scholarly journals Transcriptional analysis of the effect of exogenous decanoic acid stress on Streptomyces roseosporus

2013 ◽  
Vol 12 (1) ◽  
pp. 19 ◽  
Author(s):  
Guojian Liao ◽  
Qing Liu ◽  
Jianping Xie
2005 ◽  
Vol 51 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Fredrik Karlsson ◽  
Ann-Christin Malmborg-Hager ◽  
Ann-Sofie Albrekt ◽  
Carl A.K Borrebaeck

To identify Escherichia coli genes potentially regulated by filamentous phage infection, we used oligonucleotide microarrays. Genome-wide comparison of phage M13-infected and uninfected E. coli, 2 and 20 min after infection, was performed. The analysis revealed altered transcription levels of 12 E. coli genes in response to phage infection, and the observed regulation of phage genes correlated with the known in vivo pattern of M13 mRNA species. Ten of the 12 host genes affected could be grouped into 3 different categories based on cellular function, suggesting a coordinated response. The significantly upregulated genes encode proteins involved in reactions of the energy-generating phosphotransferase system and transcription processing, which could be related to phage transcription. No genes belonging to any known E. coli stress response pathways were scored as upregulated. Furthermore, phage infection led to significant downregulation of transcripts of the bacterial genes gadA, gadB, hdeA, gadE, slp, and crl. These downregulated genes are normally part of the host stress response mechanisms that protect the bacterium during conditions of acid stress and stationary phase transition. The phage-infected cells demonstrated impaired function of the oxidative and the glutamate-dependent acid resistance systems. Thus, global transcriptional analysis and functional analysis revealed previously unknown host responses to filamentous phage infection.Key words: filamentous phage infection, global transcriptional analysis, AR, Escherichia coli.


PLoS ONE ◽  
2013 ◽  
Vol 8 (7) ◽  
pp. e68470 ◽  
Author(s):  
Ana Lúcia Carvalho ◽  
David L. Turner ◽  
Luís L. Fonseca ◽  
Ana Solopova ◽  
Teresa Catarino ◽  
...  

2015 ◽  
Vol 45 ◽  
pp. 71-82 ◽  
Author(s):  
Alexander Ter Beek ◽  
Janneke G.E. Wijman ◽  
Anna Zakrzewska ◽  
Rick Orij ◽  
Gertien J. Smits ◽  
...  

2006 ◽  
Vol 52 (7) ◽  
pp. 617-622 ◽  
Author(s):  
Aurélie Budin-Verneuil ◽  
Emmanuelle Maguin ◽  
Yanick Auffray ◽  
Dusko S Ehrlich ◽  
Vianney Pichereau

In a recent proteomic analysis, we showed the overproduction of the ArcA and ArcB proteins in Lactococcus lactis MG1363 at low pH. The corresponding genes belong to the arcABD1C1C2TD2 cluster that encodes components of the arginine deiminase pathway. In this study, we characterized this cluster at the genetic level. Northern blot experiments showed the expression of at least seven transcripts, all induced by acidity. Tran script analysis using 5′RACE PCR (rapid amplification of cDNA ends polymerase chain reaction) in the arcB-arcD1intergenic region. In silico analysis identified nine stem-loop structures, all located in intergenic regions. Collectively, these data suggest a role for RNA processing and (or) premature termination in the differential expression of genes within the arcABD1C1C2TD2 cluster.Key words: lactic acid bacteria, acid stress, arginine catabolism.


2016 ◽  
Vol 122 (4) ◽  
pp. 427-433 ◽  
Author(s):  
Sung-Kwon Lee ◽  
Hong Rip Kim ◽  
Ying-Yu Jin ◽  
Seung Hwan Yang ◽  
Joo-Won Suh

2010 ◽  
Vol 76 (22) ◽  
pp. 7526-7535 ◽  
Author(s):  
J. L. Legras ◽  
C. Erny ◽  
C. Le Jeune ◽  
M. Lollier ◽  
Y. Adolphe ◽  
...  

ABSTRACT Medium-chain fatty acids (octanoic and decanoic acids) are well known as fermentation inhibitors. During must fermentation, the toxicity of these fatty acids is enhanced by ethanol and low pH, which favors their entrance in the cell, resulting in a decrease of internal pH. We present here the characterization of the mechanisms involved in the establishment of the resistance to these fatty acids. The analysis of the transcriptome response to the exposure to octanoic and decanoic acids revealed that two partially overlapping mechanisms are activated; both responses share many genes with an oxidative stress response, but some key genes were activated differentially. The transcriptome response to octanoic acid stress can be described mainly as a weak acid response, and it involves Pdr12p as the main transporter. The phenotypic analysis of knocked-out strains confirmed the role of the Pdr12p transporter under the control of WAR1 but also revealed the involvement of the Tpo1p m ajor f acilitator s uperfamily proteins (MFS) transporter in octanoic acid expulsion. In contrast, the resistance to decanoic acid is composite. It also involves the transporter Tpo1p and includes the activation of several genes of the beta-oxidation pathway and ethyl ester synthesis. Indeed, the induction of FAA1 and EEB1, coding for a long-chain fatty acyl coenzyme A synthetase and an alcohol acyltransferase, respectively, suggests a detoxification pathway through the production of decanoate ethyl ester. These results are confirmed by the sensitivity of strains bearing deletions for the transcription factors encoded by PDR1, STB5, OAF1, and PIP2 genes.


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