Schlossman D, Withers D, Welsh P, Alexander A, Robertus J, Frankel A
Department of Medicine, Duke University Medical Center, Durham, North Carolina 22710.
Mol Cell Biol. 1989 Nov;9(11):5012-21. doi: 10.1128/mcb.9.11.5012-5021.1989.
The gene for the A chain of ricin toxin was fused to a beta-galactosidase marker cistron via a DNA sequence encoding a short collagen linker, and the tripartite fusion protein was expressed in Escherichia coli. Site-specific mutagenesis was used to change glutamic acid residue 177 to aspartic acid or alanine. When the mutant proteins were expressed, purified, and tested quantitatively for enzymatic activity, the carboxylate function at position 177 was found not to be absolutely essential for ricin toxin A-chain catalysis.
蓖麻毒素A链基因通过编码短胶原连接子的DNA序列与β-半乳糖苷酶标记顺反子融合,并且该三方融合蛋白在大肠杆菌中表达。利用定点诱变将谷氨酸残基177变为天冬氨酸或丙氨酸。当表达、纯化突变蛋白并对其酶活性进行定量检测时,发现177位的羧基功能对于蓖麻毒素A链催化并非绝对必要。