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舒伊尔基尔假单胞菌原生质球破碎物对蛋白质和核酸的合成

Synthesis of protein and nucleic acid by disrupted spheroplasts of Pseudomonas schuylkilliensis.

作者信息

Mizuno S, Matsuzawa H, Nagata Y, Shibuya I, Takahashi H, Maruo B

出版信息

J Bacteriol. 1971 Feb;105(2):538-52. doi: 10.1128/jb.105.2.538-552.1971.

Abstract

Osmotically shocked spheroplasts obtained from Pseudomonas schuylkilliensis strain P contained about 54, 32, 28, and 82% of the total cellular protein, ribonucleic acid (RNA), deoxyribonucleic acid (DNA), and phospholipid, respectively. This preparation was capable of incorporating (32)P-orthophosphate into RNA and DNA, (3)H-adenosine or (3)H-uridine into RNA, and (3)H-leucine or (14)C-phenylalanine into protein. These activities were not found in the cytoplasmic fraction which contained most of the glucose-6-phosphate dehydrogenase activity. The synthesis of RNA by intact and disrupted spheroplast preparations was sensitive to actinomycin D, chromomycin A(3), streptovaricin, rifampin, Lubrol W, Triton X-100, and sodium deoxycholate, whereas RNA synthesis by intact cells was insensitive to these agents. Ethylenediaminetetraacetic acid, porcine pancreatic lipase, the protoplast-bursting factor, high concentrations of salts, and washing the preparation inhibited the synthesis of RNA by disrupted spheroplasts but had little or no effect on intact spheroplasts. Most of the newly synthesized RNA made by disrupted spheroplasts had the characteristics of messenger RNA. The DNA present in this preparation functioned as a template for RNA synthesis; continued protein synthesis was dependent on concomitant RNA synthesis. An unusual feature of the preparation was the finding that the synthesis of macromolecules was completely dependent on oxidative phosphorylation.

摘要

从斯库伊利基假单胞菌菌株P获得的经渗透压休克处理的原生质球分别含有约54%、32%、28%和82%的细胞总蛋白、核糖核酸(RNA)、脱氧核糖核酸(DNA)和磷脂。该制剂能够将(32)P - 正磷酸盐掺入RNA和DNA中,将(3)H - 腺苷或(3)H - 尿苷掺入RNA中,以及将(3)H - 亮氨酸或(14)C - 苯丙氨酸掺入蛋白质中。在含有大部分葡萄糖 - 6 - 磷酸脱氢酶活性的细胞质部分中未发现这些活性。完整和破碎的原生质球制剂合成RNA对放线菌素D、色霉素A(3)、链黑菌素、利福平、月桂醇聚醚W、曲拉通X - 100和脱氧胆酸钠敏感,而完整细胞合成RNA对这些试剂不敏感。乙二胺四乙酸、猪胰脂肪酶、原生质球破裂因子、高浓度盐以及洗涤该制剂会抑制破碎原生质球合成RNA,但对完整原生质球几乎没有影响或没有影响。破碎原生质球新合成的大部分RNA具有信使RNA的特征。该制剂中存在的DNA作为RNA合成的模板;持续的蛋白质合成依赖于伴随的RNA合成。该制剂的一个不寻常特征是发现大分子的合成完全依赖于氧化磷酸化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca05/248418/5372bc8a1c95/jbacter00374-0109-a.jpg

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