Analysis of gene expression of bifidobacteria using as the reporter an anaerobic fluorescent protein.

Abstract:

OBJECTIVES:To determine the effectiveness of evoglow-Pp1 as a reporter to study gene expression in bifidobacteria. To choose a strong and constitutive promoter to track fluorescently labelled bifidobacteria in environments under anaerobic conditions. RESULTS:The elongation factor P (EF-P) promoter from Bifidobacterium longum CECT 4551 produced the highest emission of fluorescence signal and was therefore able to produce the highest gene expression of the promoters studied. The promoters from B. longum CECT 4551 showed different fluorescence signal intensities which, in descending order, were: EF-P, initiation factor IF-2, elongation factor G, elongation factor Tu, elongation factor Nus A, elongation factor Ts and 30S ribosomal protein S12. CONCLUSIONS:The consistency of the methods employed (fluorescence imaging system, fluorescence microscopy, fluorimetry and flow cytometry) showed that the construction pNZ:Prom.GFPana contained the anaerobic fluorescent protein evoglow-Pp1 could be exploited as a tool for analysing the gene expression in bifidobacteria strains.

journal_name

Biotechnol Lett

journal_title

Biotechnology letters

authors

Montenegro-Rodríguez C,Peirotén A,Sanchez-Jimenez A,Arqués JL,Landete JM

doi

10.1007/s10529-015-1802-8

subject

Has Abstract

pub_date

2015-07-01 00:00:00

pages

1405-13

issue

7

eissn

0141-5492

issn

1573-6776

journal_volume

37

pub_type

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