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机构地区:[1]中国科学院上海植物生理研究所
出 处:《生物化学与生物物理学报》1998年第5期483-487,共5页
基 金:国家自然科学基金;植物分子遗传国家重点实验室基金
摘 要:利用突变引物和PCR方法对玉米叶绿体ATP合成酶的ε亚基进行定点突变,使ε亚基42位上的Thr分别替换成Cys、Arg、Ile和Pro。Thr变为Pro的ε亚基突变体不能表达,其他突变体与野生型一样,都能正常表达。Thr突变为Cys和Arg后,突变体对ATPase活力的抑制比野生型略高一些,但突变为Ile后,其抑制程度则极大地增强了。The effects of some residues in maize chloroplast ε subunit on its activity have been studied by site directed mutagenesis. After replacing Thr 42 of ε subunit with Cys, Arg, Ile or Pro, and forming the mutant εT42C, mutant εT42R, mutant εT42I and mutant εT42P respectively, it was found that the mutant εT42P protein could no longer be expressed, but expression of other ε subunit mutants was similar to that of wild type. Comparing the inhibitory potency of different mutants of ε subunit with that of the wild type, it was found that the inhibitory effects of ε subunit mutants εT42C and εT42R on ATPase activity were slightly higher than that of wild type, but the εT42I protein strongly inhibited the Ca 2+ ATPase activity.
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