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CsgA, an extracellular protein essential for Myxococcus xanthus development.

作者信息

Shimkets L J, Rafiee H

机构信息

Department of Microbiology, University of Georgia, Athens 30602.

出版信息

J Bacteriol. 1990 Sep;172(9):5299-306. doi: 10.1128/jb.172.9.5299-5306.1990.

DOI:10.1128/jb.172.9.5299-5306.1990
PMID:2118510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC213193/
Abstract

CsgA mutants of Myxococcus xanthus appear to be defective in producing an extracellular molecule essential for the developmental behaviors of this bacterium. The csgA gene encodes a 17.7-kilodalton polypeptide whose function and cellular location were investigated with immunological probes. Large quantities of the CsgA gene product were obtained from a lacZ-csgA translational gene fusion expressed in Escherichia coli. The chimeric 21-kilodalton protein was purified by preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Affinity-purified polyclonal antibodies raised against the fusion protein were used to determine the cellular location of the native CsgA protein by colloidal gold labeling and transmission electron microscopy. Between 1,100 and 2,200 extracellular molecules of CsgA per developing M. xanthus cell were detected, most of which were associated with the extracellular matrix. The anti-CsgA antibodies inhibited wild-type development unless they were first neutralized with the fusion protein. Together these results suggest that the CsgA gene product has an essential, extracellular function during development, possibly as a pheromone.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/5216fe6f1a91/jbacter00123-0575-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/38ec0daa5717/jbacter00123-0571-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/a209bd03abb6/jbacter00123-0571-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/2ae1a60ae1f1/jbacter00123-0572-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/81ccd72b88ec/jbacter00123-0573-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/a5d2030e17f6/jbacter00123-0574-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/5216fe6f1a91/jbacter00123-0575-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/38ec0daa5717/jbacter00123-0571-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/a209bd03abb6/jbacter00123-0571-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/2ae1a60ae1f1/jbacter00123-0572-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/81ccd72b88ec/jbacter00123-0573-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/a5d2030e17f6/jbacter00123-0574-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629f/213193/5216fe6f1a91/jbacter00123-0575-a.jpg

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CsgA, an extracellular protein essential for Myxococcus xanthus development.
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本文引用的文献

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Developmental cell interactions in Myxococcus xanthus and the spoC locus.粘细菌 Myxococcus xanthus 中的发育细胞相互作用和 spoC 基因座。
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Cell-to-cell stimulation of movement in nonmotile mutants of Myxococcus.粘球菌非运动突变体中细胞间运动刺激
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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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Perchlorate-Reducing Bacteria from Hypersaline Soils of the Colombian Caribbean.来自哥伦比亚加勒比地区高盐土壤的高氯酸盐还原菌
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Deletion of genes involved in the ketogluconate metabolism, Entner-Doudoroff pathway, and glucose dehydrogenase increase local and invasive virulence phenotypes in Streptococcus pneumoniae.酮葡糖酸盐代谢、恩特纳-道多罗夫途径和葡萄糖脱氢酶相关基因缺失增强肺炎链球菌的局部和侵袭性毒力表型。
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