Production of Tagatose by Whole-cell Bioconversion from Fructose Using Corynebacterium glutamicum

被引:15
作者
Jeon, Eun Jung [1 ,2 ]
Lee, Young-Mi [3 ]
Choi, Eun Jung [3 ]
Kim, Seong-Bo [3 ,4 ]
Jeong, Ki Jun [1 ,5 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Chem & Biomol Engn, BK Plus Program, Daejeon 34141, South Korea
[2] Korea Res Inst Biosci & Biotechnol KRIBB, Synthet Biol & Bioengn Res Inst, Synthet Biol Res Ctr, Daejeon 34141, South Korea
[3] CJ Cheiljedang Food Res Inst, Suwon 16495, South Korea
[4] Yonsei Univ, Global Leaders Coll, Seoul 03722, South Korea
[5] Korea Adv Inst Sci & Technol KAIST, Inst BioCentury, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
Corynebacterium glutamicum; tagatose; fructose; whole-cell biocatalyst; high copy plasmids; PLASMID COPY NUMBER; GENE-EXPRESSION; SECRETORY PRODUCTION; ANTISENSE-RNA; PLATFORM; BURDEN;
D O I
10.1007/s12257-022-0304-5
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
Tagatose is a rarely occurring sugar found in food and sweet fruits. It is a potential sweetener with low calories but a sweetness similar to that of sucrose. In this study, we developed a whole-cell biocatalyst using Corynebacterium glutamicum for direct bioconversion of fructose to tagatose. First, we constructed a biological conversion pathway for the conversion of fructose to tagatose by expressing tagatose 4-epimerase (TN) from Thermotoga neapolitana in C. glutamicum. Next, to increase the expression level of the enzyme, we engineered copy number of plasmid. Plasmid library was constructed by randomizing the cgrI antisense RNA region in the plasmid, and the plasmid with high-copy number was isolated using fluorescence-activated single cell sorting (FACS)-based high-throughput screening. The isolated plasmid, pHCP7, had 2-fold higher copy numbers than the original plasmid. A higher expression level and conversion yield could be achieved using pHCP7. Finally, we examined a novel tagatose 4-epimerase TN(KNF4E) isolated from Kosmotoga olearia. The gene expression level was further increased (33.9% of total fraction) through codon optimization and expression in pHCP7, and a conversion yield as high as 21.7% was achieved.
引用
收藏
页码:419 / 427
页数:9
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