赖氨酸生产菌株短杆菌IMV B-7447的化学诱变

G. Andriiash
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引用次数: 0

摘要

这项工作的目的是使用化学诱变方法获得赖氨酸积累增加的生产菌株。方法。为了实现这一目标,我们使用化学诱变剂N-甲基-N-硝基-N-亚硝基胍处理赖氨酸产生菌株,培养得到的克隆,并在烧瓶和生物反应器中测定赖氨酸的积累。后果找到了产生突变微生物的诱变剂作用的最佳浓度和持续时间。选择赖氨酸积累量最大的菌株。连续进行三次诱变。结果,获得了赖氨酸产生菌株短杆菌IMV B-7796,其关于亮氨酸和苏氨酸的营养缺陷型,具有目标氨基酸的最大积累。结论。获得赖氨酸生产商短杆菌IMV B-7796,其在生物反应器中在定期培养和饲养的条件下生产65.0g/dm3的赖氨酸。短杆菌IMV B-7796菌株被提议作为创建赖氨酸积累增加的转基因菌株的基础,以进一步用于工业赖氨酸技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CHEMICAL MUTAGENESIS OF THE LYSINE-PRODUCING STRAIN Brevibacterium sp. IMV B-7447
The aim of the work was to obtain a producer strain with increased lysine accumulation using the chemical mutagenesis method. Methods. To achieve the goal, we used the method of treating the lysine-producing strain with the chemical mutagen N-methyl-N-nitro-N-nitrosoguanidine, cultivating the resulting clone and determining the accumulation of lysine in flasks and a bioreactor. Results. The optimal concentrations and duration of mutagen action for the production of mutant microorganisms were found. Сlones with the maximum lysine accumulation were selected. Mutagenesis was carried out consecutively three times. As a result, lysine-producing strain Brevibacterium sp. IMV B-7796 auxotrophic regarding leucine and threonine with maximum accumulation of the target amino acid was obtained. Conclusions. The lysine producer Brevibacterium sp. IMV B-7796 was obtained, which produced 65.0 g/dm3 of lysine in a bioreactor under conditions of periodic cultivation with feeding. The Brevibacterium sp. IMV B-7796 strain was proposed as a basis for the creation of a genetically modified strain with increased accumulation of lysine for further use in industrial lysine technology.
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