Method of using bacteriophage lambda p.sub.1 promoter to produce

Details Method of using bacteriophage lambda p.sub.1 promoter to produce Method of using bacteriophage lambda p.sub.1 promoter to produce

1984-09-27

1988-08-23

Martinell, James

Chemistry: molecular biology and microbiology

Micro-organism, tissue cell culture or enzyme using process...

Enzymatic production of a protein or polypeptide

435 91, 4351721, 4351723, 435253, 435320, 435886, 435889, 435896, 536 27, 935 29, 935 41, 935 43, 935 75, C12P 2100, C12P 1934, C12N 1500, C12N 120

Patent

active

047660660

ABSTRACT:
The invention relates to a method and cloning vehicle for the expression of a functional polypeptide in Streptomyces. A recombinant DNA cloning vehicle was genetically engineered to bring the expression of the neomycin phosphotransferase gene under the control of the Escherichia coli bacteriophage .lambda.p.sub.L promoter.

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