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利用重组肺炎克雷伯氏菌 ∆dhaT 菌株从甘油共生产 3-羟基丙酸和 1,3-丙二醇。

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

机构信息

Department of Chemical and Biomolecular Engineering, International Affairs, Pusan National University, Busan, South Korea.

出版信息

Appl Microbiol Biotechnol. 2011 May;90(4):1253-65. doi: 10.1007/s00253-011-3148-z. Epub 2011 Feb 20.

Abstract

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 ∆dhaT, 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 ∆dhaT (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.

摘要

肺炎克雷伯氏菌将甘油转化为特种化学品 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,我们克隆并在肺炎克雷伯氏菌 DSM 2026 中过表达了一种依赖 NAD(+)的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品 3-羟基丙酸(3-HP),用于从甘油共生产 3-HP 和 1,3-PDO。此外,我们从染色体中删除了编码 NADH 依赖的 1,3-丙二醇氧化还原酶(1,3-PDOR)的基因 dhaT,以平衡 3-HP 和 1,3-PDO 的生产。表达 puuC 的重组肺炎克雷伯氏菌 ∆dhaT 在微氧条件下的摇瓶培养中,每升甘油碳可产生 3.6 g 3-HP 和 3.0 g 1,3-PDO,平均得率为 81%。在微氧条件下 pH 7.0 的 5 升生物反应器中进行分批补料培养时,重组肺炎克雷伯氏菌 ∆dhaT(puuC)菌株在 24 小时内每升甘油碳产生 16.0 g 3-HP 和 16.8 g 1,3-PDO,总得率为 51%。dhaT 缺失突变株中 1,3-PDO 的产生归因于 NAD(P)H 依赖的假定氧化还原酶的表达。本研究证明了以显著规模获得两种有商业价值的化学品 3-HP 和 1,3-PDO 的可行性。

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