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豌豆(Pisum sativum)光合ATP合酶(EC 3.6.1.34)δ亚基cDNA的克隆与测序

Cloning and sequencing of a cDNA for the delta-subunit of photosynthetic ATP-synthase (EC 3.6.1.34) from pea (Pisum sativum).

作者信息

Hoesche J A, Berzborn R J

机构信息

Department of Biology, Lehrstuhl Biochemie der Pflanzen, Ruhr-Universität Bochum, Germany.

出版信息

Biochim Biophys Acta. 1992 Dec 29;1171(2):201-4. doi: 10.1016/0167-4781(92)90121-f.

Abstract

lambda gt10 cDNA clones for the nuclear encoded subunit delta of chloroplast ATP-synthase from Pisum sativum have been isolated. The 5' end was completed by PCR. The sequenced cDNA codes for the import precursor. N-Terminal sequencing of the mature protein isolated from chloroplasts revealed that the processing sites of the transit peptide from Pisum sativum and Spinacea oleracea are similar. The overall homology of the deduced amino acid sequences of the mature delta proteins from higher plants is about 40%. The conservation among hydrophilic residues is higher than for hydrophobic ones, indicating that the surface of delta is important for its function within the ATP-synthase.

摘要

已分离出豌豆叶绿体ATP合酶核编码亚基δ的λ gt10 cDNA克隆。通过PCR完成了5'端。测序的cDNA编码导入前体。对从叶绿体中分离出的成熟蛋白进行N端测序表明,豌豆和菠菜转运肽的加工位点相似。高等植物成熟δ蛋白推导氨基酸序列的总体同源性约为40%。亲水残基间的保守性高于疏水残基,表明δ亚基的表面对其在ATP合酶中的功能很重要。

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