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通过发酵过程生产核酸相关物质。33. 产氨短杆菌突变体积累肌苷。

Production of nucleic acid-related substances by fermentation processes. 33. Accumulation of inosine by a mutant of Brevibacterium ammoniagenes.

作者信息

Furuya A, Abe S, Kinoshita S

出版信息

Appl Microbiol. 1970 Aug;20(2):263-70. doi: 10.1128/am.20.2.263-270.1970.

Abstract

Inosine-producing cultures were found among mutants resistant to 6-mercaptoguanine (6MG) derived from a 5'-inosinic acid (IMP)-producing strain, KY 13102, of Brevibacterium ammoniagenes. Inosine-producing ability was very frequent among the mutants resistant to a low concentration (10 to 50 mug/ml) of 6MG. The accumulation of inosine by strain KY 13714 was stimulated by a low concentration of adenine (25 mg/liter) but was depressed by high levels of adenine. The accumulation by strain KY 13714 was not inhibited by manganese ion but instead was stimulated by its excess, in contrast to IMP accumulation by KY 13102. Addition of hypoxanthine at an early stage of cultivation accelerated inosine accumulation. Furthermore, on addition of hypoxanthine and of a surface-activating agent after 48 hr of cultivation, the simultaneous accumulation of IMP and inosine was observed. A 9.3-mg amount of inosine per ml accumulated after 4 days of cultivation at 30 C. The inosine-producing mutant did not differ from the IMP-producing strain either in 5' purine nucleotide degradation or in IMP formation from hypoxanthine. However, it was found to be completely devoid of purine nucleoside-degrading activity. The conversion of IMP accumulation to inosine can be explained by the lack of nucleosidedegrading activity. The relationship between deficiency of nucleoside-degrading activity and resistance to low levels of 6MG is discussed, and a new mechanism for 6MG resistance is presented.

摘要

在源自产氨短杆菌5'-肌苷酸(IMP)生产菌株KY 13102的对6-巯基鸟嘌呤(6MG)具有抗性的突变体中发现了产肌苷培养物。在对低浓度(10至50微克/毫升)6MG具有抗性的突变体中,产肌苷能力非常常见。菌株KY 13714积累肌苷的过程受到低浓度腺嘌呤(25毫克/升)的刺激,但受到高浓度腺嘌呤的抑制。与KY 13102积累IMP相反,菌株KY 13714的积累不受锰离子抑制,反而受到过量锰离子的刺激。在培养早期添加次黄嘌呤可加速肌苷积累。此外,在培养48小时后添加次黄嘌呤和表面活性剂,可观察到IMP和肌苷同时积累。在30℃培养4天后,每毫升积累了9.3毫克肌苷。产肌苷突变体在5'嘌呤核苷酸降解或由次黄嘌呤形成IMP方面与产IMP菌株没有差异。然而,发现其完全缺乏嘌呤核苷降解活性。IMP积累向肌苷的转化可以用核苷降解活性的缺乏来解释。讨论了核苷降解活性缺乏与对低水平6MG抗性之间的关系,并提出了一种新的6MG抗性机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ca/376913/c4ec1d4ec985/applmicro00106-0112-a.jpg

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