Nakayama M, Masuda T, Sato N, Yamagata H, Bowler C, Ohta H, Shioi Y, Takamiya K
Department of Biological Sciences, Faculty of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama, Japan.
Biochem Biophys Res Commun. 1995 Oct 4;215(1):422-8. doi: 10.1006/bbrc.1995.2481.
Mg-insertion is the first committed step in chlorophyll synthesis and is catalyzed by Mg-chelatase. In photosynthetic bacteria, bchI gene product was suggested to be a subunit of Mg-chelatase. We isolated a bchI homolog from a soybean cDNA library and designated it as chlI. CHLI consisted of 421 amino acid residues and the sequence exhibited a high similarity to other BchI homologs. CHLI contained an ATP-binding motif found in other BchI homologs. CHLI was localized in the soluble fraction in soybean chloroplasts, suggesting that it was a stromal subunit of Mg-chelatase. chlI mRNA in cell culture (SB-P) of soybean was reversibly induced by light.
镁插入是叶绿素合成的首个关键步骤,由镁螯合酶催化。在光合细菌中,bchI基因产物被认为是镁螯合酶的一个亚基。我们从大豆cDNA文库中分离出一个bchI同源物,并将其命名为chlI。CHLI由421个氨基酸残基组成,其序列与其他BchI同源物具有高度相似性。CHLI含有在其他BchI同源物中发现的ATP结合基序。CHLI定位于大豆叶绿体的可溶性部分,表明它是镁螯合酶的一个基质亚基。大豆细胞培养物(SB-P)中的chlI mRNA受光可逆诱导。