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通过链霉素抗性叠加培育高产达托霉素菌株。

Breeding of High Daptomycin-Producing Strain by Streptomycin Resistance Superposition.

机构信息

College of Life Science and Agricultural Engineering, Nanyang Normal University, Nanyang, China.

Research Center of Henan Provincial Agricultural Biomass Resource Engineering and Technology, Nanyang, China.

出版信息

Pol J Microbiol. 2022 Sep 24;71(3):463-471. doi: 10.33073/pjm-2022-041. eCollection 2022 Sep 1.

DOI:10.33073/pjm-2022-041
PMID:36185027
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9608166/
Abstract

Daptomycin is a cyclolipopeptide antibiotic produced by . It is widely used to treat drug-resistant bacterial infections; however, daptomycin yield in wild strains is very low. To improve the daptomycin production by the strain BNCC 342432, a modified method of ribosome engineering with superposition of streptomycin resistance was adopted in this study. The highest-yield mutant strain SR-2620 was obtained by increasing streptomycin resistance of BNCC 342432, and achieved daptomycin production of 38.5 mg/l in shake-flask fermentation, 1.79-fold higher than the parent strain and its heredity stability was stable. The morphological characteristics of the two strains were significantly different, and the 440 base G of the gene in the mutant strain was deleted, which resulted in a frameshift mutation. Our results demonstrate that gradually increasing strain resistance to streptomycin was an effective breeding method to improve daptomycin yield in .

摘要

达托霉素是一种由 产生的环脂肽抗生素。它被广泛用于治疗耐药菌感染;然而,野生菌株中的达托霉素产量非常低。为了提高 BNCC 342432 菌株的达托霉素产量,本研究采用核糖体工程与链霉素抗性叠加的改良方法。通过提高 BNCC 342432 的链霉素抗性,获得了最高产突变株 SR-2620,在摇瓶发酵中达托霉素产量达到 38.5mg/L,比亲本菌株提高了 1.79 倍,遗传稳定性稳定。两株菌的形态特征有明显差异,突变株中 基因的 440 个碱基 G 缺失,导致移码突变。我们的结果表明,逐渐提高菌株对链霉素的抗性是提高 的达托霉素产量的有效育种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/338a4a778636/pjm-71-463-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/5bb040c3c6ea/pjm-71-463-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/babe2fce9814/pjm-71-463-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/6040d5f67760/pjm-71-463-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/ebc230142ba6/pjm-71-463-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/6dac396748eb/pjm-71-463-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/338a4a778636/pjm-71-463-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/5bb040c3c6ea/pjm-71-463-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/babe2fce9814/pjm-71-463-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/6040d5f67760/pjm-71-463-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/ebc230142ba6/pjm-71-463-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/6dac396748eb/pjm-71-463-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6a/9608166/338a4a778636/pjm-71-463-g005.jpg

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