Liu H, Reynolds K A
Department of Medicinal Chemistry, Virginia Commonwealth University, Richmond, Virginia 23219, USA.
Metab Eng. 2001 Jan;3(1):40-8. doi: 10.1006/mben.2000.0169.
Crotonyl-CoA reductase (CCR), which catalyzes the reduction of crotonyl-CoA to butyryl-CoA, is common to most streptomycetes and appears to be inducible by either lysine or its catabolites in Streptomyces cinnamonensis grown in chemically defined medium. A major role of CCR in providing butyryl-CoA from acetate for monensin A biosynthesis has been demonstrated by the observation of a change in the monensin A/monensin B ratio in the parent C730.1 strain (50/50) and a ccr (encoding CCR) disruptant (12:88) of S. cinnamonensis in a complex medium. Both strains produce significantly higher monensin A/monensin B ratios in a chemically defined medium containing valine as a major carbon source than in either complex medium or chemically defined medium containing alternate amino acids. This observation demonstrates that under certain growth conditions valine catabolism may have a more significant role than CCR in providing butyryl-CoA. Such a process most likely involves an isomerization of the valine catabolite isobutyryl-CoA, catalyzed by the coenzyme B(12)-dependent isobutyryl-CoA mutase. Monensin labeling experiments using dual (13)C-labeled acetate in the ccr-disrupted S. cinnamonensis indicate the presence of an additional coenzyme B(12)-dependent mutase linking branched and straight-chain C(4) compounds by a new pathway.
巴豆酰辅酶A还原酶(CCR)催化巴豆酰辅酶A还原为丁酰辅酶A,在大多数链霉菌中都存在,并且在以化学限定培养基培养的肉桂链霉菌中,似乎可被赖氨酸或其分解代谢物诱导。通过观察肉桂链霉菌亲本C730.1菌株(50/50)和ccr(编码CCR)缺失突变体(12:88)在复合培养基中莫能菌素A/莫能菌素B比例的变化,已证明CCR在从乙酸盐提供丁酰辅酶A用于莫能菌素A生物合成中起主要作用。在以缬氨酸作为主要碳源的化学限定培养基中,这两种菌株产生的莫能菌素A/莫能菌素B比例均显著高于在复合培养基或含有其他氨基酸的化学限定培养基中。这一观察结果表明,在某些生长条件下,缬氨酸分解代谢在提供丁酰辅酶A方面可能比CCR发挥更重要的作用。这样一个过程很可能涉及由依赖辅酶B12的异丁酰辅酶A变位酶催化的缬氨酸分解代谢物异丁酰辅酶A的异构化。在ccr缺失的肉桂链霉菌中使用双(13)C标记乙酸盐的莫能菌素标记实验表明,存在一种额外的依赖辅酶B12的变位酶,它通过一条新途径连接支链和直链C4化合物。