Pathway Construction in Corynebacterium glutamicum and Strain Engineering To Produce Rare Sugars from Glycerol

被引:27
作者
Yang, Jiangang [1 ]
Zhu, Yueming [1 ]
Men, Yan [1 ]
Sun, Shangshang [1 ]
Zeng, Yan [1 ]
Zhang, Ying [1 ]
Sun, Yuanxia [1 ]
Ma, Yanhe [1 ]
机构
[1] Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Natl Engn Lab Ind Enzymes, Tianjin 300308, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
rare sugars; aldolases; Corynebacterium glutamicum; metabolic engineering glycerol; ESCHERICHIA-COLI; SACCHAROMYCES-CEREVISIAE; ACID PRODUCTION; L-FRUCTOSE; L-PSICOSE; L-SORBOSE; BIOSYNTHESIS; DEHYDROGENASE; ISOMERASE; OVEREXPRESSION;
D O I
10.1021/acs.jafc.6b03423
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Rare sugars are valuable natural products widely used in pharmaceutical and food industries. In this study, we expected to synthesize rare ketoses from abundant glycerol using dihydroxyacetone phosphate (DHAP)-dependent aldolases. First, a new glycerol assimilation pathway was constructed to synthesize DHAP. The enzymes which convert glycerol to 3-hydroxypropionaldehyde and L-glyceraldehyde were selected, and their corresponding aldehyde synthesis pathways were constructed in vivo. Four aldol pathways based on different aldolases and phosphorylase were gathered. Next, three pathways were assembled and the resulting strains synthesized 5-deoxypsicose, 5-deoxysorbose, and 5-deoxyfructose from glucose and glycerol and produce L-fructose, L-tagatose, L-sorbose, and L-psicose with glycerol as the only carbon source. To achieve higher product titer and yield, the recombinant strains were further engineered and fermentation conditions were optimized. Fed-batch culture of engineered strains obtained 38.1 g/L 5-deoxypsicose with a yield of 0.91 +/- 0.04 mol product per mol of glycerol and synthesized 20.8 g/L L-fructose, 10.3 g/L L-tagatose, 1.2 g/L L-sorbose, and 0.95 g/L L-psicose.
引用
收藏
页码:9497 / 9505
页数:9
相关论文
共 44 条
[11]   L-nucleosides as chemotherapeutic agents [J].
Gumina, G ;
Song, GY ;
Chu, CK .
FEMS MICROBIOLOGY LETTERS, 2001, 202 (01) :9-15
[12]   Iminosugars past, present and future: medicines for tomorrow [J].
Home, Graeme ;
Wilson, Francis X. ;
Tinsley, Jon ;
Williams, David H. ;
Storer, Richard .
DRUG DISCOVERY TODAY, 2011, 16 (3-4) :107-118
[13]   Enzymatic production of L-tagatose and L-fructose from L-sorbose and L-psicose, respectively [J].
Itoh, H ;
Izumori, K .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1996, 81 (04) :351-353
[14]   Izumoring: A strategy for bioproduction of all hexoses [J].
Izumori, Ken .
JOURNAL OF BIOTECHNOLOGY, 2006, 124 (04) :717-722
[15]   Construction and application of new Corynebacterium glutamicum vectors [J].
Jakoby, M ;
Ngouoto-Nkili, CE ;
Burkovski, A .
BIOTECHNOLOGY TECHNIQUES, 1999, 13 (06) :437-441
[16]   Identification of a HAD superfamily phosphatase, HdpA, involved in 1,3-dihydroxyacetone production during sugar catabolism in Corynebacterium glutamicum [J].
Jojima, Toru ;
Igari, Takafumi ;
Gunji, Wataru ;
Suda, Masako ;
Inui, Masayuki ;
Yukawa, Hideaki .
FEBS LETTERS, 2012, 586 (23) :4228-4232
[17]   Elevated production of 3-hydroxypropionic acid by metabolic engineering of the glycerol metabolism in Escherichia coli [J].
Jung, Won Seok ;
Kang, Jin Ho ;
Chu, Hun Su ;
Choi, In Suk ;
Cho, Kwang Myung .
METABOLIC ENGINEERING, 2014, 23 :116-122
[18]   Tools for genetic engineering in the amino acid-producing bacterium Corynebacterium glutamicum [J].
Kirchner, O ;
Tauch, A .
JOURNAL OF BIOTECHNOLOGY, 2003, 104 (1-3) :287-299
[19]  
Kruger N J, 1994, Methods Mol Biol, V32, P9
[20]  
LEVIN GV, 1995, AM J CLIN NUTR, V62, P1161