Rational reformation of Corynebacterium glutamicum for producing L-lysine by one-step fermentation from raw corn starch

被引:5
|
作者
Li, Chang-Long [1 ]
Ruan, Hao-Zhe [1 ]
Liu, Li-Ming [1 ,2 ]
Zhang, Wei-Guo [1 ]
Xu, Jian-Zhong [1 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Key Lab Ind Biotechnol, Minist Educ, 1800 Lihu Rd, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Sch Biotechnol, State Key Lab Food Sci & Technol, 1800 Lihu Rd, Wuxi 214122, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Corynebacterium glutamicum; L-lysine production; Starch degradation; Amylolytic enzyme; Thermo-tolerance; ALPHA-AMYLASE; ESCHERICHIA-COLI; BETA-AMYLASE; BIFUNCTIONAL ENZYME; AMYLOLYTIC ENZYMES; SOLUBLE STARCH; YEAST-STRAIN; CELL-SURFACE; GENE; GLUCOAMYLASE;
D O I
10.1007/s00253-021-11714-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This article focuses on engineering Corynebacterium glutamicum to produce L-lysine efficiently from starch using combined method of "classical breeding" and "genome breeding." Firstly, a thermo-tolerable L-lysine-producing C. glutamicum strain KT45-6 was obtained after multi-round of acclimatization at high temperature. Then, amylolytic enzymes were introduced into strain KT45-6, and the resultant strains could use starch for cell growth and L-lysine production except the strain with expression of isoamylase. In addition, co-expression of amylolytic enzymes showed a good performance in starch degradation, cell growth and L-lysine production, especially co-expression of alpha-amylase (AA) and glucoamylase (GA). Moreover, L-lysine yield was increased by introducing AA-GA fusion protein (i.e., strain KT45-6S-5), and finally reached to 23.9 +/- 2.3 g/L in CgXII(IP)M-medium. It is the first report of an engineered L-lysine-producing strain with maximum starch utilization that may be used as workhorse for producing amino acid using starch as the main feedstock.
引用
收藏
页码:145 / 160
页数:16
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