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用去污剂破坏细胞膜后大肠杆菌丝状体的收缩。

Contraction of filaments of Escherichia coli after disruption of cell membrane by detergent.

作者信息

Koch A L, Lane S L, Miller J A, Nickens D G

出版信息

J Bacteriol. 1987 May;169(5):1979-84. doi: 10.1128/jb.169.5.1979-1984.1987.

DOI:10.1128/jb.169.5.1979-1984.1987
PMID:3553152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC212065/
Abstract

The osmotic pressure within a living bacterium creates stresses in the peptidoglycan that stretch the sacculus. We measured the amount of stretch by monitoring the shrinkage of growing cells of Escherichia coli after removal of the osmotic pressure by disruption of the phospholipid membranes with sodium dodecyl sulfate. Because the rods of the wild type are so short, length changes of filaments of longer than 7 microns were measured on phase-contrast micrographs. The filaments were prepared by growing ftsA and ftsI strains under permissive conditions in rich medium and then shifting them to 42 degrees C for 40 to 180 min. During this time, the mutant cells became elongated but did not divide. The growing filaments were mounted on a glass surface that had been treated with poly-L-lysine or RNase. The filaments were photographed before being treated with sodium dodecyl sulfate. The filaments were rephotographed at the time when the first change in phase contrast was noted. Some filaments were also measured at 10-min time intervals from 0 to 60 min. The reduction in phase contrast signaled the leakage of solutes and the loss of turgor pressure. The average length of the filaments decreased 17%. If the circumference were stretched to the same degree, then the surface area in vivo would be 45% greater than in the relaxed state. For comparison, a fully cross-linked monolayer of E. coli peptidoglycan in its most compact conformation could stretch up to 300% in achieving the most extended conformation possible without splitting covalent bonds.

摘要

活细菌内的渗透压会在肽聚糖中产生应力,从而拉伸细胞壁。我们通过监测用十二烷基硫酸钠破坏磷脂膜以去除渗透压后大肠杆菌生长细胞的收缩情况,来测量拉伸量。由于野生型的杆状细胞非常短,因此在相差显微镜照片上测量了长度超过7微米的细丝的长度变化。细丝是通过在丰富培养基中于允许条件下培养ftsA和ftsI菌株,然后将它们转移到42摄氏度下40至180分钟来制备的。在此期间,突变细胞伸长但不分裂。将生长的细丝固定在经过聚-L-赖氨酸或核糖核酸酶处理的玻璃表面上。在用十二烷基硫酸钠处理之前对细丝进行拍照。在注意到相差的第一次变化时对细丝重新拍照。一些细丝还在0至60分钟内每隔10分钟进行测量。相差的降低表明溶质泄漏和膨压丧失。细丝的平均长度减少了17%。如果周长以相同程度拉伸,那么体内的表面积将比松弛状态大45%。作为比较,处于最紧密构象的大肠杆菌肽聚糖的完全交联单层在不分裂共价键的情况下,在达到可能的最伸展构象时可拉伸高达300%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca9/212065/d55ef52de287/jbacter00195-0208-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca9/212065/d55ef52de287/jbacter00195-0208-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eca9/212065/d55ef52de287/jbacter00195-0208-a.jpg

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