Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on Glycerol

We analysed the draft genome sequence of Pseudomonas mediterranea CFBP 5447 in order to identify firstly the central metabolic pathways that convert fatty acids or carbohydrate intermediates into mcl-PHA and secondly the genes involved in glycerol metabolism (glpF, glpK, glpD, glpR). Absence of the...

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Main Authors: G. Licciardello, G. Devescovi, P. Bella, C. De Gregorio, A. Catara, S.P.P. Guglielmino, V. Venturi, V. Catara
Format: Article
Language:English
Published: AIDIC Servizi S.r.l. 2014-09-01
Series:Chemical Engineering Transactions
Online Access:https://www.cetjournal.it/index.php/cet/article/view/5654
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spelling doaj-95869928f78b464b9b733b3c7bc015d52021-02-20T21:20:34ZengAIDIC Servizi S.r.l.Chemical Engineering Transactions2283-92162014-09-013810.3303/CET1438049Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on GlycerolG. LicciardelloG. DevescoviP. BellaC. De GregorioA. CataraS.P.P. GuglielminoV. VenturiV. CataraWe analysed the draft genome sequence of Pseudomonas mediterranea CFBP 5447 in order to identify firstly the central metabolic pathways that convert fatty acids or carbohydrate intermediates into mcl-PHA and secondly the genes involved in glycerol metabolism (glpF, glpK, glpD, glpR). Absence of the glpF gene, which codifies for the “glycerol uptake facilitator protein”, was highlighted. In order to understand the expression of the pha gene cluster, we investigated the promoter activity of phaC1, phaC2, phaZ, phaD and phaI genes. When glycerol was present as the carbon source, PI was found to be the most active promoter. Expression analysis of the knock-out mutant of the phaD gene, which is a transcriptional regulator belonging to the TetR family, showed that PhaD acts as an activator of the phaI promoter which, in turn, triggers the transcription of the phaIF operon. The activation of PC1, which controls the phaC1ZC2D, by PhaD, was less efficient than PI.https://www.cetjournal.it/index.php/cet/article/view/5654
collection DOAJ
language English
format Article
sources DOAJ
author G. Licciardello
G. Devescovi
P. Bella
C. De Gregorio
A. Catara
S.P.P. Guglielmino
V. Venturi
V. Catara
spellingShingle G. Licciardello
G. Devescovi
P. Bella
C. De Gregorio
A. Catara
S.P.P. Guglielmino
V. Venturi
V. Catara
Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on Glycerol
Chemical Engineering Transactions
author_facet G. Licciardello
G. Devescovi
P. Bella
C. De Gregorio
A. Catara
S.P.P. Guglielmino
V. Venturi
V. Catara
author_sort G. Licciardello
title Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on Glycerol
title_short Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on Glycerol
title_full Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on Glycerol
title_fullStr Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on Glycerol
title_full_unstemmed Transcriptional Analysis of Pha Genes in Pseudomonas Mediterranea CFBP 5447 Grown on Glycerol
title_sort transcriptional analysis of pha genes in pseudomonas mediterranea cfbp 5447 grown on glycerol
publisher AIDIC Servizi S.r.l.
series Chemical Engineering Transactions
issn 2283-9216
publishDate 2014-09-01
description We analysed the draft genome sequence of Pseudomonas mediterranea CFBP 5447 in order to identify firstly the central metabolic pathways that convert fatty acids or carbohydrate intermediates into mcl-PHA and secondly the genes involved in glycerol metabolism (glpF, glpK, glpD, glpR). Absence of the glpF gene, which codifies for the “glycerol uptake facilitator protein”, was highlighted. In order to understand the expression of the pha gene cluster, we investigated the promoter activity of phaC1, phaC2, phaZ, phaD and phaI genes. When glycerol was present as the carbon source, PI was found to be the most active promoter. Expression analysis of the knock-out mutant of the phaD gene, which is a transcriptional regulator belonging to the TetR family, showed that PhaD acts as an activator of the phaI promoter which, in turn, triggers the transcription of the phaIF operon. The activation of PC1, which controls the phaC1ZC2D, by PhaD, was less efficient than PI.
url https://www.cetjournal.it/index.php/cet/article/view/5654
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