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同位素示踪表明,少数海洋黄杆菌和γ-变形菌能够单个细胞地同化大型海藻多糖。

Isotopic tracing reveals single-cell assimilation of a macroalgal polysaccharide by a few marine Flavobacteria and Gammaproteobacteria.

机构信息

Sorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M), Station Biologique de Roscoff (SBR), Roscoff, France.

Institut Curie, Université Paris-Saclay, Paris, France.

出版信息

ISME J. 2021 Oct;15(10):3062-3075. doi: 10.1038/s41396-021-00987-x. Epub 2021 May 5.

DOI:10.1038/s41396-021-00987-x
PMID:33953365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8443679/
Abstract

Algal polysaccharides constitute a diverse and abundant reservoir of organic matter for marine heterotrophic bacteria, central to the oceanic carbon cycle. We investigated the uptake of alginate, a major brown macroalgal polysaccharide, by microbial communities from kelp-dominated coastal habitats. Congruent with cell growth and rapid substrate utilization, alginate amendments induced a decrease in bacterial diversity and a marked compositional shift towards copiotrophic bacteria. We traced C derived from alginate into specific bacterial incorporators and quantified the uptake activity at the single-cell level, using halogen in situ hybridization coupled to nanoscale secondary ion mass spectrometry (HISH-SIMS) and DNA stable isotope probing (DNA-SIP). Cell-specific alginate uptake was observed for Gammaproteobacteria and Flavobacteriales, with carbon assimilation rates ranging from 0.14 to 27.50 fg C µm h. DNA-SIP revealed that only a few initially rare Flavobacteriaceae and Alteromonadales taxa incorporated C from alginate into their biomass, accounting for most of the carbon assimilation based on bulk isotopic measurements. Functional screening of metagenomic libraries gave insights into the genes of alginolytic Alteromonadales active in situ. These results highlight the high degree of niche specialization in heterotrophic communities and help constraining the quantitative role of polysaccharide-degrading bacteria in coastal ecosystems.

摘要

海藻多糖构成了海洋异养细菌有机物质的一个多样化和丰富的储存库,是海洋碳循环的核心。我们研究了来自海带占主导地位的沿海生境的微生物群落对褐藻胶(一种主要的大型海藻多糖)的吸收。与细胞生长和快速底物利用一致,褐藻酸盐的添加导致细菌多样性降低,并且朝着富营养细菌的明显组成变化。我们通过卤化物原位杂交与纳米二次离子质谱(HISH-SIMS)和 DNA 稳定同位素探测(DNA-SIP)将源自褐藻酸盐的 C 追踪到特定的细菌掺入者,并在单细胞水平上定量了吸收活性。观察到 Gammaproteobacteria 和 Flavobacteriales 对细胞特异性褐藻酸盐的摄取,碳同化率范围为 0.14 到 27.50 fg C µm h。DNA-SIP 表明,只有少数最初罕见的黄杆菌科和交替单胞菌门类群将 C 从褐藻酸盐中同化到其生物量中,根据总同位素测量,这占了大部分碳同化。对宏基因组文库的功能筛选提供了对原位活性的具有藻酸酶的交替单胞菌门基因的深入了解。这些结果突出了异养群落中高度的生态位特化,并有助于限制多糖降解细菌在沿海生态系统中的定量作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/979097ec507d/41396_2021_987_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/83a1b699f016/41396_2021_987_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/a1e4f28eb721/41396_2021_987_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/a1d75f16cbf8/41396_2021_987_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/f98a6f351862/41396_2021_987_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/8f7fd3020a7a/41396_2021_987_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/979097ec507d/41396_2021_987_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/83a1b699f016/41396_2021_987_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/a1e4f28eb721/41396_2021_987_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/a1d75f16cbf8/41396_2021_987_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/f98a6f351862/41396_2021_987_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/8f7fd3020a7a/41396_2021_987_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e613/8443679/979097ec507d/41396_2021_987_Fig6_HTML.jpg

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