Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing, 210037, People's Republic of China.
College of Chemical Engineering, Nanjing Forestry University, Nanjing, 210037, People's Republic of China.
Bioprocess Biosyst Eng. 2018 Aug;41(8):1205-1212. doi: 10.1007/s00449-018-1949-5. Epub 2018 Jun 22.
Phenyllactic acid (PLA) is a high-value compound, which was usually produced by lactic acid bacteria (LAB) as biocatalysts and glucose or phenylpyruvic acid (PPA) as starting materials for PLA synthesis in previous studies. However, the PLA produced using LAB is a racemic mixture. Besides, both glucose and PPA were unsatisfactory substrates, as the former could not produce high concentrations of PLA while the latter is not a renewable and green substrate. To overcome these drawbacks, in this study, a new biotransformation process was developed for chiral PLA production from L-phenylalanine via the intermediate PPA using recombinant Escherichia coli co-expressing L-amino acid deaminase, NAD-dependent L-lactate dehydrogenase or NAD-dependent D-lactate dehydrogenase, and formate dehydrogenase. After optimization, the recombinant E. coli produced L- and D-PLA at concentrations of 59.9 and 60.3 mM in 6 h, respectively. Hence, this process provides an effective and promising alternative method for chiral PLA production.
苯乳酸(PLA)是一种高附加值的化合物,在以往的研究中,通常使用乳酸细菌(LAB)作为生物催化剂,以葡萄糖或苯丙酮酸(PPA)作为 PLA 合成的起始原料来生产 PLA。然而,使用 LAB 生产的 PLA 是外消旋混合物。此外,葡萄糖和 PPA 都不是理想的底物,前者不能产生高浓度的 PLA,而后者不是可再生和绿色的底物。为了克服这些缺点,在本研究中,通过重组大肠杆菌共表达 L-氨基酸脱氨酶、NAD 依赖性 L-乳酸脱氢酶或 NAD 依赖性 D-乳酸脱氢酶和甲酸脱氢酶,从 L-苯丙氨酸经中间体 PPA 开发了一种新的手性 PLA 生产生物转化工艺。经过优化,重组大肠杆菌在 6 小时内分别产生了 59.9 和 60.3mM 的 L-和 D-PLA。因此,该工艺为手性 PLA 的生产提供了一种有效且有前景的替代方法。