|Table of Contents|

Expression of Functional Genes in Lignocellulose-dependent Lactic Acid Bacterium Pediococcus acidilactici DQ2(PDF)

Chinese Journal of Applied & Environmental Biology[ISSN:1006-687X/CN:51-1482/Q]

Issue:
2013 05
Page:
811-816
Research Field:
Articles
Publishing date:

Info

Title:
Expression of Functional Genes in Lignocellulose-dependent Lactic Acid Bacterium Pediococcus acidilactici DQ2
Author(s):
TU YiGAO QiuqiangBAO Jie
(State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China)
Keywords:
lignocellulose Pediococcus acidilactici DQ2 expression system promoter recombinant expression
CLC:
Q936 : Q786
PACS:
DOI:
10.3724/SP.J.1145.2013.00811
DocumentCode:

Abstract:
Pediococcus acidilactici DQ2, isolated by our lab, is thermotolerant and highly resistant to the inhibitors derived from lignocellulose, and can produce high titer of lactic acid. To construct the expression system of this strain, we modified the lactic acid bacterial expression vector pMG36e by replacing the promoter P32 with PldhL derived from P. acidilactici DQ2. Two different heterologous genes were expressed successfully with the new plasmid pTY36e: green fluorescent protein gene (gfp) from Aequorea victoria and β-glucosidase gene (bglA) from Bacillus polymyxa 1.794. The results showed β-glucosidase enzyme activity of the recombinant bacteria as 4.48 U g-1 (dry cells) detected in the intracellular fraction. The successful construction of this system lays the foundation for subsequent genetically engineering of P. acidilactici DQ2. Fig 4, Tab 3, Ref 25

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Last Update: 2013-10-28