Sato S, Nakada Y, Kanaya S, Tanaka T
Mitsubishi-Kasei Institute of Life Sciences, Tokyo, Japan.
Biochim Biophys Acta. 1988 Sep 7;950(3):303-12. doi: 10.1016/0167-4781(88)90126-1.
The trpE gene of Thermus thermophilus HB8 was cloned by complementation of an Escherichia coli tryptophan auxotroph. The E. coli harboring the cloned gene produced the anthranilate synthase I, which was heat-stable and enzymatically active at higher temperature. The nucleotide sequence of the trpE gene and its flanking regions was determined. The trpE gene was preceded by an attenuator-like structure and followed by the trpG gene, with a short gap between them. No other gene essential for tryptophan biosynthesis was observed after the trpG gene. The amino-acid sequences of the T. themophilus anthranilate synthase I and II deduced from the nucleotide sequence were compared with those of other organisms.
嗜热栖热菌HB8的trpE基因通过对大肠杆菌色氨酸营养缺陷型的互补作用进行克隆。携带克隆基因的大肠杆菌产生了邻氨基苯甲酸合酶I,该酶具有热稳定性且在较高温度下具有酶活性。测定了trpE基因及其侧翼区域的核苷酸序列。trpE基因之前有一个类似衰减子的结构,之后是trpG基因,它们之间有一个小间隔。在trpG基因之后未观察到其他色氨酸生物合成必需的基因。将从核苷酸序列推导的嗜热栖热菌邻氨基苯甲酸合酶I和II与其他生物的氨基酸序列进行了比较。