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硫化物诱导湖沼颤藻中一种周质蛋白的合成

Sulfide induction of synthesis of a periplasmic protein in the cyanobacterium Oscillatoria limnetica.

作者信息

Arieli B, Binder B, Shahak Y, Padan E

机构信息

Division of Microbial and Molecular Ecology, Hebrew University of Jerusalem, Israel.

出版信息

J Bacteriol. 1989 Feb;171(2):699-702. doi: 10.1128/jb.171.2.699-702.1989.

Abstract

Two proteins which may play a role in the induction of anoxygenic photosynthesis in Oscillatoria limnetica have been demonstrated by comparing the pattern of labeling during pulses of [35S]methionine of cells incubated under inducing conditions [anaerobic conditions plus 3-(3,4-dichlorophenyl)-1,1-dimethylurea, light, and sulfide) with that of cells incubated under noninducing conditions (without sulfide). The major inducible protein has an apparent molecular mass of 11.5 kilodaltons and is associated with a less strongly labeled 12.5-kilodalton protein. The synthesis of both proteins commences within the first 30 min of induction and continues throughout the 2-h induction period. Since these proteins are not synthesized in the presence of dithionite without sulfide, low redox potential alone is insufficient as an inducer of these proteins. Lysozyme treatment and/or osmotic shock of intact cells results in the release of the sulfide-induced proteins. Our data thus indicate that these proteins are located in the periplasmic space of the cells.

摘要

通过比较在诱导条件下(厌氧条件加3-(3,4-二氯苯基)-1,1-二甲基脲、光照和硫化物)培养的细胞与在非诱导条件下(无硫化物)培养的细胞在[35S]甲硫氨酸脉冲期间的标记模式,已证明两种可能在湖沼颤藻中诱导无氧光合作用中起作用的蛋白质。主要的可诱导蛋白表观分子量为11.5千道尔顿,并且与一种标记较弱的12.5千道尔顿蛋白相关。两种蛋白质的合成在诱导的最初30分钟内开始,并在整个2小时的诱导期内持续。由于这些蛋白质在无硫化物的连二亚硫酸盐存在下不合成,仅低氧化还原电位不足以作为这些蛋白质的诱导剂。完整细胞的溶菌酶处理和/或渗透压休克导致硫化物诱导的蛋白质释放。因此,我们的数据表明这些蛋白质位于细胞的周质空间中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d018/209653/462994ab0aeb/jbacter00168-0090-a.jpg

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