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Development of recombinant Klebsiella pneumoniae ΔdhaT strain for the co-production of 3-hydroxypropionic acid and 1,3-propanediol from glycerol

机译:用于从甘油联产3-羟基丙酸和1,3-丙二醇的重组肺炎克雷伯氏菌ΔdhaT菌株的开发

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摘要

Klebsiella pneumoniae converts glycerol to the specialty chemical 1,3-propanediol (1,3-PDO), which is used for the production of polytrimethylene terepthalate (PTT). In this study, an NAD+-dependent gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (PuuC) of K. pneumoniae DSM 2026, which oxidizes 3-hydroxypropionaldehyde to a platform chemical 3-hydroxypropionic acid (3-HP), was cloned and overexpressed in K. pneumoniae DSM 2026 for the co-production of 3-HP and 1,3-PDO from glycerol. In addition, the gene dhaT, encoding NADH-dependent 1,3-propanediol oxidoreductase (1,3-PDOR), was deleted from the chromosome for the balanced production of 3-HP and 1,3-PDO. The recombinant K. pneumoniae ΔdhaT, expressing puuC, produced 3.6 g 3-HP and 3.0 g 1,3-PDO per liter with an average yield of 81% on glycerol carbon in shake flask culture under microaerobic conditions. When a fed-batch culture was carried out under microaerobic conditions at pH 7.0 in a 5-l bioreactor, the recombinant K. pneumoniae ΔdhaT (puuC) strain produced 16.0 g 3-HP and 16.8 g 1,3-PDO per liter with a cumulative yield of 51% on glycerol carbon in 24 h. The production of 1,3-PDO in the dhaT-deletion mutant was attributed to the expression of NAD(P)H-dependent hypothetical oxidoreductase. This study demonstrates the feasibility of obtaining two commercially valuable chemicals, 3-HP and 1,3-PDO, at a significant scale.
机译:肺炎克雷伯菌可将甘油转化为特殊化学物质1,3-丙二醇(1,3-PDO),用于生产聚对苯二甲酸丙二醇酯(PTT)。在这项研究中,克隆了NAD +依赖性肺炎克雷伯菌DSM 2026的NAD +依赖性γ-谷氨酰-γ-氨基丁醛脱氢酶(PuuC),该酶将3-羟基丙醛氧化为平台化学物质3-羟基丙酸(3-HP),并在其中过表达肺炎克雷伯氏菌DSM 2026,用于由甘油共同生产3-HP和1,3-PDO。此外,从染色体上删除了编码NADH依赖的1,3-丙二醇氧化还原酶(1,3-PDOR)的dhaT基因,以平衡产生3-HP和1,3-PDO。表达puuC的重组肺炎克雷伯菌ΔdhaT每升产生3.6 g 3-HP和3.0 g 1,3-PDO,在微有氧条件下摇瓶培养中甘油碳的平均产率为81%。当在5-l生物反应器中于pH 7.0的微有氧条件下进行分批补料培养时,重组肺炎克雷伯菌ΔdhaT(puuC)菌株每升产生16.0 g 3-HP和16.8 g 1,3-PDO,其中24小时内甘油碳的累计收率达51%。 dhaT缺失突变体中1,3-PDO的产生归因于NAD(P)H依赖的假设氧化还原酶的表达。这项研究证明了大规模获得两种具有商业价值的化学品3-HP和1,3-PDO的可行性。

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