...
首页> 外文期刊>Applied and Environmental Microbiology >Efficient Homolactic Fermentation byKluyveromyces lactis Strains Defective in Pyruvate Utilization and Transformed with the HeterologousLDH Gene
【24h】

Efficient Homolactic Fermentation byKluyveromyces lactis Strains Defective in Pyruvate Utilization and Transformed with the HeterologousLDH Gene

机译:丙酮酸克鲁维酵母菌株有效丙酮酸发酵在丙酮酸利用方面有缺陷,并用异源LDH基因转化

获取原文

摘要

A high yield of lactic acid per gram of glucose consumed and the absence of additional metabolites in the fermentation broth are two important goals of lactic acid production by microrganisms. Both purposes have been previously approached by using aKluyveromyces lactis yeast strain lacking the single pyruvate decarboxylase gene (KlPDC1) and transformed with the heterologous lactate dehydrogenase gene (LDH). The LDH gene was placed under the control theKlPDC1 promoter, which has allowed very high levels of lactate dehydrogenase (LDH) activity, due to the absence of autoregulation by KlPdc1p. The maximal yield obtained was 0.58 g g?1, suggesting that a large fraction of the glucose consumed was not converted into pyruvate. In a different attempt to redirect pyruvate flux toward homolactic fermentation, we usedK. lactis LDH transformant strains deleted of the pyruvate dehydrogenase (PDH) E1α subunit gene. A great process improvement was obtained by the use of producing strains lacking both PDH and pyruvate decarboxylase activities, which showed yield levels of as high as 0.85 g g?1 (maximum theoretical yield, 1 g g?1), and with high LDH activity.
机译:每克消耗的葡萄糖中乳酸的高产量以及发酵液中不存在其他代谢物是微生物生产乳酸的两个重要目标。先前已经通过使用缺少单个丙酮酸脱羧酶基因(K1PDC1)并用异源乳酸脱氢酶基因(LDH)转化的乳酸克鲁维酵母菌株来实现这两个目的。 LDH基因置于KlPDC1启动子的控制之下,由于没有KlPdc1p的自动调节,该启动子允许很高水平的乳酸脱氢酶(LDH)活性。所获得的最大产量为0.58克/克1,表明所消耗的大部分葡萄糖没有转化为丙酮酸。在另一种尝试将丙酮酸通量重定向至同型发酵中,我们使用了K。乳酸LDH转化菌株删除了丙酮酸脱氢酶(PDH)E1α亚基基因。通过使用既缺乏PDH又没有丙酮酸脱羧酶活性的生产菌株获得了很大的工艺改进,该菌株显示出高达0.85g g?1的产量(最大理论产量为1g g?1),并且具有高的LDH活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号