Hibi Makoto, Sonoki Tomonori, Mori Hideo
Biofrontier Laboratories, Kyowa Hakko Kogyo Co. Ltd., 3-6-6 Asahimachi, Machidashi, Tokyo 194-8533, Japan.
FEMS Microbiol Lett. 2005 Dec 15;253(2):237-42. doi: 10.1016/j.femsle.2005.09.036. Epub 2005 Oct 10.
Pseudomonas putida vanillate-O-demethylase consisting of VanA and VanB was expressed in Escherichia coli strain K-12. Recombinant E. coli strain K-12 cells expressing VanAB efficiently converted vanillate into protocatechuate with glucose consumption. Mutant lacking either pgi or zwf showed higher or lower converting activity than the parental strain, respectively. Formaldehyde, which is the by-product of the demethylation, was converted into formate in the cellular reaction. Formate accumulation was blocked by gene disruption of the E. coli frmA that coded glutathione-dependent formaldehyde dehydrogenase.
由VanA和VanB组成的恶臭假单胞菌香草酸-O-脱甲基酶在大肠杆菌K-12菌株中表达。表达VanAB的重组大肠杆菌K-12细胞在消耗葡萄糖的情况下有效地将香草酸转化为原儿茶酸。缺乏pgi或zwf的突变体分别表现出比亲本菌株更高或更低的转化活性。脱甲基的副产物甲醛在细胞反应中转化为甲酸。甲酸积累被编码谷胱甘肽依赖性甲醛脱氢酶的大肠杆菌frmA基因破坏所阻断。