The conversion of the nutrient condition alter the phenol degradation pathway by Rhodococcus biphenylivorans B403: A comparative transcriptomic and proteomic approach

Author(s):  
Xiaohang Xie ◽  
Jiashu Liu ◽  
Zhengbing Jiang ◽  
Huanan Li ◽  
Meng Ye ◽  
...  
2012 ◽  
Vol 197 (2) ◽  
pp. 219-230 ◽  
Author(s):  
Florian Steinberg ◽  
Kate J. Heesom ◽  
Mark D. Bass ◽  
Peter J. Cullen

The FERM-like domain–containing sorting nexins of the SNX17/SNX27/SNX31 family have been proposed to mediate retrieval of transmembrane proteins from the lysosomal pathway. In this paper, we describe a stable isotope labeling with amino acids in culture–based quantitative proteomic approach that allows an unbiased, global identification of transmembrane cargoes that are rescued from lysosomal degradation by SNX17. This screen revealed that several integrins required SNX17 for their stability, as depletion of SNX17 led to a loss of β1 and β5 integrins and associated a subunits from HeLa cells as a result of increased lysosomal degradation. SNX17 bound to the membrane distal NPXY motif in β integrin cytoplasmic tails, thereby preventing lysosomal degradation of β integrins and their associated a subunits. Furthermore, SNX17-dependent retrieval of integrins did not depend on the retromer complex. Consistent with an effect on integrin recycling, depletion of SNX17 also caused alterations in cell migration. Our data provide mechanistic insight into the retrieval of internalized integrins from the lysosomal degradation pathway, a prerequisite for subsequent recycling of these matrix receptors.


2003 ◽  
Vol 46 (4) ◽  
pp. 537-543 ◽  
Author(s):  
Eliska Komarkova ◽  
Jan Paca ◽  
Eva Klapkova ◽  
Marie Stiborova ◽  
Carlos R Soccol ◽  
...  

Candida tropicalis can use phenol as the sole carbon and energy source. Experiments regarding phenol degradations from the water phase were carried out. The fermentor was operated as a fed-batch system with oxistat control. Under conditions of nutrient limitation and an excess of oxygen the respiration activity of cells was suppressed and some color metabolites (black-brown) started to be formed. An accumulation of these products inhibited the cell growth under aerobic conditions. Another impact was a decrease of the phenol hydroxylase activity as the key enzyme of the phenol degradation pathway at the end of the cell respiration activity. This decrease is linked with the above mentioned product inhibition. The cell death studied by fluorescent probe proceeded very slowly after the loss of the respiration activity. The starvation stress induced an increase of the endogenous respiration rate at the expense of phenol oxidation.


1989 ◽  
Vol 21 (4-5) ◽  
pp. 55-65 ◽  
Author(s):  
T. Kobayashi ◽  
T. Hashinaga ◽  
E. Mikami ◽  
T. Suzuki

Anaerobic phenol and benzoate degrading consortia were cultivated by acclimation of methanogenic sludges to be capable of degrading completely to CO2 and CH4 1,000 mg/l of phenol within 5–7 days, and 3,000 mg/l of benzoate within 5–7 days, respectively. By using the acclimated sludges, the effect of gaseous atmospheres (H2:CO2/80:20 and N2:CO2/80:20) on the biodegradability and the degradation pathways of phenol and benzoate were examined. Although the anaerobic degradation of phenol was accelerated in the H2/CO2 atmosphere compared with the N2/CO2 atmosphere, benzoate was accumulated. Degradations of benzoate and butyrate were inhibited in the H2/CO2 atmosphere under stirred conditions, but not under static conditions. Through a series of biodegradation tests by using several intermediates in phenol degradation reported previously, the anaerobic degradation pathway of phenol in the N2/CO2 atmosphere was suggested to be phenol → benzoate → cyclohexane carboxylate (or 1-cyclohexene carboxylate) → fatty acids → CO2,CH4.


Gene ◽  
1994 ◽  
Vol 151 (1-2) ◽  
pp. 29-36 ◽  
Author(s):  
Lee Ching Ng ◽  
Victoria Shingle ◽  
Chun Chau Sze ◽  
Chit Laa Poh

2021 ◽  
Vol 11 ◽  
Author(s):  
Jacqueline Wolf ◽  
Julia Koblitz ◽  
Andreas Albersmeier ◽  
Jörn Kalinowski ◽  
Bettina Siebers ◽  
...  

Present in many industrial effluents and as common degradation product of organic matter, phenol is a widespread compound which may cause serious environmental problems, due to its toxicity to animals and humans. Degradation of phenol from the environment by mesophilic bacteria has been studied extensively over the past decades, but only little is known about phenol biodegradation at high temperatures or low pH. In this work we studied phenol degradation in the thermoacidophilic archaeon Saccharolobus solfataricus P2 (basonym: Sulfolobus solfataricus) under extreme conditions (80°C, pH 3.5). We combined metabolomics and transcriptomics together with metabolic modeling to elucidate the organism’s response to growth with phenol as sole carbon source. Although S. solfataricus is able to utilize phenol for biomass production, the carbon source induces profound stress reactions, including genome rearrangement as well as a strong intracellular accumulation of polyamines. Furthermore, computational modeling revealed a 40% higher oxygen demand for substrate oxidation, compared to growth on glucose. However, only 16.5% of oxygen is used for oxidation of phenol to catechol, resulting in a less efficient integration of carbon into the biomass. Finally, our data underlines the importance of the phenol meta-degradation pathway in S. solfataricus and enables us to predict enzyme candidates involved in the degradation processes downstream of 2-hydroxymucconic acid.


2000 ◽  
Vol 66 (1) ◽  
pp. 163-169 ◽  
Author(s):  
Arlene A. Wise ◽  
Cheryl R. Kuske

ABSTRACT The genetic systems of bacteria that have the ability to use organic pollutants as carbon and energy sources can be adapted to create bacterial biosensors for the detection of industrial pollution. The creation of bacterial biosensors is hampered by a lack of information about the genetic systems that control production of bacterial enzymes that metabolize pollutants. We have attempted to overcome this problem through modification of DmpR, a regulatory protein for the phenol degradation pathway of Pseudomonassp. strain CF600. The phenol detection capacity of DmpR was altered by using mutagenic PCR targeted to the DmpR sensor domain. DmpR mutants were identified that both increased sensitivity to the phenolic effectors of wild-type DmpR and increased the range of molecules detected. The phenol detection characteristics of seven DmpR mutants were demonstrated through their ability to activate transcription of alacZ reporter gene. Effectors of the DmpR derivatives included phenol, 2-chlorophenol, 2,4-dichlorophenol, 4-chloro-3-methylphenol, 2,4-dimethylphenol, 2-nitrophenol, and 4-nitrophenol.


2004 ◽  
Vol 70 (4) ◽  
pp. 1907-1912 ◽  
Author(s):  
Grit Neumann ◽  
Riho Teras ◽  
Liis Monson ◽  
Maia Kivisaar ◽  
Frieder Schauer ◽  
...  

ABSTRACT The strain Pseudomonas sp. strain ADP is able to degrade atrazine as a sole nitrogen source and therefore needs a single source for both carbon and energy for growth. In addition to the typical C source for Pseudomonas, Na2-succinate, the strain can also grow with phenol as a carbon source. Phenol is oxidized to catechol by a multicomponent phenol hydroxylase. Catechol is degraded via the ortho pathway using catechol 1,2-dioxygenase. It was possible to stimulate the strain in order to degrade very high concentrations of phenol (1,000 mg/liter) and atrazine (150 mg/liter) simultaneously. With cyanuric acid, the major intermediate of atrazine degradation, as an N source, both the growth rate and the phenol degradation rate were similar to those measured with ammonia as an N source. With atrazine as an N source, the growth rate and the phenol degradation rate were reduced to ∼35% of those obtained for cyanuric acid. This presents clear evidence that although the first three enzymes of the atrazine degradation pathway are constitutively present, either these enzymes or the uptake of atrazine is the bottleneck that diminishes the growth rate of Pseudomonas sp. strain ADP with atrazine as an N source. Whereas atrazine and cyanuric acid showed no significant toxic effect on the cells, phenol reduces growth and activates or induces typical membrane-adaptive responses known for the genus Pseudomonas. Therefore Pseudomonas sp. strain ADP is an ideal bacterium for the investigation of the regulatory interactions among several catabolic genes and stress response mechanisms during the simultaneous degradation of toxic phenolic compounds and a xenobiotic N source such as atrazine.


2011 ◽  
Vol 183-185 ◽  
pp. 575-579
Author(s):  
Hui Wang ◽  
Zhao Yong Bian ◽  
Guang Lu ◽  
Xiang Jia Wei ◽  
Xiu Juan Yu ◽  
...  

Electrochemical degradation of phenol was studied in an undivided cell with a Ti/IrO2/RuO2 anode and a carbon/polytetrafluoroethylene (C/PTFE) O2-fed cathode which produced hydrogen peroxide (H2O2) by the electro-reduction of dissolved oxygen. The effect of current density, supporting electrolyte concentration and initial pH on the removal efficiency of phenol were investigated systematically. Results indicated that the optimal removal efficiency of phenol was achieved under the conditions of current density of 39 mA/cm2 and supporting electrolyte concentration of 0.02 mol/L. The phenol removal efficiency in the neutral condition was higher than that of acidic and basic conditions. The chemical oxygen demand (COD) and total organic carbon (TOC) removal achieved 71.6% and 63.6% for 100 min’s electrolysis, respectively. Benzoquinone, maleic acid, oxalic acid, acetic acid and formic acid were identified as intermediates by HPLC. A general phenol degradation pathway involving all these intermediates was proposed.


Sign in / Sign up

Export Citation Format

Share Document