Fujita Y, Takagi H, Hase T
Division of Enzymology, Osaka University, Japan.
Plant Cell Physiol. 1996 Apr;37(3):313-23. doi: 10.1093/oxfordjournals.pcp.a028948.
We cloned a 6.0-kb HindIII fragment from the cyanobacterium Plectonema boryanum using the chloroplast chlB (ORF513) gene of the liverwort (Marchantia polymorpha) as a probe. An open reading frame (ORF508) encoding a polypeptide of 508 amino acid residues was found within the nucleotide sequence of the 4,437-bp HindIII-EcoRV subfragment. The deduced amino acid sequence of ORF508 shows very high similarity to that encoded by the liverwort chlB gene (72.7%). A mutant, YFB14, in which ORF508 was inactivated by the insertion of a kanamycin-resistance cartridge, was unable to synthesize chlorophyll, accumulating protochlorophyllide in darkness while synthesizing chlorophyll normally in the light. Thus, the chlB gene is the third gene that is essential for the light-independent reduction of protochlorophyllide. The other two genes are chlL and chlN, and the results suggest that the light-independent protochlorophyllide reductase consists of at least three subunits, which are encoded by chlL, chlN and chlB. Using an antiserum prepared against a ChlB-6xHis fusion protein expressed in Escherichia coli, we detected a protein with an apparent molecular weight of 58,000 in the membrane fraction of the cyanobacterium. These results indicate that either the cytoplasmic or thylakoid membranes could be the site of the light-independent reduction of protochlorophyllide.
我们以地钱(Marchantia polymorpha)的叶绿体chlB(ORF513)基因作为探针,从蓝细菌Plectonema boryanum中克隆了一个6.0 kb的HindIII片段。在4437 bp的HindIII - EcoRV亚片段的核苷酸序列中发现了一个编码508个氨基酸残基多肽的开放阅读框(ORF508)。ORF508推导的氨基酸序列与地钱chlB基因编码的序列具有很高的相似性(72.7%)。一个突变体YFB14,其中ORF508因插入卡那霉素抗性盒而失活,在黑暗中无法合成叶绿素,积累原叶绿素酸酯,而在光照下能正常合成叶绿素。因此,chlB基因是原叶绿素酸酯光独立还原所必需的第三个基因。另外两个基因是chlL和chlN,结果表明光独立原叶绿素酸酯还原酶至少由三个亚基组成,分别由chlL、chlN和chlB编码。使用针对在大肠杆菌中表达的ChlB - 6xHis融合蛋白制备的抗血清,我们在蓝细菌的膜部分检测到一种表观分子量为58,000的蛋白质。这些结果表明细胞质膜或类囊体膜可能是原叶绿素酸酯光独立还原的位点。