Cloning and overexpression of the xylose isomerase gene from Burkholderia sacchari and production of polyhydroxybutyrate from xylose


Autoria(s): LOPES, Mateus Schreiner Garcez; GOMEZ, Jose Gregorio Cabrera; SILVA, Luiziana Ferreira
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

A different organization for the xyl operon was found in different genomes of Burkholderia and Pseudomomas species. Degenerated primers were designed based on Burkholderia genomes and used to amplify the xylose isomerase gene (xylA) from Burkholderia sacchari IPT101 The gene encoded a protein of 329 amino acids, which showed the highest similarity (90%) to the homologous gene of Burkholderia dolosa. It was cloned in the broad host range plasmid pBBR1MCS-2, which partially restored growth and polyhydroxybutyrate production capability in xylose to a B. sacchari xyl(-) mutant. When xylA was overexpressed in the wild-type strain, it was not able to increase growth and polyhydroxybutyrate production, suggesting that XylA activity is not limiting for xylose utilization in B. sacchari.

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[04/15369-0]

Identificador

CANADIAN JOURNAL OF MICROBIOLOGY, v.55, n.8, p.1012-1015, 2009

0008-4166

http://producao.usp.br/handle/BDPI/28451

10.1139/W09-055

http://dx.doi.org/10.1139/W09-055

Idioma(s)

eng

Publicador

NATL RESEARCH COUNCIL CANADA-N R C RESEARCH PRESS

Relação

Canadian Journal of Microbiology

Direitos

restrictedAccess

Copyright NATL RESEARCH COUNCIL CANADA-N R C RESEARCH PRESS

Palavras-Chave #xylose #xylose isomerase #xylA #Burkholderia sacchari #polyhydroxybutyrate #ZYMOMONAS-MOBILIS #ESCHERICHIA-COLI #ALCALIGENES-EUTROPHUS #RECOMBINANT STRAIN #FERMENTATION #GLUCOSE #BACTERIA #POLYHYDROXYALKANOATES #EXPRESSION #MIXTURES #Biochemistry & Molecular Biology #Biotechnology & Applied Microbiology #Immunology #Microbiology
Tipo

article

original article

publishedVersion