Pathway Construction in <i>Corynebacterium glutamicum</i> and Strain Engineering To Produce Rare Sugars from Glycerol

甘油 二羟丙酮 达普 谷氨酸棒杆菌 磷酸二羟丙酮 甘油醛 生物化学 化学 醛缩酶A 果糖 山梨糖 代谢工程 发酵 羟醛反应 脱氢酶 催化作用 基因
作者
Jiangang Yang,Yueming Zhu,Yan Men,Shangshang Sun,Yan Zeng,Zhanqing Li,Yuanxia Sun,Yanhe Ma
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:64 (50): 9497-9505 被引量:18
标识
DOI:10.1021/acs.jafc.6b03423
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.
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