Haraguchi K, Seki K, Kishimoto M, Nagata T, Kasumi T, Kainuma K, Kobayashi S
National Food Research Institute, Ministry of Agriculture, Forestry, and Fisheries, Ibaraki, Japan.
Biosci Biotechnol Biochem. 1995 Oct;59(10):1809-12. doi: 10.1271/bbb.59.1809.
A gene encoding an inulin fructotransferase (DFA I-producing) [EC 2.4.1.200] from Arthrobacter globiformis S14-3 was cloned and the nucleotides sequenced, for the first time. The sequence indicated that the native enzyme protein is composed of 392 amino acid residues. The native enzyme is an extracellar enzyme produced in the culture supernatant of A. globiformis S14-3, but the nucleotide sequence of the gene lacks a sequence for signal peptide for secretion. The 1.5-kb DNA fragment encoding the gene was found to produce the active enzyme in the culture supernatant of an E. coli clone, under the control of the lac promoter of pUC119.
首次克隆了来自球形节杆菌S14 - 3的编码菊粉果糖转移酶(产生DFA I)[EC 2.4.1.200]的基因并对其核苷酸进行了测序。序列表明天然酶蛋白由392个氨基酸残基组成。天然酶是在球形节杆菌S14 - 3培养上清液中产生的胞外酶,但该基因的核苷酸序列缺乏分泌信号肽序列。发现编码该基因的1.5kb DNA片段在pUC119的lac启动子控制下,能在大肠杆菌克隆的培养上清液中产生活性酶。