Strain-dependent inhibition of nitrous oxide reduction in denitrifiers by yeast extract

1987 ◽  
Vol 33 (11) ◽  
pp. 1032-1037 ◽  
Author(s):  
Yiu-Kwok Chan ◽  
Peter R. Marshall

Pseudomonas sp. type strain H8 (ATCC 35402) was shown to be capable of denitrification but unable to reduce N2O in a complex medium containing 0.15% yeast extract. When added to a defined medium, autoclaved or filter-sterilized yeast extract from various suppliers was confirmed to inhibit N2O reduction by H8. The inhibition increased to 90% when the yeast extract concentration was increased to 0.5% in the medium. Only one of seven other denitrifying pseudomonads tested was similarly inhibited. Fractionation of yeast extract on a Sephadex G-10 column showed that the component responsible was a small molecule (molecular weight <700) that eluted with the first uv absorption peak. The inhibition was reversible by the addition of 10 μM Cu2+. Reduced glutathione was assayed in the first fraction of the Sephadex eluate and was found to mimic the effect of yeast extract. It is proposed that yeast extract inhibits N2O reduction by certain denitrifiers through glutathione complexing of Cu2+ which is a cofactor of N2O reductase.

Parasitology ◽  
1997 ◽  
Vol 115 (1) ◽  
pp. 81-89 ◽  
Author(s):  
N. GRANDE ◽  
E. PRECIGOUT ◽  
M. L. ANCELIN ◽  
K. MOUBRI ◽  
B. CARCY ◽  
...  

Babesia divergens was cultivated in RPMI 1640 (25 mM HEPES) supplemented with 10% human serum (RPMI-10% HS) with a high percentage of parasitized erythrocytes (PPE) ([ges ]40%). Standardization of in vitro tests, purification of exoantigens, biochemical studies and the safety of the culture handler motivated the development of a serum-free defined medium. Removal of serum greatly reduced the PPE but, after a period of adaptation, the culture was continuous and the parasite was able to develop a 3% routine PPE. Addition of vitamins or reduced glutathione in basal medium (RPMI) did not improve the PPE. The supplementation of basal medium with lipidic carrier (Albumax I or bovine serum albumin–Cohn's fraction V) promoted the growth of B. divergens with high PPE (>30%) close to those obtained in RPMI–10% HS. Neither protein nor lipid fractions alone were able to restore the growth of B. divergens. Nevertheless, the whole lipid fraction from serum or Albumax I added to delipidated albumin partially restored the growth (7% PPE), indicating that the presentation of specific lipids by a carrier is crucial for the parasite. All the data indicate that Albumax I can replace human serum offering the advantages of safety, standardization for chemosensitivity tests, and exoantigen purification.


2007 ◽  
Vol 4 (4) ◽  
pp. 622-627 ◽  
Author(s):  
Baghdad Science Journal

Thiamine stimulates the production of a red pigment , which is chromatographically and spectrophotometrically identical to prodigiosin , by growing cultures of serratia marcescens mutant 9-3-3 . this mutant is blocked in the formation of 2- methyl -3- amyl pyrorol( MAP),the monopyrrole moiety of prodigiosin , but accumulates 4-methoxy-2, 2-bipyrrole -5- carboxaldehyde (MBC) and can couple this compound with( MAP) to form prodigiosin . Addition of thiamine caused production of( MAP) , and as little as 0.02 mg of thiamine / ml in peptone- glycerol medium stimulated production of measurable amounts of prodigiosin. Phosphate saltes and another type of peptone decreased the thiamine- induced formation of prodigiosin ,yeast extract and glycerol enhanced formation of this substance. Thiamine also enhanced production of prodigiosin by wiled – type Strain Nima of S. marcescens . The pyrimidine moiety of thiamine was also 10% as effective as the vitamin ; the thiazol moiety only 4% , and the two moieties together , 25% . Thiamine did not stimulate production of prodigiosin biosynthesis as strain 9-3-3 . This is not surprising since strain 9-3-3 originated as a result of two mutational events one event may involve thiamine directly , and the other may involve the biosynthesis of( MAP).


2007 ◽  
Vol 72 (9) ◽  
pp. 1269-1283 ◽  
Author(s):  
Jiří Raška ◽  
František Skopal ◽  
Karel Komers ◽  
Jaroslav Machek

Biotransformation of glycerol to 1,3-dihydroxyacetone was carried out in an isothermal isochoric batch reactor with Gluconobacter oxydans immobilized in poly(vinyl alcohol) gel capsules. The reaction course was described with a three-step kinetic model. Two reaction schemes were proposed and compared with 8 kinetic experiments at 25 °C. The experimental dependences of glycerol and dihydroxyacetone concentrations on reaction time were simulated very well by the autocatalytic model. The effects of reaction temperature and initial concentrations of yeast extract and glycerol were studied. Temperature 25-30 °C, initial yeast extract concentration 2-4 g l-1 and initial glycerol concentration 20-50 g l-1 were found as optimal. The determined rate constants can be used to advantage for industrial production of dihydroxyacetone from glycerol.


1999 ◽  
Vol 65 (6) ◽  
pp. 2429-2438 ◽  
Author(s):  
Brion K. Duffy ◽  
Geneviève Défago

ABSTRACT Understanding the environmental factors that regulate the biosynthesis of antimicrobial compounds by disease-suppressive strains of Pseudomonas fluorescens is an essential step toward improving the level and reliability of their biocontrol activity. We used liquid culture assays to identify several minerals and carbon sources which had a differential influence on the production of the antibiotics 2,4-diacetylphloroglucinol (PHL), pyoluteorin (PLT), and pyrrolnitrin and the siderophores salicylic acid and pyochelin by the model strain CHA0, which was isolated from a natural disease-suppressive soil in Switzerland. Production of PHL was stimulated by Zn2+, NH4Mo2+, and glucose; the precursor compound mono-acetylphloroglucinol was stimulated by the same factors as PHL. Production of PLT was stimulated by Zn2+, Co2+, and glycerol but was repressed by glucose. Pyrrolnitrin production was increased by fructose, mannitol, and a mixture of Zn2+ and NH4Mo2+. Pyochelin production was increased by Co2+, fructose, mannitol, and glucose. Interestingly, production of its precursor salicylic acid was increased by different factors, i.e., NH4Mo2+, glycerol, and glucose. The mixture of Zn2+ and NH4Mo2+with fructose, mannitol, or glycerol further enhanced the production of PHL and PLT compared with either the minerals or the carbon sources used alone, but it did not improve siderophore production. Extending fermentation time from 2 to 5 days increased the accumulation of PLT, pyrrolnitrin, and pyochelin but not of PHL. When findings with CHA0 were extended to an ecologically and genetically diverse collection of 41 P. fluorescens biocontrol strains, the effect of certain factors was strain dependent, while others had a general effect. Stimulation of PHL by Zn2+ and glucose was strain dependent, whereas PLT production by all strains that can produce this compound was stimulated by Zn2+ and transiently repressed by glucose. Inorganic phosphate reduced PHL production by CHA0 and seven other strains tested but to various degrees. Production of PLT but not pyrrolnitrin by CHA0 was also reduced by 100 mM phosphate. The use of 1/10-strength nutrient broth-yeast extract, compared with standard nutrient broth-yeast extract, amended with glucose and/or glycerol resulted in dramatically increased accumulations of PHL (but not PLT), pyochelin, and salicylic acid, indicating that the ratio of carbon source to nutrient concentration played a key role in the metabolic flow. The results of this study (i) provide insight into the biosynthetic regulation of antimicrobial compounds, (ii) limit the number of factors for intensive study in situ, and (iii) indicate factors that can be manipulated to improve bacterial inoculants.


1986 ◽  
Vol 41 (1-2) ◽  
pp. 202-205 ◽  
Author(s):  
Otto Holst ◽  
Jürgen Weckesser ◽  
Baldur Rieth ◽  
Crawford S. Dow

Abstract The compositions of lipopolysaccharides from the photoheterotrophic budding Rhodomi­crobium vannielii strains DSM 162, Rm5, E3 and 2/1 are reported. Common constituents of these lipopolysaccharides are glucose, mannose, glucosamine, glucuronic and galacturonic acids, 2-keto-3-deoxyoctonate (KDO) and the fatty acids 3-OH-C16:0, 3-OH-C14:0, C14:0, Δ14-C22:1, aside from strain specific differences. Two different, medium-dependent growth forms of strain DSM 162 are described. The vitamin/ yeast extract-concentration in the medium and/or the growth temperature were found as factors triggering the different growth forms. Lipopolysaccharides of the two growth forms had only quantitative differences in composition. Lipopolysaccharide from swarmer cells of strain Rm5 showed a chemical composition comparable to that of chain cells and from simple cycle cells of the same strain.


1998 ◽  
Vol 38 (1) ◽  
pp. 237-246 ◽  
Author(s):  
Barbara Schönharting ◽  
Ruxandra Rehner ◽  
Jörg W. Metzger ◽  
Karlheinz Krauth ◽  
Manfred Rizzi

A new mathematical model is presented which describes the denitrification process by dynamic material balance equations. In this approach the kinetic rate expressions of the single denitrification steps and the observed strong inhibition of nitrate on nitrite and nitrous oxide reduction are based exclusively on fundamental enzyme kinetics. This allows a prediction of the denitrification process in a wide range of wastewater-relevant nitrate concentrations. The model was successfully applied to the description of the kinetic behavior of a standardized denitrifying activated sludge system. Furthermore the experimentally investigated influence of hydrogen sulfide was quantified by extending the model with a non-competitive inhibition mechanism involving all steps of the denitrification process. The inhibitory effect was related to the free membrane-permeable hydrogen sulfide concentration. This means that the extent of its inhibition depends additionally on the pH-value. Even very low hydrogen sulfide concentrations lead to a strong inhibition of nitrous oxide reduction and therefore to a high release of nitrous oxide from wastewater treatment plants.


2018 ◽  
Vol 37 (1) ◽  
pp. 2-6 ◽  
Author(s):  
Michaela J. Schultz ◽  
John H. Connor ◽  
Horacio M. Frydman

2007 ◽  
Vol 57 (11) ◽  
pp. 2557-2561 ◽  
Author(s):  
Takashi Itoh ◽  
Naoto Yoshikawa ◽  
Tomonori Takashina

A novel thermoacidophilic, cell wall-less archaeon, strain IC-189T, was isolated from a solfataric field in Ohwaku-dani, Hakone, Japan. The cells were irregular cocci, sometimes lobed, club-shaped or catenated, and were highly variable in size, ranging from 0.8 to 8.0 μm in diameter. The strain grew at temperatures in the range 38–68 °C (optimally at 60 °C) and at pH 1.8–4.0 (optimally at around pH 3.0). Strain IC-189T was obligately aerobic and heterotrophic, requiring yeast extract for growth. Yeast extract, glucose and mannose served as carbon and energy sources. The polar lipids consisted mainly of cyclic or acyclic glycerol-bisdiphytanyl-glycerol tetraethers, and the predominant quinone was a menaquinone with seven isoprenoid units (MK-7). The G+C content of total DNA was 56.1 mol%. 16S rRNA gene sequence analysis revealed that strain IC-189T was a member of the order Thermoplasmatales, but diverged from the hitherto known species of the genera Thermoplasma, Picrophilus and Ferroplasma (86.2–91.0 % sequence similarity). These phenotypic and phylogenetic properties clearly support a separate taxonomic status for this strain. Therefore, strain IC-189T represents a novel genus (order Thermoplasmatales) and species, for which the name Thermogymnomonas acidicola gen. nov., sp. nov. is proposed, with type strain IC-189T (=JCM 13583T=DSM 18835T).


Sign in / Sign up

Export Citation Format

Share Document