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海洋束毛藻聚集体中固氮酶的免疫化学定位:与 N2 固定潜能的关系。

Immunochemical localization of nitrogenase in marine trichodesmium aggregates: relationship to n(2) fixation potential.

机构信息

Institute of Marine Sciences, University of North Carolina at Chapel Hill, Morehead City, North Carolina 28557, and Departments of Biology and Microbiology, Montana State University, Bozeman, Montana 59717.

出版信息

Appl Environ Microbiol. 1989 Nov;55(11):2965-75. doi: 10.1128/aem.55.11.2965-2975.1989.

Abstract

Colonial aggregation among nonheterocystous filaments of the planktonic marine cyanobacterium Trichodesmium is known to enhance N(2) fixation, mediated by the O(2)-sensitive enzyme complex nitrogenase. Expression of nitrogenase appears linked to the formation of O(2)-depleted microzones within aggregated bacterium-associated colonies. While this implies a mechanism by which nonheterocystous N(2) fixation can take place in an oxygenated water column, both the location and regulation of the N(2)-fixing apparatus remain unknown. We used an antinitrogenase polyclonal antibody together with postsection immunocolloidal gold staining and transmission electron microscopy to show that (i) virtually all Trichodesmium cells within a colony possessed nitrogenase, (ii) nitrogenase showed no clear intracellular localization, and (iii) certain associated bacteria contained nitrogenase. Our findings emphasize the critical role coloniality plays in regulating nitrogenase expression in nature. We interpret the potential for a large share of Trichodesmium cells to fix N(2) as an opportunistic response to the dynamic nature of the sea state; during quiescent conditions, aggregation and consequent expression of nitrogenase can proceed rapidly.

摘要

浮游海洋蓝藻 Trichodesmium 中非异形胞丝状藻的群体聚集已知可以增强由氧敏感酶复合物固氮酶介导的 N(2)固定。固氮酶的表达似乎与聚集的细菌相关菌落内形成缺氧微区有关。虽然这暗示了非异形胞 N(2)固定可以在含氧水柱中发生的机制,但固氮装置的位置和调节仍然未知。我们使用抗固氮酶多克隆抗体以及切片后免疫胶体金染色和透射电子显微镜,表明:(i) 群体中几乎所有的 Trichodesmium 细胞都具有固氮酶,(ii) 固氮酶没有明显的细胞内定位,(iii) 某些相关细菌含有固氮酶。我们的发现强调了群体在调节自然中固氮酶表达方面的关键作用。我们将 Trichodesmium 细胞大量固定 N(2)的可能性解释为对海洋状态动态性质的机会性反应;在静止条件下,聚集和随后的固氮酶表达可以迅速进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/759c/203199/f5f1d63b53fa/aem00104-0236-a.jpg

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