Literature DB >> 2120717

Use of the tyrosinase gene from Streptomyces to probe promoter sequences for Escherichia coli.

M Sugiyama1, H Nomura, O Nimi.   

Abstract

We have constructed a promoter-probe vector utilizing the expression of a promoter-less tyrosinase derived from Streptomyces plasmid pIJ702. The vector, pMX100, has single sites for EcoRI, KpnI, BamHI, XbaI, SalI, and SphI for cloning promoter sequences. When the tac promoter was inserted into pMX100, E. coli harboring the chimeric plasmid produced the melanin pigment.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2120717     DOI: 10.1016/0147-619x(90)90055-h

Source DB:  PubMed          Journal:  Plasmid        ISSN: 0147-619X            Impact factor:   3.466


  3 in total

1.  Cloning and sequence analysis of the highly expressed melanin-synthesizing gene operon from Streptomyces castaneoglobisporus.

Authors:  K Ikeda; T Masujima; K Suzuki; M Sugiyama
Journal:  Appl Microbiol Biotechnol       Date:  1996-03       Impact factor: 4.813

2.  Expression of cho and melC operons by a Streptococcus thermophilus synthetic promoter in Escherichia coli.

Authors:  D K Solaiman; G A Somkuti
Journal:  Appl Microbiol Biotechnol       Date:  1995 May-Jun       Impact factor: 4.813

3.  Expression of Streptomyces melC and choA genes by a cloned Streptococcus thermophilus promoter STP2201.

Authors:  D K Solaiman; G A Somkuti
Journal:  J Ind Microbiol       Date:  1995-07
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.