Production of D-ribose by metabolically engineered Escherichia coli

被引:9
|
作者
Park, Hae-Chul [1 ]
Kim, Yun-Jung [2 ]
Lee, Chang-Wan [2 ]
Rho, Yong-Taek [2 ]
Kang, JeongWoo [1 ]
Lee, Dae-Hee [3 ]
Seong, Yeong-Je [4 ]
Park, Yong-Cheol [4 ]
Lee, Daesang [5 ]
Kim, Sung-Gun [2 ]
机构
[1] Anim & Plant Quarantine Agcy, Vet Drugs & Biol Div, Gyeongbuk 39660, South Korea
[2] Youngdong Univ, Dept Biomed Sci, Chungbuk 29131, South Korea
[3] KRIBB, Synthet Biol & Bioengn Res Ctr, Daejeon 34141, South Korea
[4] Kookmin Univ, Dept Bio & Fermentat Convergence Technol, Seoul 02707, South Korea
[5] Agcy Def Dev, R&D Inst 5 3, Daejeon 34188, South Korea
基金
新加坡国家研究基金会;
关键词
D-Ribose; Xylose; Escherichia coli; Transketolase; Catabolite repression; BACILLUS-SUBTILIS SPK1; ACID PRODUCTION; TRANSKETOLASE; DEFICIENT; GENE; GLUCOSE; XYLOSE; K-12; DISRUPTION; BIOMASS;
D O I
10.1016/j.procbio.2016.10.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Escherichia coli was metabolically engineered for the production of D-ribose, a functional five-carbon sugar, from xylose. For the accumulation of D-ribose, two genes of transketolase catalyzing the conversion of D-ribose-5-phosphate to sedoheptulose-7-phosphate in pentose phosphate pathway were disrupted to create a transketolase-deficient E. coli SGK013. In batch fermentation, E. coli SGKO13 grew by utilizing glucose and then started to produce D-ribose from xylose after glucose depletion. E. coli SGK013 produced 0.75 g/L of D-ribose, which was identical to the standard D-ribose as confirmed by HPLC and LC/MS analyses. To improve D-ribose production, the ptsG gene encoding the glucose-specific IICB component was disrupted additionally, resulting in the construction of E. coli SGK015. The carbon catabolite repression-negative E. colt SGK015 utilized xylose and glucose simultaneously and produced up to 3.75 g/L of D-ribose, which is a 5-fold improvement compared to that of E. colt SGK013. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:73 / 77
页数:5
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