Production of metabolites from chlorobiphenyls by resting cells ofPseudomonasstrain LB400 after growth on different carbon sources

1999 ◽  
Vol 45 (2) ◽  
pp. 178-184 ◽  
Author(s):  
K A Billingsley ◽  
S M Backus ◽  
O P Ward
Keyword(s):  
Carbon Source ◽  
Polychlorinated Biphenyl ◽  
Carbon Sources ◽  
Resting Cells ◽  
Metabolite Formation ◽  
Chlorobenzoic Acid ◽  
Metabolite Production ◽  
Pcb Congeners ◽  
Chlorobenzoic Acids ◽  
General Order

Cells of Pseudomonas strain LB400, grown on biphenyl, glucose, or glycerol, transformed polychlorinated biphenyl (PCB) congeners into chlorobenzoic acid (CBA) metabolites. Transformation of the PCB congeners, 2,3-chlorobiphenyl (CBP), 2,2'-CBP, 2,5,4'-CBP, and 2,4,2',4'-CBP, produced the metabolites, 2,3-CBA, 2-CBA, 4-CBA, and 2,4-CBA, respectively. Rates and extents of PCB transformation and metabolite formation were highest with biphenyl-grown cells. Intermediate rates of metabolite production were observed with glycerol-grown cells, and lowest rates of production were found with glucose-grown cells. Regardless of carbon source, the rate of degradation of congeners was faster than the rate of production of CBAs. Relative rates of PCB transformation and metabolite production from different congeners with cells grown on a particular substrate followed the same general order, 2,3-CBA (from 2,3-CBP) > 2-CBA (from 2,2'-CBP) > 4-CBA (from 2,5,4'-CBP) > 2,4-CBA (from 2,4,2',4'-CBP). Pseudomonas strain LB400 appeared unable to grow on any of the chlorobenzoic acids. However, Pseudomonas strain LB400 cells grown on biphenyl appeared capable of degrading 2-CBA and 2,3-CBA but not 4-CBA nor 2,4-CBA. Cells grown on glycerol appeared unable to metabolize any CBAs.Key words: polychlorinated biphenyls, metabolites, Pseudomonas LB400.

Studies on the transformation of selected polychlorinated biphenyl congeners by Pseudomonas strain LB 400

1997 ◽  
Vol 43 (8) ◽  
pp. 782-788 ◽  
Author(s):  
K. A. Billingsley ◽  
O. P. Ward ◽  
S. M. Backus
Keyword(s):  
Carbon Source ◽  
Polychlorinated Biphenyls ◽  
Incubation Period ◽  
Polychlorinated Biphenyl ◽  
Carbon Sources ◽  
Lag Phase ◽  
Resting Cells ◽  
Major Objective ◽  
Pcb Congeners ◽  
Degradation Medium

Resting cells of Pseudomonas strain LB400 are known to transform polychlorinated biphenyls (PCBs) when the cells are previously grown on biphenyl. In this study, PCB transformation was also observed in resting cells grown on other substrates such as glucose and glycerol. The presence of PCB congeners in the growth medium increased the lag phase for the growth of cells on a biphenyl substrate but not on a glycerol substrate. Supplementation of the degradation medium with biphenyl dramatically decreased the rate of PCB congener transformation, while the presence of glycerol or glucose had little or no effect on PCB transformation rates. Removal rates with biphenyl-grown cells in the standard degradation medium for 2,4,2′,4′-tetrachlorobiphenyl, 2,4,5,2′,5′-pentachlorobiphenyl, and 2,3-dichlorobiphenyl were 1.06, 1.66, and 224 μmol/(L∙h), respectively. Relative rates of transformation of 2,3-dichlorobiphenyl by biphenyl-, glucose-, and glycerol-grown cells were 100:36:36 and were similar to the relative rates of transformation of 2,4,5,2′,5′-pentachlorobiphenyl (100:33:42). The presence of PCBs adversely affected cell viability of biphenyl-grown cells over a 48-h incubation period and may explain the decline observed in PCB conversion capacity over the same incubation period. A major objective of this study was to investigate the significance of using biphenyl as the carbon source for growth of Pseudomonas strain LB400 cells capable of PCB transformation. Our findings indicate that, whereas higher rates of transformation of PCBs are observed with biphenyl-grown cells, cells grown on other carbon sources retain PCB-transforming enzymes. In addition, it has been demonstrated that biphenyl inhibits transformation of PCBs by the organism, whereas glycerol or glucose does not.Key words: Pseudomonas strain LB400, polychlorinated biphenyls, degradation, biphenyl.

scholarly journals Pyruvate accelerates palladium reduction by regulating catabolism and electron transfer pathway in Shewanella oneidensis

2021 ◽  
Author(s):  
Yuan-Yuan Cheng ◽  
Wen-Jing Wang ◽  
Shi-Ting Ding ◽  
Ming-Xing Zhang ◽  
Ai-Guo Tang ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Carbon Source ◽  
Time Window ◽  
Carbon Sources ◽  
Shewanella Oneidensis ◽  
Underlying Mechanism ◽  
Extracellular Electron Transfer ◽  
Resting Cells ◽  
Electron Transfer Pathway ◽  
Specific Regulation

Shewanella oneidensis is a model strain of the electrochemical active bacteria (EAB) because of its strong capability of extracellular electron transfer (EET) and genetic tractability. In this study, we investigated the effect of carbon sources on EET in S. oneidensis by using reduction of palladium ions (Pd(II)) as a model and found that pyruvate greatly accelerated the Pd(II) reduction compared with lactate by resting cells. Both Mtr pathway and hydrogenases played a role in Pd(II) reduction when pyruvate was used as a carbon source. Furthermore, in comparison with lactate-feeding S. oneidensis, the transcriptional levels of formate dehydrogenases involving in pyruvate catabolism, Mtr pathway, and hydrogenases in pyruvate-feeding S. oneidensis were up-regulated. Mechanistically, the enhancement of electron generation from pyruvate catabolism and electron transfer to Pd(II) explains the pyruvate effect on Pd(II) reduction. Interestingly, a 2-h time window is required for pyruvate to regulate transcription of these genes and profoundly improve Pd(II) reduction capability, suggesting a hierarchical regulation for pyruvate sensing and response in S. oneidensis. IMPORTANCE The unique respiration of EET is crucial for the biogeochemical cycling of metal elements and diverse applications of EAB. Although a carbon source is a determinant factor of bacterial metabolism, the research into the regulation of carbon source on EET is rare. In this work, we reported the pyruvate-specific regulation and improvement of EET in S. oneidensis and revealed the underlying mechanism, which suggests potential targets to engineer and improve the EET efficiency of this bacterium. This study sheds light on the regulatory role of carbon sources in anaerobic respiration in EAB, providing a way to regulate EET for diverse applications from a novel perspective.

Comparison of the degradation patterns of polychlorinated biphenyl congeners in Aroclors byPseudomonasstrain LB400 after growth on various carbon sources

1997 ◽  
Vol 43 (12) ◽  
pp. 1172-1179 ◽  
Author(s):  
K. A. Billingsley ◽  
C. Juneson ◽  
O. P. Ward ◽  
S. M. Backus
Keyword(s):  
Polychlorinated Biphenyls ◽  
Rate Constants ◽  
Polychlorinated Biphenyl ◽  
Carbon Sources ◽  
Transformation Rate ◽  
Resting Cells ◽  
Growth Substrate ◽  
Aroclor 1242 ◽  
Time Courses

Resting cells of Pseudomonas strain LB400, grown on biphenyl, transformed 80, 50, and 17% of Aroclor 1242, 1254, and 1260, respectively. Resting cells grown on glucose or glycerol also transformed these polychlorinated biphenyl (PCB) mixtures to the extent of 60, 35, and 9% for Aroclors 1242, 1254, and 1260, respectively. Time courses of the transformation of the separated individual congeners in the Aroclors were plotted and used to determine the transformation rate constants (k). By analysis of the rate constants, it was concluded that the order of degradation of the different congeners in an Aroclor were similar regardless of the growth substrate. In general, k values for the conversion of a particular congener were lower for cells grown on glucose or glycerol compared with cells grown on biphenyl. Generally, k values for the transformation of the same congener in different Aroclors were not the same: rate constants had highest values for the congener in Aroclor 1242 and lowest values in Aroclor 1260. The data allowed congeners to be grouped according to their relative rates of degradation. The ratio of k values for transformation of individual congeners in Aroclors by cells grown on biphenyl and glucose were not constant.Key words: Pseudomonas strain LB400, polychlorinated biphenyls, Aroclors, transformation, resting cells.

Polychlorinated biphenyl induced hepatocyte alterations

1987 ◽  
Vol 45 ◽  
pp. 716-717
Author(s):  
D.N. Collins ◽  
J.N. Turner ◽  
K.O. Brosch ◽  
R.F. Seegal
Keyword(s):  
Lipid Droplets ◽  
Wistar Rats ◽  
Homovanillic Acid ◽  
Polychlorinated Biphenyl ◽  
Corn Oil ◽  
Environmental Pollutants ◽  
Short Term ◽  
Pcb Congeners ◽  
Urinary Levels ◽  
The Brain

Polychlorinated biphenyls (PCBs) are a ubiquitous class of environmental pollutants with toxic and hepatocellular effects, including accumulation of fat, proliferated smooth endoplasmic recticulum (SER), and concentric membrane arrays (CMAs) (1-3). The CMAs appear to be a membrane storage and degeneration organelle composed of a large number of concentric membrane layers usually surrounding one or more lipid droplets often with internalized membrane fragments (3). The present study documents liver alteration after a short term single dose exposure to PCBs with high chlorine content, and correlates them with reported animal weights and central nervous system (CNS) measures. In the brain PCB congeners were concentrated in particular regions (4) while catecholamine concentrations were decreased (4-6). Urinary levels of homovanillic acid a dopamine metabolite were evaluated (7).Wistar rats were gavaged with corn oil (6 controls), or with a 1:1 mixture of Aroclor 1254 and 1260 in corn oil at 500 or 1000 mg total PCB/kg (6 at each level).

Effect of carbon source on Phenobarbital metabolism by Rhizopus stolonifer

2010 ◽  
Vol 3 (2) ◽  
pp. 1022-1027
Author(s):  
Kavitha K ◽  
Asha S ◽  
Hima Bindu T.V.L ◽  
Vidyavathi M
Keyword(s):  
Carbon Source ◽  
High Performance ◽  
Carbon Sources ◽  
In Vitro Models ◽  
Rhizopus Stolonifer ◽  
Safety And Efficacy ◽  
Alternative Systems ◽  
Toxicological Studies ◽  
Microbial Model

The safety and efficacy of a drug is based on its metabolism or metabolite formed. The metabolism of drugs can be studied by different in vitro models, among which microbial model became popular. In the present study, eight microbes were screened for their ability to metabolize phenobarbital in a manner comparable to humans with a model to develop alternative systems to study human drug metabolism. Among the different microbes screened, a filamentous fungi Rhizopus stolonifer metabolized phenobarbital to its metabolite which is used for further pharmacological and toxicological studies. The transformation of phenobarbital was identified by high- performance liquid chromatography (HPLC). Interestingly, Rhizopus stolonifer sample showed an extra metabolite peak at 3.11min. compared to its controls. The influence of different carbon sources in media used for growth of fungus, on metabolite production was studied, to find its effect in production of metabolite as the carbon source may influence the growth of the cell.

scholarly journals Denitrification Control in a Recirculating Aquaculture System—A Simulation Study

Processes ◽  
2020 ◽  
Vol 8 (10) ◽  
pp. 1306
Author(s):  
Pedro Almeida ◽  
Laurent Dewasme ◽  
Alain Vande Wouwer
Keyword(s):  
Carbon Source ◽  
Carbon Sources ◽  
Aquatic Organisms ◽  
Operating Conditions ◽  
Toxic Substances ◽  
Recirculating Aquaculture System ◽  
Treatment Technology ◽  
Tuning Method ◽  
Recirculating Aquaculture ◽  
Aquaculture System

The recirculating aquaculture system (RAS) is a land-based water treatment technology, which allows for farming aquatic organisms, such as fish, by reusing the water in the production (often less than 5%). This technology is based on the use of filters, either mechanical or biological, and can, in principle, be used for any species grown in aquaculture. Due to the low recirculation rate, ammonia accumulates in the system and must be converted into nitrate using nitrification reactors. Although less toxic for fish, nitrate can also be further reduced into nitrogen gas by the use of denitrification biofilters which may create several issues, such as incomplete denitrification, resulting in toxic substances, such as nitrite and nitric oxide, or a waste of carbon source in excess. Control of the added quantity of carbon source in the denitrification biofilter is then mandatory to keep nitrate/nitrite concentrations under toxic levels for fish and in accordance with local effluent regulations, and to reduce costs related to wasted organic carbon sources. This study therefore investigates the application of different control methodologies to a denitrification reactor in a RAS. To this end, a numerical simulator is built to predict the RAS behavior and to allow for the comparison of different control approaches, in the presence of changes in the operating conditions, such as fish density and biofilter removal efficiency. First, a classical proportional-integral-derivative (PID) controller was designed, based on an SIMC tuning method depending on the amount of ammonia excreted by fish. Then, linearizing and cascade controllers were considered as possible alternatives.

scholarly journals The carbon source-dependent pattern of antimicrobial activity and gene expression in Pseudomonas donghuensis P482

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Marta Matuszewska ◽  
Tomasz Maciąg ◽  
Magdalena Rajewska ◽  
Aldona Wierzbicka ◽  
Sylwia Jafra
Keyword(s):  
Gene Expression ◽  
Antimicrobial Activity ◽  
Carbon Source ◽  
Reference Genes ◽  
Plant Pathogens ◽  
Plant Protection ◽  
Carbon Sources ◽  
Unknown Compound ◽  
Fungal Plant Pathogens ◽  
The Impact

AbstractPseudomonas donghuensis P482 is a tomato rhizosphere isolate with the ability to inhibit growth of bacterial and fungal plant pathogens. Herein, we analysed the impact of the carbon source on the antibacterial activity of P482 and expression of the selected genes of three genomic regions in the P482 genome. These regions are involved in the synthesis of pyoverdine, 7-hydroxytropolone (7-HT) and an unknown compound (“cluster 17”) and are responsible for the antimicrobial activity of P482. We showed that the P482 mutants, defective in these regions, show variations and contrasting patterns of growth inhibition of the target pathogen under given nutritional conditions (with glucose or glycerol as a carbon source). We also selected and validated the reference genes for gene expression studies in P. donghuensis P482. Amongst ten candidate genes, we found gyrB, rpoD and mrdA the most stably expressed. Using selected reference genes in RT-qPCR, we assessed the expression of the genes of interest under minimal medium conditions with glucose or glycerol as carbon sources. Glycerol was shown to negatively affect the expression of genes necessary for 7-HT synthesis. The significance of this finding in the light of the role of nutrient (carbon) availability in biological plant protection is discussed.

Development of mutants of Gliocladium virens tolerant to benomyl

1990 ◽  
Vol 36 (7) ◽  
pp. 484-489 ◽  
Author(s):  
G. C. Papavizas ◽  
D. P. Roberts ◽  
K. K. Kim
Keyword(s):  
Carbon Source ◽  
Type Strain ◽  
Wild Type Strain ◽  
Carbon Sources ◽  
Sclerotium Rolfsii ◽  
Wild Type ◽  
Gliocladium Virens ◽  
Rhizosphere Competence ◽  
Filter Paper Cellulase ◽  
Type Strains

Aqueous suspensions of conidia of Gliocladium virens strains Gl-3 and Gl-21 were exposed to both ultraviolet radiation and ethyl methanesulfonate. Two mutants of Gl-3 and three of Gl-21 were selected for tolerance to benomyl at 10 μg∙mL−1, as indicated by growth and conidial germination on benomyl-amended potato dextrose agar. The mutants differed considerably from their respective wild-type strains in appearance, growth habit, sporulation, carbon-source utilization, and enzyme activity profiles. Of 10 carbon sources tested, cellobiose, xylose, and xylan were the best for growth, galactose and glucose were intermediate, and arabinose, ribose, and rhamnose were poor sources of carbon. The wild-type strains and the mutants did not utilize cellulose as the sole carbon source for growth. Two benomyl-tolerant mutants of Gl-3 produced less cellulase (β-1,4-glucosidase, carboxymethylcellulase, filter-paper cellulase) than Gl-3. In contrast, mutants of Gl-21 produced more cellulase than the wild-type strain. Only Gl-3 provided control of blight on snapbean caused by Sclerotium rolfsii. Wild-type strain Gl-21 and all mutants from both strains were ineffective biocontrol agents. Key words: Gliocladium, benomyl tolerance, Sclerotium, rhizosphere competence.

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