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大肠杆菌K1中多聚唾液酸荚膜的生物合成与组装。低密度囊泡组分在唾液酸聚合物内源性合成激活中的作用。

Biosynthesis and assembly of the polysialic acid capsule in Escherichia coli K1. Role of a low-density vesicle fraction in activation of the endogenous synthesis of sialyl polymers.

作者信息

Whitfield C, Adams D A, Troy F A

出版信息

J Biol Chem. 1984 Oct 25;259(20):12769-75.

PMID:6386802
Abstract

Escherichia coli K1 synthesizes a polysialic acid capsule when grown at 37 but not 15 degrees C. The derangement in sialyl polymer synthesis appears to result from the inability of 15 degrees C membranes to synthesize or assemble a functional endogenous acceptor (Troy, F.A., and McCloskey, M.A. (1979) J. Biol. Chem. 254, 7377-7387). Membranes from cells grown at 15 degrees C spontaneously gained the ability to synthesize sialyl polymer after incubation at 33 degrees C for 2-4 h. The incubation-dependent activation of the endogenous synthesis of sialyl polymer in 15 degrees C membranes possessed two unusual features. First, the sialyltransferase was localized in a low density vesicle fraction (LDV; rho = 1.11 g/cm3). Second, this fraction catalyzed protein synthesis, and protein synthesis was required for activation. A study of the LDV fraction showed: 1) their light density resulted from a 5- to 8-fold enrichment in lipid phosphate to protein ratio and their sialyltransferase activity was enriched 40-fold compared with unfractionated total membranes; 2) they contained proteins characteristic of inner and outer membranes including leader peptidase and lipoprotein; 3) they constituted 8% of the mass of unfractionated total membranes yet contained all of the endogenous sialyltransferase activity in 15 degrees C membranes. In contrast, LDV from 37 degrees C grown cells accounted for 4.8% of the membrane mass and only 12.5% of the endogenous sialyltransferase activity; 4) they were multilamellar and averaged 0.7 mu in diameter. Based on these results, we believe the LDV fraction is of physiological importance in sialyl polymer synthesis. Growth at 15 degrees C allowed identification and study of the LDV fraction possibly because of the altered thermotropic properties of the membrane phospholipids that occur when E. coli is grown at low temperature.

摘要

大肠杆菌K1在37℃生长时会合成多聚唾液酸荚膜,但在15℃时则不会。唾液酸聚合物合成的紊乱似乎是由于15℃的细胞膜无法合成或组装功能性内源性受体(Troy, F.A., and McCloskey, M.A. (1979) J. Biol. Chem. 254, 7377 - 7387)。来自在15℃生长的细胞的膜在33℃孵育2 - 4小时后自发获得了合成唾液酸聚合物的能力。15℃膜中唾液酸聚合物内源性合成的孵育依赖性激活具有两个不寻常的特征。首先,唾液酸转移酶定位于低密度囊泡部分(LDV;ρ = 1.11 g/cm³)。其次,该部分催化蛋白质合成,并且激活需要蛋白质合成。对LDV部分的研究表明:1)它们的低密度是由于脂质磷酸与蛋白质的比例富集了5至8倍,并且它们的唾液酸转移酶活性与未分级的总膜相比富集了40倍;2)它们含有内膜和外膜特有的蛋白质,包括前导肽酶和脂蛋白;3)它们占未分级总膜质量的8%,但包含15℃膜中所有的内源性唾液酸转移酶活性。相比之下,来自在37℃生长的细胞的LDV占膜质量的4.8%,仅占内源性唾液酸转移酶活性的12.5%;4)它们是多层的,平均直径为0.7微米。基于这些结果,我们认为LDV部分在唾液酸聚合物合成中具有生理重要性。在15℃生长使得能够鉴定和研究LDV部分,这可能是因为当大肠杆菌在低温下生长时膜磷脂的热致性质发生了改变。

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