Boras G J, Au S, Roy K L, von Tigerstrom R G
Department of Microbiology, University of Alberta, Edmonton, Canada.
J Gen Microbiol. 1993 Jun;139 Pt 6:1245-52. doi: 10.1099/00221287-139-6-1245.
The gene for the periplasmic beta-lactamase of Lysobacter enzymogenes was isolated as part of a 1017 bp EcoRI fragment and the nucleotide sequence of the gene was determined. It has a G+C content of 71.5% and encodes a 27 amino acid signal sequence and the mature beta-lactamase of 276 amino acids which has a mass of 29,146 Da. The enzyme appears to be unique to L. enzymogenes but its amino acid sequence shows a high degree of homology with the amino acid sequences of the lactamase from Citrobacter diversus and other Class A beta-lactamases. The beta-lactamase gene of L. enzymogenes was expressed in Escherichia coli using pUC118 as the vector. The production of active beta-lactamase was highest after the active growth phase of the expression host and reached levels which were about three times higher than those obtained with L. enzymogenes.
产酶溶杆菌周质β-内酰胺酶基因作为一个1017bp的EcoRI片段的一部分被分离出来,并测定了该基因的核苷酸序列。其G+C含量为71.5%,编码一个27个氨基酸的信号序列和一个276个氨基酸的成熟β-内酰胺酶,该酶质量为29,146Da。该酶似乎是产酶溶杆菌所特有的,但其氨基酸序列与多样柠檬酸杆菌的内酰胺酶及其他A类β-内酰胺酶的氨基酸序列具有高度同源性。以pUC118为载体,产酶溶杆菌的β-内酰胺酶基因在大肠杆菌中得到表达。活性β-内酰胺酶的产量在表达宿主的活跃生长阶段之后最高,达到的水平比产酶溶杆菌所获得的水平高出约三倍。