Yamano S, Tanaka J, Inoue T
Central Laboratory of Key Technology, Kirin Brewery Co., Ltd., Kanagawa, Japan.
J Biotechnol. 1994 Feb 14;32(2):165-71. doi: 10.1016/0168-1656(94)90179-1.
Acetobacter aceti ssp. xylinum genomic library was constructed using cosmid pJB8 in Escherichia coli. The gene encoding alpha-acetolactate decarboxylase (ALDC) was isolated from the library by direct measurement of ALDC activity. The ALDC gene was expressed by its own promoter in E. coli. The nucleotide sequence was determined, and an open reading frame which may encode a protein composed of 304 amino acids with a molecular weight of 33,747 was found. A brewer's yeast was transformed with the YEp-type plasmid containing the ALDC gene placed under the control of the glyceraldehyde-3-phosphate dehydrogenase promoter. The laboratory-scale growth test confirmed that the total diacetyl concentration was considerably reduced by the transformant. The analysis of the wort indicates that the Acetobacter ALDC reduces the concentration of diacetyl more effectively than that of 2,3-pentanedione.
使用黏粒pJB8在大肠杆菌中构建了醋化醋杆菌木糖氧化亚种基因组文库。通过直接测定α-乙酰乳酸脱羧酶(ALDC)活性,从该文库中分离出编码ALDC的基因。ALDC基因在大肠杆菌中由其自身启动子表达。测定了核苷酸序列,发现一个开放阅读框,其可能编码一种由304个氨基酸组成、分子量为33747的蛋白质。用含有置于甘油醛-3-磷酸脱氢酶启动子控制下的ALDC基因的YEp型质粒转化酿酒酵母。实验室规模的生长试验证实,转化体可显著降低双乙酰的总浓度。麦芽汁分析表明,醋化醋杆菌的ALDC比2,3-戊二酮更有效地降低双乙酰浓度。