Literature DB >> 9058966

Cloning of purine nucleoside phosphorylase II gene from Bacillus stearothermophilus TH 6-2 and characterization of its gene product.

T Hamamoto1, T Noguchi, Y Midorikawa.   

Abstract

Bacillus stearothermophilus TH 6-2 has two kinds of purine nucleoside phosphorylases (Pu-NPases). The type I enzyme (Pu-NPase I) is a functional and structural homolog of eukaryotic purine nucleoside phosphorylases that catalyze the phosphorolysis of inosine, guanosine, and their derivatives. The type II enzyme (Pu-NPase II) is a minor enzyme that efficiently phosphorolyzes adenosine and its derivatives rather than other purine nucleosides like Escherichia coli Pu-NPase. The gene coding for Pu-NPase II (punB gene) has been cloned and sequenced from TH 6-2 strain. The deduced amino acid sequence of Pu-NPase II shared 54% identity with that of E. coli enzyme, while it had no significant homology to that of Pu-NPase I or eukaryotic enzymes. By producing the Pu-NPase II in E. coli cells, the Pu-NPase II has been purified and characterized.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9058966     DOI: 10.1271/bbb.61.276

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  2 in total

1.  Enzymatic synthesis of nucleosides by nucleoside phosphorylase co-expressed in Escherichia coli.

Authors:  Qing-bao Ding; Ling Ou; Dong-zhi Wei; Xiao-kun Wei; Yan-mei Xu; Chun-yan Zhang
Journal:  J Zhejiang Univ Sci B       Date:  2010-11       Impact factor: 3.066

2.  Cloning, purification and characterisation of a recombinant purine nucleoside phosphorylase from Bacillus halodurans Alk36.

Authors:  Daniel F Visser; Fritha Hennessy; Konanani Rashamuse; Maureen E Louw; Dean Brady
Journal:  Extremophiles       Date:  2010-03       Impact factor: 2.395

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.