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一种使用双重包囊技术原位培养微生物的方法。

An in situ method for cultivating microorganisms using a double encapsulation technique.

作者信息

Ben-Dov Eitan, Kramarsky-Winter Esti, Kushmaro Ariel

机构信息

Department of Biotechnology Engineering, Ben-Gurion University of the Negev, Be'er-Sheva, Israel.

出版信息

FEMS Microbiol Ecol. 2009 Jun;68(3):363-71. doi: 10.1111/j.1574-6941.2009.00682.x. Epub 2009 Apr 21.

Abstract

The lack of cultured microorganisms represents a bottleneck for advancement in microbiology. The development of novel culturing techniques is, therefore, a crucial step in our understanding of microbial diversity in general, and the role of such diversity in the environment, in particular. This study presents an innovative method for cultivating microorganisms by encapsulating them within agar spheres, which are then encased in a polysulfonic polymeric membrane and incubated in a simulated or natural environment. This method stimulates growth of the entrapped microorganisms by allowing them access to essential nutrients and cues from the environment. It allows for the discovery of microorganisms from dilutions that are 10-100-fold greater than possible with conventional plating techniques. Analysis of microorganisms grown in such spheres incubated in and on a number of different substrates yielded numerous novel ribotypes. For example, spheres incubated on the mucus surface of a Fungiid coral yielded numerous ribotypes, with only 50% sharing similarity (85-96%) to previously identified microorganisms. This suggests that many of the species represent novel ribotypes. Hence, the technique reported here advances our ability to retrieve and successfully culture microorganisms and provides an innovative tool to access unknown microbial diversity.

摘要

缺乏可培养的微生物是微生物学发展的一个瓶颈。因此,开发新的培养技术是我们全面了解微生物多样性,特别是这种多样性在环境中所起作用的关键一步。本研究提出了一种通过将微生物封装在琼脂球内来培养微生物的创新方法,然后将琼脂球包裹在聚磺酸聚合物膜中,并在模拟或自然环境中进行培养。这种方法通过使被捕获的微生物能够获取基本营养物质和来自环境的信号来刺激其生长。它能够从比传统平板培养技术所能检测到的浓度低10至100倍的稀释液中发现微生物。对在多种不同底物上及内部培养的琼脂球中生长的微生物进行分析,产生了许多新的核糖型。例如,在鹿角珊瑚的黏液表面培养的琼脂球产生了许多核糖型,其中只有50%与先前鉴定的微生物具有相似性(85 - 96%)。这表明许多物种代表了新的核糖型。因此,本文报道的技术提高了我们检索和成功培养微生物的能力,并提供了一种获取未知微生物多样性的创新工具。

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