的环境微生物。

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摘要

Research on natural environments, over the last decade, is replete with microbial diversity studies that used culture-independent approaches. The cloning and sequencing of the 16S rRNA genes has been the driving force in the expansion of awareness about the great diversity of previously undiscovered microorganisms. Well-known uncultured groups of microorganisms are numerous, and half of the known phylogenetic divisions of bacteria are not represented in any culture collection. It is no longer assumed that cultures acquired from an environment represent the dominant or physiologically important organisms from that environment. A high throughput culturing (HTC) technique was developed in an attempt to bring into culture some of these widespread and uncultured microorganisms. Over the course of 3 years, 2,484 culturing attempts were screened for microbial growth from sample collections off the coast of Oregon and 576 attempts from groundwater at McClellan Air Force Base (MAFB). However, using the HTC approach up to 14% of the microorganisms counted by direct microscopy were cultured. In contrast, less than 1% of the microorganisms from natural environments that are observed under a microscope can be grown using standard agar plating techniques. This newly developed technique was successful at bringing into culture 11 previously uncultured or undescribed Proteobacteria. Four were isolated from the marine environment including, members of the SAR11 clade (alpha subclass), OM43 (beta-subclass), SAR92 (gamma subclass), and OM60/OM241 (gamma subclass). SARI 1 was transiently cultured in this study but was later successfully brought into culture using these HTC techniques by Mike Rappé. Eight were isolated from a trichloroethene (TCE) and cis-dichloroethene (cis-DCE) contaminated aquifer, including members of the MHP14 clade (alpha subclass), 4-Org1-14 clade (alpha subclass), Herbaspirillum/Oxalobacter clade (beta subclass), HTCC333 (beta subclass), HTCC410 (beta subclass), PM1 clade (beta subclass), Boom-7m-04 clade (beta subclass) and OM43 clade (beta subclass). Culturing microorganisms is an important step towards understanding their physiology and ecology, and in most cases is necessary for the formal systematic description of a new species. For microorganisms of global significance, such as the major uncultured bacterioplankton and soil microbiota, obtaining cultures is a prerequisite for obtaining complete genome sequences and understanding the relevance of these microorganisms to biogeochemical cycles.
机译:在过去的十年中,对自然环境的研究充满了使用与文化无关的方法进行的微生物多样性研究。 16S rRNA基因的克隆和测序一直是扩大人们对以前未发现的微生物多样性的认识的驱动力。众所周知的未经培养的微生物种类很多,并且已知的细菌系统发生分裂的一半在任何培养物中均不存在。不再假定从环境中获得的培养物代表了该环境中的优势或重要的生物。为了将这些广泛的和未培养的微生物中的一些引入培养中,开发了高通量培养(HTC)技术。在3年的时间里,从俄勒冈州沿海样本收集的微生物中筛选了2484次培养尝试,从麦克莱伦空军基地(MAFB)的地下水中筛选了576种尝试。但是,使用HTC方法,最多可培养14%通过直接显微镜检查计数的微生物。相反,在显微镜下观察到的来自自然环境的微生物中,只有不到1%的微生物可以使用标准的琼脂平板培养技术进行培养。这项新开发的技术成功地将11种先前未培养或未描述过的变形杆菌引入培养物中。从海洋环境中分离出了四个,包括SAR11进化枝(alpha子类),OM43(beta子类),SAR92(γ子类)和OM60 / OM241(γ子类)。 SARI 1在此研究中进行了瞬时培养,但后来由MikeRappé使用这些HTC技术成功地将其用于培养。从受三氯乙烯(TCE)和被顺二氯乙烯( cis -DCE)污染的含水层中分离出八种,包括MHP14进化枝(alpha子类),4-Org1-14进化枝(alpha子类), 草药螺旋杆菌/草酸杆菌(italia)进化枝(beta子类别),HTCC333(beta子类别),HTCC410(beta子类别),PM1进化枝(beta子类别),Boom-7m-04进化枝(beta子类别)和OM43进化枝(beta子类)。培养微生物是迈向了解其生理学和生态学的重要一步,而且在大多数情况下,对新物种进行正式的系统描述是必需的。对于具有全球意义的微生物,例如主要的未培养浮游细菌和土壤微生物,获得培养物是获得完整基因组序列和了解这些微生物与生物地球化学循环的相关性的前提。

著录项

  • 作者

    Connon, Stephanie Ann.;

  • 作者单位

    Oregon State University.;

  • 授予单位 Oregon State University.;
  • 学科 Biology Microbiology.; Environmental Sciences.; Biology Oceanography.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 149 p.
  • 总页数 149
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 微生物学;环境科学基础理论;海洋生物;
  • 关键词

  • 入库时间 2022-08-17 11:44:38

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