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用于海洋细菌培养的微囊化及培养方法

Microencapsulation and incubation methodology for the cultivation of marine bacteria.

作者信息

Pope Emily, Cartmell Christopher, Haltli Bradley, Ahmadi Ali, Kerr Russell G

机构信息

Department of Biomedical Science, University of Prince Edward Island, Charlottetown, PE, Canada.

Department of Chemistry, University of Prince Edward Island, Charlottetown, PE, Canada.

出版信息

Front Microbiol. 2022 Aug 22;13:958660. doi: 10.3389/fmicb.2022.958660. eCollection 2022.

Abstract

Environmental microorganisms are important sources of biotechnology innovations; however, the discovery process is hampered by the inability to culture the overwhelming majority of microbes. To drive the discovery of new biotechnology products from previously unculturable microbes, several methods such as modification of media composition, incubation conditions, single-cell isolation, and incubation, have been employed to improve microbial recovery from environmental samples. To improve microbial recovery, we examined the effect of microencapsulation followed by incubation on the abundance, viability, and diversity of bacteria recovered from marine sediment. Bacteria from marine sediment samples were resuspended or encapsulated in agarose and half of each sample was directly plated on agar and the other half inserted into modified Slyde-A-Lyzer™ dialysis cassettes. The cassettes were incubated in their natural environment () for a week, after which they were retrieved, and the contents plated. Colony counts indicated that bacterial abundance increased during incubation and that cell density was significantly higher in cassettes containing non-encapsulated sediment bacteria. Assessment of viability indicated that a higher proportion of cells in encapsulated samples were viable at the end of the incubation period, suggesting that agarose encapsulation promoted higher cell viability during incubation. One hundred and 46 isolates were purified from the study (32-38 from each treatment) to assess the effect of the four treatments on cultivable bacterial diversity. In total, 58 operational taxonomic units (OTUs) were identified using a 99% 16S rRNA gene sequence identity threshold. The results indicated that encapsulation recovered greater bacterial diversity from the sediment than simple resuspension (41 vs. 31 OTUs, respectively). While the cultivable bacterial diversity decreased by 43%-48% after incubation, difficult-to-culture () and obligate marine () taxa were only recovered after incubation. These results suggest that agarose encapsulation coupled with incubation in commercially available, low-cost, diffusion chambers facilitates the cultivation and improved recovery of bacteria from marine sediments. This study provides another tool that microbiologists can use to access microbial dark matter for environmental, biotechnology bioprospecting.

摘要

环境微生物是生物技术创新的重要来源;然而,发现过程因绝大多数微生物无法培养而受阻。为了推动从以前无法培养的微生物中发现新的生物技术产品,人们采用了多种方法,如改变培养基成分、培养条件、单细胞分离和培养,以提高从环境样品中回收微生物的效率。为了提高微生物回收率,我们研究了微囊化后培养对从海洋沉积物中回收的细菌的丰度、活力和多样性的影响。将海洋沉积物样品中的细菌重悬或包封在琼脂糖中,每个样品的一半直接接种在琼脂平板上,另一半插入改良的Slyde-A-Lyzer™透析盒中。将透析盒在其自然环境中培养一周,之后取出并将其中的内容物接种平板。菌落计数表明,培养过程中细菌丰度增加,并且含有未包封沉积物细菌的透析盒中的细胞密度显著更高。活力评估表明,培养期结束时,包封样品中存活细胞的比例更高,这表明琼脂糖包封在培养过程中促进了更高的细胞活力。从该研究中纯化了146个分离株(每种处理32 - 38个),以评估这四种处理对可培养细菌多样性的影响。使用99%的16S rRNA基因序列同一性阈值,总共鉴定出58个操作分类单元(OTU)。结果表明,与简单重悬相比,包封从沉积物中回收了更多的细菌多样性(分别为41个和31个OTU)。虽然培养后可培养细菌多样性下降了43% - 48%,但难培养和专性海洋分类群仅在培养后才被回收。这些结果表明,琼脂糖包封结合在市售低成本扩散室中培养有助于从海洋沉积物中培养和提高细菌回收率。这项研究提供了另一种工具,微生物学家可以用来获取微生物暗物质,用于环境、生物技术生物勘探。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5a5/9441948/e4ed486f9cf0/fmicb-13-958660-g001.jpg

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