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河口沉积物中胞外聚合物的保存

Preservation of exopolymeric substances in estuarine sediments.

作者信息

Duteil Thibault, Bourillot Raphaël, Braissant Olivier, Grégoire Brian, Leloup Maud, Portier Eric, Brigaud Benjamin, Féniès Hugues, Svahn Isabelle, Henry Adrien, Yokoyama Yusuke, Visscher Pieter T

机构信息

Univ. Bordeaux, CNRS, Bordeaux INP, EPOC, UMR 5805, Pessac, France.

Department Biomedical Engineering (DBE), Center for Biomechanics and Biocalorimetry, University of Basel, Allschwil, Switzerland.

出版信息

Front Microbiol. 2022 Aug 18;13:921154. doi: 10.3389/fmicb.2022.921154. eCollection 2022.

DOI:10.3389/fmicb.2022.921154
PMID:36060749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9434125/
Abstract

The surface of intertidal estuarine sediments is covered with diatom biofilms excreting exopolymeric substances (EPSs) through photosynthesis. These EPSs are highly reactive and increase sediment cohesiveness notably through organo-mineral interactions. In most sedimentary environments, EPSs are partly to fully degraded by heterotrophic bacteria in the uppermost millimeters of the sediment and so they are thought to be virtually absent deeper in the sedimentary column. Here, we present the first evidence of the preservation of EPSs and EPS-mineral aggregates in a 6-m-long sedimentary core obtained from an estuarine point bar in the Gironde Estuary. EPSs were extracted from 18 depth intervals along the core, and their physicochemical properties were characterized by (i) wet chemical assays to measure the concentrations of polysaccharides and proteins, and EPS deprotonation of functional groups, (ii) acid-base titrations, and (iii) Fourier transform infrared spectroscopy. EPS-sediment complexes were also imaged using cryo-scanning electron microscopy. EPS results were analyzed in the context of sediment properties including facies, grain size, and total organic carbon, and of metabolic and enzymatic activities. Our results showed a predictable decrease in EPS concentrations (proteins and polysaccharides) and reactivity from the surface biofilm to a depth of 0.5 m, possibly linked to heterotrophic degradation. Concentrations remained relatively low down to 4.3 m deep. Surprisingly, at that depth EPSs abundance was comparable to the surface and showed a downward decrease to 6.08 m. cryo-scanning electron microscopy (Cryo-SEM) showed that the EPS complexes with sediment were abundant at all studied depth and potentially protected EPSs from degradation. EPS composition did not change substantially from the surface to the bottom of the core. EPS concentrations and acidity were anti-correlated with metabolic activity, but showed no statistical correlation with grain size, TOC, depth or enzymatic activity. Maximum EPS concentrations were found at the top of tide-dominated sedimentary sequences, and very low concentrations were found in river flood-dominated sedimentary sequences. Based on this observation, we propose a scenario where biofilm development and EPS production are maximal when (i) the point bar and the intertidal areas were the most extensive, i.e., tide-dominated sequences and (ii) the tide-dominated deposit were succeeded by rapid burial beneath sediments, potentially decreasing the probability of encounter between bacterial cells and EPSs.

摘要

潮间带河口沉积物表面覆盖着硅藻生物膜,这些生物膜通过光合作用分泌胞外聚合物(EPSs)。这些EPSs具有高反应活性,并通过有机-矿物相互作用显著增强沉积物的黏性。在大多数沉积环境中,EPSs在沉积物最上层几毫米内会被异养细菌部分或完全降解,因此人们认为在沉积柱更深的地方实际上不存在EPSs。在此,我们首次展示了在从吉伦特河口一个河口沙坝获取的6米长沉积岩芯中保存有EPSs和EPS-矿物聚集体的证据。沿着岩芯从18个深度间隔提取了EPSs,并通过以下方法对其物理化学性质进行了表征:(i)湿化学分析,以测量多糖和蛋白质的浓度以及EPS官能团的去质子化情况;(ii)酸碱滴定;(iii)傅里叶变换红外光谱。还使用低温扫描电子显微镜对EPS-沉积物复合体进行了成像。结合沉积物性质(包括岩相、粒度和总有机碳)以及代谢和酶活性对EPS结果进行了分析。我们的结果表明,从表面生物膜到0.5米深度,EPS浓度(蛋白质和多糖)及反应活性呈现可预测的下降,这可能与异养降解有关。在4.3米深处之前,浓度一直相对较低。令人惊讶的是,在该深度EPSs丰度与表面相当,并呈现向下递减直至6.08米。低温扫描电子显微镜(Cryo-SEM)显示,在所有研究深度,EPS与沉积物的复合体都很丰富,并且可能保护了EPSs不被降解。从岩芯表面到底部,EPS组成没有实质性变化。EPS浓度和酸度与代谢活性呈负相关,但与粒度、总有机碳、深度或酶活性无统计学相关性。在潮汐主导的沉积层序顶部发现了最高的EPS浓度,而在河流洪水主导的沉积层序中发现了非常低的浓度。基于这一观察结果,我们提出了一种情形:当(i)沙坝和潮间带区域最为广阔,即潮汐主导的层序,以及(ii)潮汐主导的沉积物之后被沉积物快速掩埋时,生物膜发育和EPS产生达到最大,这可能降低了细菌细胞与EPSs相遇的概率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/1810a81c1499/fmicb-13-921154-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/b703580bd602/fmicb-13-921154-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/7c10346775e4/fmicb-13-921154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/26641eae1190/fmicb-13-921154-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/2312289f05f9/fmicb-13-921154-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/a549c75a8005/fmicb-13-921154-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/df4b1f2fcf46/fmicb-13-921154-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/1810a81c1499/fmicb-13-921154-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/b703580bd602/fmicb-13-921154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/5a2c0d6b84e2/fmicb-13-921154-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/7c10346775e4/fmicb-13-921154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/26641eae1190/fmicb-13-921154-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/2312289f05f9/fmicb-13-921154-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/a549c75a8005/fmicb-13-921154-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/df4b1f2fcf46/fmicb-13-921154-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6948/9434125/1810a81c1499/fmicb-13-921154-g008.jpg

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