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解脲脲原体中磷脂酶A和C内源性活性的定位

Localization of endogenous activity of phospholipases A and C in Ureaplasma urealyticum.

作者信息

De Silva N S, Quinn P A

机构信息

Department of Microbiology, Hospital for Sick Children, Toronto, Canada.

出版信息

J Clin Microbiol. 1991 Jul;29(7):1498-503. doi: 10.1128/jcm.29.7.1498-1503.1991.

DOI:10.1128/jcm.29.7.1498-1503.1991
PMID:1885745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC270141/
Abstract

Endogenous activities of phospholipases A and C in Ureaplasma urealyticum were assayed in cellular fractions of exponential-phase cells. Enzymatic studies indicated that ATPase activity was localized in the plasma membrane fraction and NADH and NADPH dehydrogenase activities were localized in the cytosol fraction. Studies with purified ureaplasma membranes demonstrated that, of three serovars tested, endogenous phospholipase A1, A2, and C activities were localized in the plasma membrane. Very low levels of activity were observed in the cytosol fractions. Phospholipase A2 activity in the plasma membrane was 3- to 5-fold higher than the activity in the lysates and 60- to 300-fold higher than the activity of phospholipase A1. Phospholipase C was localized mainly in the plasma membrane, with 20% found in the cytosol fraction. The levels of activity were comparable among the three serovars. There was a significantly lower level of activity in cells from the stationary growth phase than in the exponential phase. Significant differences were observed in the phospholipase A activities among the U. urealyticum serovars 3, 4, and 8. Phospholipase A2 activity was twofold higher in serovar 8 membranes, and phospholipase A1 activity was twofold higher in serovar 3 membranes. These results demonstrate that endogenous activities of phospholipase A and C are localized primarily in the plasma membrane fraction of U. urealyticum. The specific activities in the membranes of the phospholipases varied among the three serovars. Phospholipase enzymes may function as virulence factors in U. urealyticum and may vary among the serovars.

摘要

对解脲脲原体指数生长期细胞的细胞组分中磷脂酶A和C的内源性活性进行了测定。酶学研究表明,ATP酶活性定位于质膜组分,而NADH和NADPH脱氢酶活性定位于胞质溶胶组分。对纯化的脲原体膜进行的研究表明,在所测试的3个血清型中,内源性磷脂酶A1、A2和C活性定位于质膜。在胞质溶胶组分中观察到的活性水平非常低。质膜中的磷脂酶A2活性比裂解物中的活性高3至5倍,比磷脂酶A1的活性高60至300倍。磷脂酶C主要定位于质膜,20%存在于胞质溶胶组分中。3个血清型的活性水平相当。稳定生长期细胞中的活性水平明显低于指数生长期。在解脲脲原体血清型3、4和8之间观察到磷脂酶A活性存在显著差异。血清型8膜中的磷脂酶A2活性高两倍,血清型3膜中的磷脂酶A1活性高两倍。这些结果表明,磷脂酶A和C的内源性活性主要定位于解脲脲原体的质膜组分。3个血清型中磷脂酶在膜中的比活性各不相同。磷脂酶可能在解脲脲原体中作为毒力因子起作用,并且在不同血清型之间可能有所不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c2e/270141/ae20eed84986/jcm00043-0236-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c2e/270141/ae20eed84986/jcm00043-0236-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c2e/270141/ae20eed84986/jcm00043-0236-a.jpg

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