scholarly journals Catabolite Repression of Pseudomonas aeruginosa Amidase: The Effect of Carbon Source on Amidase Synthesis

1975 ◽  
Vol 90 (1) ◽  
pp. 81-90 ◽  
Author(s):  
P. F. SMYTH ◽  
P. H. CLARKE
2012 ◽  
Vol 78 (14) ◽  
pp. 5016-5020 ◽  
Author(s):  
Jiaofang Huang ◽  
Elisabeth Sonnleitner ◽  
Bin Ren ◽  
Yuquan Xu ◽  
Dieter Haas

ABSTRACTInPseudomonas aeruginosa, the catabolite repression control (Crc) protein repressed the formation of the blue pigment pyocyanin in response to a preferred carbon source (succinate) by interacting withphzMmRNA, which encodes a key enzyme in pyocyanin biosynthesis. Crc bound to an extended imperfect recognition sequence that was interrupted by the AUG translation initiation codon.


2001 ◽  
Vol 44 (4) ◽  
pp. 183-188 ◽  
Author(s):  
F. J. Almendariz ◽  
M. Meráz ◽  
G. Soberón ◽  
O. Monroy

The degradation of of lineal alkylbenzene sulphonate (LAS) was studied in a two-stage anaerobic system where the acidogenic reactor was bioaugmented with a strain of Pseudomonas aeruginosa (M113). This is a strain, which under aerobic and denitrifying conditions uses LAS as carbon source. Results show that LAS was only degraded within the acidogenic stage while in the methanogenic reactor there was no degradation and eventually there was an inhibition due to a LAS accumulation in the sludge. During the experiment, the M113 strain remained in the acidogenic conglomerate (at around 104 CFU/mL) although there is no evidence of their involvement in LAS degradation.


2020 ◽  
Vol 367 (10) ◽  
Author(s):  
Rodolfo García-Contreras ◽  
Daniel Loarca ◽  
Caleb Pérez-González ◽  
J Guillermo Jiménez-Cortés ◽  
Abigail Gonzalez-Valdez ◽  
...  

ABSTRACT Pseudomonas aeruginosa is one of the main models to study social behaviors in bacteria since it synthesizes several exoproducts, including exoproteases and siderophores and release them to the environment. Exoproteases and siderophores are public goods that can be utilized by the individuals that produce them but also by non-producers, that are considered social cheaters. Molecularly exoprotease cheaters are mutants in regulatory genes such as lasR, and are commonly isolated from chronic infections and selected in the laboratory upon serial cultivation in media with protein as a sole carbon source. Despite that the production of exoproteases is exploitable, cooperators have also ways to restrict the growth and selection of social cheaters, for instance by producing toxic metabolites like pyocyanin. In this work, using bacterial competitions, serial cultivation and growth assays, we demonstrated that rhamnolipids which production is regulated by quorum sensing, selectively affect the growth of lasR mutants and are able to restrict social cheating, hence contributing to the maintenance of cooperation in Pseudomonas aeruginosa populations.


1997 ◽  
Vol 43 (5) ◽  
pp. 432-439 ◽  
Author(s):  
Stuart M. Pitson ◽  
Robert J. Seviour ◽  
Barbara M. McDougall

The effect of carbon source on the levels of three (1 → 3)-β-glucanases and a (1 → 6)-β-glucanase in the culture filtrates of the filamentous fungus Acremonium persicinum was investigated. All four enzymes were produced during growth of the fungus on (1 → 3)-, (1 → 6)-, and (1 → 3)(1 → 6)-β-glucans as well as β-linked oligoglucosides. However, only one (1 → 3)-β-glucanase and the (1 → 6)-β-glucanase were detected during growth on a range of other carbon sources including glucose, carboxymethylcellulose, and the α-glucan pullulan. The presence of glucose in the medium markedly decreased the production of all four glucanases, although the concentration required to effect complete repression of enzyme levels varied for the different enzymes. Similar repressive effects were also observed with sucrose, fructose, and galactose. The most likely explanations for these observations are that the synthesis of the (1 → 6)-β-glucanase and one of the (1 → 3)-β-glucanases is controlled by carbon catabolite repression, while the remaining two (1 → 3)-β-glucanases are inducible enzymes subject to carbon catabolite repression.Key words: (1 → 3)-β-glucanase, (1 → 6)-β-glucanase, Acremonium persicinum, regulation of synthesis, fungal β-glucanases.


2011 ◽  
Vol 8 (3) ◽  
pp. 471-482 ◽  
Author(s):  
S. A. Medina-Moreno ◽  
D. Jiménez-Islas ◽  
J. N. Gracida-Rodríguez ◽  
M. Gutiérrez-Rojas ◽  
I. J. Díaz-Ramírez

2017 ◽  
Vol 39 ◽  
pp. 36-41 ◽  
Author(s):  
Marco S. Nicolò ◽  
Maria G. Cambria ◽  
Giuseppe Impallomeni ◽  
Maria G. Rizzo ◽  
Cinzia Pellicorio ◽  
...  

mBio ◽  
2018 ◽  
Vol 9 (3) ◽  
Author(s):  
Leandro José de Assis ◽  
Mevlut Ulas ◽  
Laure Nicolas Annick Ries ◽  
Nadia Ali Mohamed El Ramli ◽  
Ozlem Sarikaya-Bayram ◽  
...  

ABSTRACTThe attachment of one or more ubiquitin molecules by SCF (Skp–Cullin–F-box) complexes to protein substrates targets them for subsequent degradation by the 26S proteasome, allowing the control of numerous cellular processes. Glucose-mediated signaling and subsequent carbon catabolite repression (CCR) are processes relying on the functional regulation of target proteins, ultimately controlling the utilization of this carbon source. In the filamentous fungusAspergillus nidulans, CCR is mediated by the transcription factor CreA, which modulates the expression of genes encoding biotechnologically relevant enzymes. Although CreA-mediated repression of target genes has been extensively studied, less is known about the regulatory pathways governing CCR and this work aimed at further unravelling these events. The Fbx23 F-box protein was identified as being involved in CCR and the Δfbx23mutant presented impaired xylanase production under repressing (glucose) and derepressing (xylan) conditions. Mass spectrometry showed that Fbx23 is part of an SCF ubiquitin ligase complex that is bridged via the GskA protein kinase to the CreA-SsnF-RcoA repressor complex, resulting in the degradation of the latter under derepressing conditions. Upon the addition of glucose, CreA dissociates from the ubiquitin ligase complex and is transported into the nucleus. Furthermore, casein kinase is important for CreA function during glucose signaling, although the exact role of phosphorylation in CCR remains to be determined. In summary, this study unraveled novel mechanistic details underlying CreA-mediated CCR and provided a solid basis for studying additional factors involved in carbon source utilization which could prove useful for biotechnological applications.IMPORTANCEThe production of biofuels from plant biomass has gained interest in recent years as an environmentally friendly alternative to production from petroleum-based energy sources. Filamentous fungi, which naturally thrive on decaying plant matter, are of particular interest for this process due to their ability to secrete enzymes required for the deconstruction of lignocellulosic material. A major drawback in fungal hydrolytic enzyme production is the repression of the corresponding genes in the presence of glucose, a process known as carbon catabolite repression (CCR). This report provides previously unknown mechanistic insights into CCR through elucidating part of the protein-protein interaction regulatory system that governs the CreA transcriptional regulator in the reference organismAspergillus nidulansin the presence of glucose and the biotechnologically relevant plant polysaccharide xylan.


Sign in / Sign up

Export Citation Format

Share Document