Schellenberg G D, Sarthy A, Larson A E, Backer M P, Crabb J W, Lidstrom M, Hall B D, Furlong C E
J Biol Chem. 1984 Jun 10;259(11):6826-32.
The gene that codes for xylose isomerase in Escherichia coli has been cloned by complementation of a xylose isomerase-negative E. coli mutant. The structural gene is 1320 nucleotides in length and codes for a protein of 440 amino acids. An additional 209 nucleotides 5' and 82 nucleotides 3' to the structural gene were also sequenced. To verify that the cloned gene encodes E. coli xylose isomerase, the enzyme was purified to homogeneity and the sequence of the first 25 amino acid residues was determined by a semimicromanual Edman procedure. These results establish that the NH2-terminal methionine of xylose isomerase is specified by an ATG which is 7 nucleotides downstream from a Shine-Dalgarno sequence.
通过对木糖异构酶阴性的大肠杆菌突变体进行互补,已克隆出大肠杆菌中编码木糖异构酶的基因。该结构基因长度为1320个核苷酸,编码一个由440个氨基酸组成的蛋白质。还对结构基因5'端额外的209个核苷酸和3'端的82个核苷酸进行了测序。为了验证克隆的基因编码大肠杆菌木糖异构酶,将该酶纯化至同质,并通过半微量手动埃德曼法确定了前25个氨基酸残基的序列。这些结果表明,木糖异构酶的NH2端甲硫氨酸由一个位于Shine-Dalgarno序列下游7个核苷酸处的ATG指定。