Woodson Jesse D, Escalante-Semerena Jorge C
Department of Bacteriology, University of Wisconsin, Madison, WI 53726-4087, USA.
Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3591-6. doi: 10.1073/pnas.0305939101. Epub 2004 Feb 27.
The existence of a pathway for salvaging the coenzyme B(12) precursor dicyanocobinamide (Cbi) from the environment was established by genetic and biochemical means. The pathway requires the function of a previously unidentified amidohydrolase enzyme that converts adenosylcobinamide to adenosylcobyric acid, a bona fide intermediate of the de novo coenzyme B(12) biosynthetic route. The cbiZ gene of the methanogenic archaeon Methanosarcina mazei strain Göl was cloned, was overproduced in Escherichia coli, and the recombinant protein was isolated to homogeneity. HPLC, UV-visible spectroscopy, MS, and bioassay data established adenosylcobyric as the corrinoid product of the CbiZ-catalyzed reaction. Inactivation of the cbiZ gene in the extremely halophilic archaeon Halobacterium sp. strain NRC-1 blocked the ability of this archaeon to salvage Cbi. cbiZ function restored Cbi salvaging in a strain of the bacterium Salmonella enterica, whose Cbi-salvaging pathway was blocked. The salvaging of Cbi through the CbiZ enzyme appears to be an archaeal strategy because all of the genomes of B(12)-producing archaea have a cbiZ ortholog. Reasons for the evolution of two distinct pathways for Cbi salvaging in prokaryotes are discussed.
通过遗传学和生物化学方法确定了从环境中挽救辅酶B12前体二氰钴胺素(Cbi)的途径。该途径需要一种先前未鉴定的酰胺水解酶发挥作用,该酶将腺苷钴胺素转化为腺苷钴胺酸,这是从头合成辅酶B12生物合成途径中的一个真正中间体。产甲烷古菌马氏甲烷八叠球菌菌株Göl的cbiZ基因被克隆,在大肠杆菌中过量表达,并且重组蛋白被纯化至同质。高效液相色谱、紫外可见光谱、质谱和生物测定数据确定腺苷钴胺酸是CbiZ催化反应的类咕啉产物。在极端嗜盐古菌盐生盐杆菌菌株NRC-1中cbiZ基因的失活阻断了该古菌挽救Cbi的能力。cbiZ功能恢复了肠道沙门氏菌菌株中Cbi的挽救,该菌株的Cbi挽救途径被阻断。通过CbiZ酶挽救Cbi似乎是一种古菌策略,因为所有产生B12的古菌基因组都有cbiZ直系同源物。讨论了原核生物中Cbi挽救的两种不同途径进化的原因。