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莱茵衣藻表达带有多组氨酸标签β亚基的叶绿体ATP合酶。

Expression by Chlamydomonas reinhardtii of a chloroplast ATP synthase with polyhistidine-tagged beta subunits.

作者信息

Johnson Eric A, Rosenberg Julian, McCarty Richard E

机构信息

Department of Biology, Johns Hopkins University, Baltimore, MD 21218-2685, USA.

出版信息

Biochim Biophys Acta. 2007 May;1767(5):374-80. doi: 10.1016/j.bbabio.2007.03.003. Epub 2007 Mar 15.

Abstract

The green alga Chlamydomonas reinhardtii is a model organism for the study of photosynthesis. The chloroplast ATP synthase is responsible for the synthesis of ATP during photosynthesis. Using genetic engineering and biolistic transformation, a string of eight histidine residues has been inserted into the amino-terminal end of the beta subunit of this enzyme in C. reinhardtii. The incorporation of these amino acids did not impact the function of the ATP synthase either in vivo or in vitro and the resulting strain of C. reinhardtii showed normal growth. The addition of these amino acids can be seen through altered gel mobility of the beta subunit and the binding of a polyhistidine-specific dye to the subunit. The purified his-tagged CF1 has normal Mg(2+)-ATPase activity, which can be stimulated by alcohol and detergents and the enzyme remains active while bound to a nickel-coated surface. Potential uses for this tagged enzyme as a biochemical tool are discussed.

摘要

绿藻莱茵衣藻是用于光合作用研究的模式生物。叶绿体ATP合酶负责光合作用过程中ATP的合成。利用基因工程和生物弹道转化技术,在莱茵衣藻中该酶的β亚基氨基末端插入了一串八个组氨酸残基。这些氨基酸的掺入在体内或体外均未影响ATP合酶的功能,所得的莱茵衣藻菌株生长正常。通过β亚基凝胶迁移率的改变以及多组氨酸特异性染料与该亚基的结合,可以看出这些氨基酸的添加。纯化的带有组氨酸标签的CF1具有正常的Mg(2+)-ATP酶活性,该活性可被酒精和去污剂刺激,并且该酶在与镍涂层表面结合时仍保持活性。讨论了这种带标签的酶作为生化工具的潜在用途。

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