Lenz Oliver, Zebger Ingo, Hamann Josta, Hildebrandt Peter, Friedrich Bärbel
Humboldt-Universität zu Berlin, Institut für Biologie/Mikrobiologie, Chausseestrasse 117, Berlin, Germany.
FEBS Lett. 2007 Jul 10;581(17):3322-6. doi: 10.1016/j.febslet.2007.06.027. Epub 2007 Jun 21.
Within the catalytic centre of [NiFe]-hydrogenases one carbonyl and two cyanide ligands are covalently attached to the iron. To identify the metabolic origins of these ligands, the regulatory [NiFe] hydrogenase in conjunction with the indigenous Hyp maturation proteins of Ralstonia eutropha H16 were heterologously overproduced in E. coli grown in the presence of L-[ureido-(13)C] citrulline and NaH(13)CO(3). Infrared spectroscopy of purified hydrogenase provided direct evidence that only the cyanide ligands, but not the CO ligand, originate from CO(2) and carbamoylphosphate. Incorporation of label from (13)CO exclusively into the carbonyl ligand indicates that free CO is a possible precursor in carbonyl ligand biosynthesis.
在[NiFe]氢化酶的催化中心内,一个羰基和两个氰化物配体与铁共价连接。为了确定这些配体的代谢来源,在L-[脲基-(13)C]瓜氨酸和NaH(13)CO(3)存在下生长的大肠杆菌中,异源过量表达了调节性[NiFe]氢化酶以及真养产碱杆菌H16的原生Hyp成熟蛋白。纯化的氢化酶的红外光谱提供了直接证据,表明只有氰化物配体而非CO配体源自CO(2)和氨基甲酰磷酸。仅将(13)CO中的标记掺入羰基配体表明,游离CO可能是羰基配体生物合成中的前体。