Continuous cultures for alginate production by Azotobacter vinelandii growing at different oxygen uptake rates

2011 ◽  
Vol 46 (9) ◽  
pp. 1879-1883 ◽  
Author(s):  
Alvaro Díaz-Barrera ◽  
Alberto Aguirre ◽  
Julio Berrios ◽  
Fernando Acevedo
Keyword(s):  
Oxygen Uptake ◽  
Azotobacter Vinelandii ◽  
Continuous Cultures ◽  
Alginate Production ◽  
Uptake Rates

THE METABOLISM OF NORMAL BRAIN AND HUMAN GLIOMAS IN RELATION TO CELL TYPE AND DENSITY

1955 ◽  
Vol 33 (3) ◽  
pp. 395-403 ◽  
Author(s):  
Irving H. Heller ◽  
K. A. C. Elliott
Keyword(s):  
Cerebral Cortex ◽  
White Matter ◽  
Brain Tumors ◽  
Corpus Callosum ◽  
Oxygen Uptake ◽  
Glial Cells ◽  
Cerebellar Cortex ◽  
Unit Weight ◽  
Uptake Rates ◽  
The Brain

Per unit weight, cerebral and cerebellar cortex respire much more actively than corpus callosum. The rate per cell nucleus is highest in cerebral cortex, lower in corpus callosum, and still lower in cerebellar cortex. The oxygen uptake rates of the brain tumors studied, with the exception of an oligodendroglioma, were about the same as that of white matter on the weight basis but lower than that of cerebral cortex or white matter on the cell basis. In agreement with previous work, an oligodendroglioma respired much more actively than the other tumors. The rates of glycolysis of the brain tumors per unit weight were low but, relative to their respiration rate, glycolysis was higher than in normal gray or white matter. Consideration of the figures obtained leads to the following tentative conclusions: Glial cells of corpus callosum respire more actively than the neurons of the cerebellar cortex. Neurons of the cerebral cortex respire on the average much more actively than neurons of the cerebellar cortex or glial cells. Considerably more than 70% of the oxygen uptake by cerebral cortex is due to neurons. The oxygen uptake rates of normal oligodendroglia and astrocytes are probably about the same as the rates found per nucleus in an oligodendroglioma and in astrocytomas; oligodendroglia respire much more actively than astrocytes.

scholarly journals The algT Gene of Pseudomonas syringae pv. glycinea andNew Insights into the Transcriptional Organization of thealgT-muc Gene Cluster

2006 ◽  
Vol 188 (23) ◽  
pp. 8013-8021 ◽  
Author(s):  
Alexander Schenk ◽  
Michael Berger ◽  
Lisa M. Keith ◽  
Carol L. Bender ◽  
Georgi Muskhelishvili ◽  
...  
Keyword(s):  
Gene Cluster ◽  
Pseudomonas Syringae ◽  
Azotobacter Vinelandii ◽  
Regulatory Gene ◽  
In Planta ◽  
Phytopathogenic Bacterium ◽  
Reverse Transcription Pcr ◽  
Alginate Production ◽  
Alginate Biosynthesis

ABSTRACT The phytopathogenic bacterium Pseudomonas syringae pv. glycinea infects soybean plants and causes bacterial blight. In addition to P. syringae, the human pathogen Pseudomonas aeruginosa and the soil bacterium Azotobacter vinelandii produce the exopolysaccharide alginate, a copolymer of d-mannuronic and l-guluronic acids. Alginate production in P. syringae has been associated with increased fitness and virulence in planta. Alginate biosynthesis is tightly controlled by proteins encoded by the algT-muc regulatory gene cluster in P. aeruginosa and A. vinelandii. These genes encode the alternative sigma factor AlgT (σ22), its anti-sigma factors MucA and MucB, MucC, a protein with a controversial function that is absent in P. syringae, and MucD, a periplasmic serine protease and homolog of HtrA in Escherichia coli. We compared an alginate-deficient algT mutant of P. syringae pv. glycinea with an alginate-producing derivative in which algT is intact. The alginate-producing derivative grew significantly slower in vitro growth but showed increased epiphytic fitness and better symptom development in planta. Evaluation of expression levels for algT, mucA, mucB, mucD, and algD, which encodes an alginate biosynthesis gene, showed that mucD transcription is not dependent on AlgT in P. syringae in vitro. Promoter mapping using primer extension experiments confirmed this finding. Results of reverse transcription-PCR demonstrated that algT, mucA, and mucB are cotranscribed as an operon in P. syringae. Northern blot analysis revealed that mucD was expressed as a 1.75-kb monocistronic mRNA in P. syringae.

Alginate production by Azotobacter vinelandii DSM576 in batch fermentation

1998 ◽  
Vol 20 (3-4) ◽  
pp. 171-176 ◽  
Author(s):  
E Parente ◽  
M A Crudele ◽  
M Aquino ◽  
F Clementi
Keyword(s):  
Batch Fermentation ◽  
Azotobacter Vinelandii ◽  
Alginate Production

scholarly journals Cultivation at high osmotic pressure confers ubiquinone 8–independent protection of respiration on Escherichia coli

2019 ◽  
Vol 295 (4) ◽  
pp. 981-993 ◽  
Author(s):  
Laura Tempelhagen ◽  
Anita Ayer ◽  
Doreen E. Culham ◽  
Roland Stocker ◽  
Janet M. Wood
Keyword(s):  
Oxidative Stress ◽  
Gene Expression ◽  
Escherichia Coli ◽  
Electron Transfer ◽  
Oxygen Uptake ◽  
Osmotic Pressure ◽  
Respiratory Chain ◽  
Membrane Lipid ◽  
E Coli ◽  
Uptake Rates

Ubiquinone 8 (coenzyme Q8 or Q8) mediates electron transfer within the aerobic respiratory chain, mitigates oxidative stress, and contributes to gene expression in Escherichia coli. In addition, Q8 was proposed to confer bacterial osmotolerance by accumulating during growth at high osmotic pressure and altering membrane stability. The osmolyte trehalose and membrane lipid cardiolipin accumulate in E. coli cells cultivated at high osmotic pressure. Here, Q8 deficiency impaired E. coli growth at low osmotic pressure and rendered growth osmotically sensitive. The Q8 deficiency impeded cellular O2 uptake and also inhibited the activities of two proton symporters, the osmosensing transporter ProP and the lactose transporter LacY. Q8 supplementation decreased membrane fluidity in liposomes, but did not affect ProP activity in proteoliposomes, which is respiration-independent. Liposomes and proteoliposomes prepared with E. coli lipids were used for these experiments. Similar oxygen uptake rates were observed for bacteria cultivated at low and high osmotic pressures. In contrast, respiration was dramatically inhibited when bacteria grown at the same low osmotic pressure were shifted to high osmotic pressure. Thus, respiration was restored during prolonged growth of E. coli at high osmotic pressure. Of note, bacteria cultivated at low and high osmotic pressures had similar Q8 concentrations. The protection of respiration was neither diminished by cardiolipin deficiency nor conferred by trehalose overproduction during growth at low osmotic pressure, but rather might be achieved by Q8-independent respiratory chain remodeling. We conclude that osmotolerance is conferred through Q8-independent protection of respiration, not by altering physical properties of the membrane.

Engineering aspects of a mixed methanotrophic culture in a membrane-aerated biofilm reactor

2004 ◽  
Vol 49 (11-12) ◽  
pp. 255-262 ◽  
Author(s):  
E. Casey ◽  
S. Rishell ◽  
B. Glennon ◽  
G. Hamer
Keyword(s):  
Oxygen Uptake ◽  
Biofilm Reactor ◽  
Specific Rate ◽  
Suspended Cell ◽  
Biofilm Thickness ◽  
Biofilm Reactors ◽  
Uptake Rates ◽  
Methane Uptake ◽  
Cell Processes ◽  
Oxidation Efficiency

Methanotrophic biodegradation using the membrane-aerated biofilm reactor (MABR) is a technology offering several advantages over both conventional biofilm reactors and suspended-cell processes. In this study the oxidation efficiency of a methanotrophic biofilm in a 1.5 litre MABR was investigated. Measurements of oxygen and methane uptake rates together with biofilm thickness were taken for developing biofilms. It was found that the specific rate of metabolic activity of the biofilm was unusually high as determined by the methane and oxygen uptake rates. Microbial activity stratification was evident and the location of stratified layers of oxygen consuming components of the consortium could be manipulated via the intra-membrane oxygen pressure.

Fixed Biomass Activity in Aerobic Biological Reactors Used for Wastewater Treatment

1988 ◽  
Vol 20 (11-12) ◽  
pp. 489-491
Author(s):  
J. C. Block ◽  
N. Nouvion ◽  
J. M. Cahen ◽  
Y. Lesty ◽  
G. M. Faup
Keyword(s):  
Wastewater Treatment ◽  
Oxygen Uptake ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Biomass Growth ◽  
Head Losses ◽  
Uptake Rates ◽  
Biomass Activity ◽  
Potential Activity ◽  
Experimental Runs

Experimental runs were carried out on an upflow fixed-bed reactor. The process cycle of 24 hours was determined by following head losses used as an indicator of the clogging of the filter and of the biomass growth. Thanks to a protocol of dispersion of the biomass present into the filter, two fractions defined as fixed and shared biomass were obtained. The specific dehydrogenase activities or the specific oxygen uptake rates of the dispersed biomass were always greater than those of the fixed biomass. The aggregation of the biomass into the reactor prevents its potential activity being used to the full.

scholarly journals Estimating the impact of inhibitory substances on activated sludge denitrification process

2019 ◽  
Vol 14 (4) ◽  
pp. 863-871 ◽  
Author(s):  
Kati Klein ◽  
Taavo Tenno
Keyword(s):  
Standard Deviation ◽  
Oxygen Uptake ◽  
Activated Sludge ◽  
Process Efficiency ◽  
Sludge Treatment ◽  
Conventional Activated Sludge ◽  
Uptake Rates ◽  
Relative Standard ◽  
The Impact ◽  
Denitrification Process

Abstract Industrial wastewater frequently contains substances which inhibit activated sludge treatment processes. Inhibitory characteristics of different substances are usually evaluated based on testing the impact of respective substance on activated sludge nitrification or oxygen uptake rates. However, denitrification is always before aerobic processes in conventional activated sludge treatment plants and thereby more exposed to inhibitory compounds. There is no easily applicable and validated method available for determination of denitrification process efficiency and inhibition. In this study, a method for evaluation of inhibition on the activated sludge denitrification process was developed and validated using 3,5-dichlorophenol (3,5-DCP) as a model inhibitory compound and additionally controlled with real wastewater produced in the shale oil industry. Average IC50 value (5.5 ± 2.2 mg L−1) for 3,5-DCP showed that denitrifiers were less sensitive than nitrifiers (IC50 = 2.9 ± 0.7 mg L−1) and more sensitive than aerobic heterotrophs (IC50 = 7.2 ± 2.4 mg L−1). Methodological aspects like accumulation of nitrite nitrogen, acclimatization of biomass and technical issues were discussed. Achieved validation characteristics were similar with ISO Standards estimating activated sludge nitrification and oxygen uptake rates, which proves the reliability of the method: standard deviation, 95.4% confidence level, relative standard deviation were calculated to be 2.2 mg L−1, 1.2 … 9.8 mg L−1 and 39.2%, respectively.

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