首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Metabolic engineering of Klebsiella pneumoniae J2B for co-production of 3-hydroxypropionic acid and 1,3-propanediol from glycerol: Reduction of acetate and other by-products
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Metabolic engineering of Klebsiella pneumoniae J2B for co-production of 3-hydroxypropionic acid and 1,3-propanediol from glycerol: Reduction of acetate and other by-products

机译:Klebsiella肺炎的代谢工程J2B用于共产生3-羟基丙酸和1,3-丙二醇的甘油:乙酸盐还原及其他副产物

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摘要

Production of 3-hydroxypropionic acid (3-HP) or 1,3-propanediol (1,3-PDO) production from glycerol is challenging due to the problems associated with cofactor regeneration, coenzyme B12 synthesis, and the instability of pathway enzymes. To address these complications, simultaneous production of 3-HP and 1,3-PDO, instead of individual production of each compound, was attempted. With over-expression of an aldehyde dehydrogenase, recombinant Klebsiella pneumoniae could co-produce 3-HP and 1,3-PDO successfully. However, the production level was unsatisfactory due to excessive accumulation of many by-products, especially acetate. To reduce acetate production, we attempted; (i) reduction of glycerol assimilation through the glycolytic pathway, (ii) increase of glycerol flow towards co-production, and (iii) variation of aeration rate. These efforts were partially beneficial in reducing acetate and improving co-production: 21 g/L of 1,3-PDO and 43 g/L of 3-HP were obtained. Excessive acetate (> 150 mM) was still produced at the end of bioreactor runs, and limited co-production efficiency.
机译:由于与辅因子再生,辅酶B12合成相关的问题,来自甘油的3-羟基丙酸(3-HP)或1,3-PDO)产生的3-羟基丙酸(3-HP)或1,3-PDO)的产生是挑战性的。为了解决这些并发症,尝试同时生产3-HP和1,3-PDO,而不是每个化合物的单独生产。随着醛脱氢酶的过度表达,重组克莱布氏菌肺炎可以成功共同生产3-HP和1,3-PDO。然而,由于许多副产品的过度积累,尤其是醋酸盐,生产水平令人不令人满意。为了减少醋酸盐,我们试图; (i)通过甘油途径的降低甘油同化,(ii)甘油流动朝向共产生的增加,以及(iii)曝气率的变化。这些努力在减少乙酸盐和改善的共产生方面是部分有益的:21g / L 1,3-PDO和43克/升3-HP。在生物反应器的末端仍然产生过量的乙酸盐(> 150mm),并且有限的合成效率。

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