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[细胞分裂素不会显著改变培养的大肠杆菌B中DNA腺嘌呤残基的甲基化情况]

[Cytokinins do not noticeably change the methylation of adenine residues of DNA in cultured Escherichia coli B].

作者信息

Vaniushin B F, Aleksandrushkina N I, Ogarkova O A

出版信息

Biokhimiia. 1989 Oct;54(10):1666-72.

PMID:2690961
Abstract

6-Benzylaminopurine (6-BAP) (1 mg/ml) does not influence the growth of E. coli B cell cultures or the number of [8-14C] labeled N6-methyladenine (m6A) residues in the total DNA [(100.m6A/(A x m6A) = 1.7]. The growth of bacterial cells in the presence of adenine or cytokinins (6-BAP, kinetin, zeatin) (1 mg/ml) was unaccompanied by significant changes in the intracellular content of plasmid pBR 322. The mode of restriction by endonuclease Cfu I hydrolyzing the Gm6ATC site of plasmids pBR 322 from E. coli B cells grown in the presence of adenine or one of the above-mentioned cytokinins is identical. These plasmids also have identical restriction products Mbo I or Sau 3AI. Thus, the cytokinins under study do not markedly affect the methylation of adenine residues in total DNA of E. coli B cell cultures and the GATC sequence in plasmids pBR 322 isolated from these cells.

摘要

6-苄氨基嘌呤(6-BAP)(1毫克/毫升)不影响大肠杆菌B细胞培养物的生长,也不影响总DNA中[8-14C]标记的N6-甲基腺嘌呤(m6A)残基的数量[(100.m6A/(A×m6A)=1.7]。在腺嘌呤或细胞分裂素(6-BAP、激动素、玉米素)(1毫克/毫升)存在的情况下,细菌细胞的生长并未伴随着质粒pBR 322细胞内含量的显著变化。在腺嘌呤或上述细胞分裂素之一存在的情况下生长的大肠杆菌B细胞中,内切酶Cfu I水解质粒pBR 322的Gm6ATC位点的限制模式是相同的。这些质粒也有相同的限制产物Mbo I或Sau 3AI。因此,所研究的细胞分裂素不会显著影响大肠杆菌B细胞培养物总DNA中腺嘌呤残基的甲基化以及从这些细胞中分离出的质粒pBR 322中的GATC序列。

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