Modification of ε-poly-L-lysine in vivo to reduce self-toxicity and enhance antibiotic overproduction

被引:1
作者
Ding, Jin [1 ,2 ]
Liang, Hengyu [3 ,4 ]
Fu, Shuai [5 ]
Liu, Ran [1 ,2 ,5 ]
Deng, Zixin [1 ,2 ,4 ]
Liu, Tiangang [1 ,2 ,4 ]
机构
[1] Wuhan Univ, Minist Educ, Key Lab Combinatorial Biosynth & Drug Discovery, Wuhan 430071, Hubei, Peoples R China
[2] Wuhan Univ, Sch Pharmaceut Sci, Wuhan 430071, Hubei, Peoples R China
[3] Amtech Biotech Co Ltd, Heilongjiang Engn & Res Ctr Nat Food Preservat, Qiqihar 161031, Peoples R China
[4] Wuhan Inst Biotechnol, Hubei Engn Lab Synthet Microbiol, Wuhan 430075, Hubei, Peoples R China
[5] J1 Biotech Co Ltd, Wuhan 430075, Hubei, Peoples R China
关键词
Streptomyces albulus; epsilon-poly-L-lysine; 2-epsilon-poly(L-lys)-glycerol; antibiotic; small-molecule residue modification; STREPTOMYCES-ALBULUS; DEGRADING ENZYME; GENE-CLUSTER; BIOSYNTHESIS; BACTERIA; PURIFICATION; INHIBITION; POLYLYSINE; RESISTANCE; MECHANISM;
D O I
10.1002/aic.16190
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
epsilon-poly-L-lysine (epsilon-PL) is a novel commercial food preservative, and glucose and glycerol are two carbon sources commonly used in epsilon-PL fermentation. Using MALDI-TOF and NMR, when grown in glycerol-based medium, but not glucose-based medium is determined, Streptomyces albulus J1-005 produces a derivative of epsilon-PL in which the terminal carboxyl group is modified with the second hydroxyl group of glycerol. Interestingly, this derivative, 2-epsilon-poly(L-lys)-glycerol, was hydrolyzed back to epsilon-PL when the pH was adjusted from 3.7 to the neutral range. Antimicrobial assays indicated that, compared to epsilon-PL, 2-epsilon-poly(L-lys)-glycerol has similar inhibitory activity against several bacterial species but is less inhibitory to the producing strain. Additionally, in fed-batch fermentation, product yield was 37% higher in glycerol-based medium than in medium containing an equal amount of glucose. Hence, we propose that such culture-based approaches for modifying toxic compounds in vivo can be a promising strategy for antibiotic overproduction. (c) 2018 American Institute of Chemical Engineers
引用
收藏
页码:4187 / 4192
页数:6
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