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蛋白质和核糖核酸在脱氧核糖核酸与大肠杆菌其他细胞成分结合中的作用。

Involvement of protein and ribonucleic acid in the association of deoxyribonucleic acid with other cell components of Escherichia coli.

作者信息

Porter B, Fraser D K

出版信息

J Bacteriol. 1968 Jul;96(1):98-104. doi: 10.1128/jb.96.1.98-104.1968.

Abstract

Cells of Escherichia coli were labeled with precursors of ribonucleic acid (RNA), deoxyribonucleic acid (DNA), and protein, lysed with detergent, and examined by starch-block electrophoresis and CsCl density gradient centrifugation. A large amount of the DNA was seen to remain at positions of low electrophoretic mobility and light density along with tryptophan and arginine-containing proteins and some RNA. Addition of labeled, phenol-extracted DNA to unlabeled cells prior to lysis and electrophoresis showed that only a small amount of the DNA became associated during or after lysis. Sonic treatment of a lysate removed most of the DNA to a position of electrophoretic mobility and density similar to that of free DNA, whereas pronase and ribonuclease released only a part of the DNA. We concluded that binding of DNA to cell membranes or other cell components occurs in the cell prior to lysis and involves protein and probably a specific type of RNA.

摘要

用核糖核酸(RNA)、脱氧核糖核酸(DNA)和蛋白质的前体标记大肠杆菌细胞,用去污剂裂解细胞,然后通过淀粉块电泳和CsCl密度梯度离心进行检测。结果发现,大量的DNA与色氨酸、含精氨酸的蛋白质以及一些RNA一起,保留在电泳迁移率低和密度轻的位置。在裂解和电泳之前,将标记的、经苯酚提取的DNA添加到未标记的细胞中,结果表明,只有少量的DNA在裂解过程中或裂解后发生了结合。对裂解物进行超声处理后,大部分DNA迁移到了与游离DNA相似的电泳迁移率和密度位置,而链霉蛋白酶和核糖核酸酶仅释放出一部分DNA。我们得出结论,DNA与细胞膜或其他细胞成分的结合发生在细胞裂解之前,且涉及蛋白质,可能还涉及一种特定类型的RNA。

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Lysis of Escherichia coli with a neutral detergent.用中性去污剂裂解大肠杆菌。
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本文引用的文献

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THE IN VITRO FORMATION OF A DNA-RIBOSOME COMPLEX.DNA-核糖体复合物的体外形成
Proc Natl Acad Sci U S A. 1964 Jul;52(1):140-8. doi: 10.1073/pnas.52.1.140.
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Effect of sonic oscillation upon "old" and "new" nucleic acids in Escherichia coli.
Biochim Biophys Acta. 1961 Oct 14;53:19-28. doi: 10.1016/0006-3002(61)90790-9.
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Isolation of the DNA of the E. coli chromosome in one piece.完整分离大肠杆菌染色体的DNA。
Proc Natl Acad Sci U S A. 1966 Apr;55(4):792-7. doi: 10.1073/pnas.55.4.792.

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