Ogawa Y, Tatsumi H, Murakami S, Ishida Y, Murakami K, Masaki A, Kawabe H, Arimura H, Nakano E, Motai H
Research and Development Division, Kikkoman Corporation, Chiba, Japan.
Agric Biol Chem. 1990 Oct;54(10):2521-9.
To produce Aspergillus oryzae alkaline protease (Alp) in an osmophilic yeast Zygosaccharomyces rouxii, we constructed an expression plasmid consisting of the Z. rouxii glyceraldehyde-3-phosphate dehydrogenase (GAPDH) promoter, the prepro-Alp cDNA of A. oryzae, the whole sequence of Z. rouxii plasmid pSR1, and the G418 resistant gene. The resulting plasmid, when introduced into Z. rouxii cells, directed the secretion of a large amount (about 300 mg/l) of Alp into the culture medium. The N-terminus and specific activity of the enzyme were identical to those of A. oryzae Alp.
为了在嗜渗酵母鲁氏接合酵母中生产米曲霉碱性蛋白酶(Alp),我们构建了一个表达质粒,该质粒由鲁氏接合酵母甘油醛-3-磷酸脱氢酶(GAPDH)启动子、米曲霉前原Alp cDNA、鲁氏接合酵母质粒pSR1的全序列以及G418抗性基因组成。将所得质粒导入鲁氏接合酵母细胞后,可将大量(约300 mg/l)的Alp分泌到培养基中。该酶的N端和比活性与米曲霉Alp相同。