Adachi Osao, Ano Yoshitaka, Toyama Hirohide, Matsushita Kazunobu
Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, Japan.
Biosci Biotechnol Biochem. 2006 Oct;70(10):2579-82. doi: 10.1271/bbb.60259. Epub 2006 Oct 7.
3-Dehydroshikimate was formed with a yield of 57-77% from quinate via 3-dehydroquinate by two successive enzyme reactions, quinoprotein quinate dehydrogenase (QDH) and 3-dehydroquinate dehydratase, in the cytoplasmic membranes of acetic acid bacteria. 3-Dehydroshikimate was then reduced to shikimate (SKA) with NADP-dependent SKA dehydrogenase (SKDH) from the same organism. When SKDH was coupled with NADP-dependent D-glucose dehydrogenase (GDH) in the presence of excess D-glucose as an NADPH re-generating system, SKDH continued to produce SKA until 3-dehydroshikimate added initially in the reaction mixture was completely converted to SKA. Based on the data presented, a strategy for high SKA production was proposed.
在醋酸菌的细胞质膜中,奎尼酸通过两个连续的酶促反应,即喹蛋白奎尼酸脱氢酶(QDH)和3-脱氢奎尼酸脱水酶,经3-脱氢奎尼酸形成3-脱氢莽草酸,产率为57-77%。然后,来自同一生物体的依赖NADP的莽草酸脱氢酶(SKDH)将3-脱氢莽草酸还原为莽草酸(SKA)。当SKDH与依赖NADP的D-葡萄糖脱氢酶(GDH)在过量D-葡萄糖作为NADPH再生系统存在的情况下偶联时,SKDH持续产生SKA,直到最初添加到反应混合物中的3-脱氢莽草酸完全转化为SKA。基于所呈现的数据,提出了一种高产SKA的策略。