Abstract:
The invention concerns a novel isolated microorganism characterized in that it is capable of: i) transforming Kjeldahl nitrogen, ammonia nitrogen and/or nitrogen oxides into gas nitrogen; and ii) transforming carbonaceous matter into carbon dioxide; both transformation processes being carried out in aerobic condition. The invention also concerns a method for treating wastewater using said microorganism.
Abstract:
Novel strains of isolated and purified bacteria have been identified which have the ability to degrade petroleum hydrocarbons including a variety of PAHs. Several isolates also exhibit the ability to produce a biosurfactant. The combination of the biosurfactant-producing ability along with the ability to degrade PAHs enhances the efficiency with which PAHs may be degraded. Additionally, the biosurfactant also provides an additional ability to bind heavy metal ions for removal from a soil or aquatic environment.
Abstract:
The invention concerns a novel isolated microorganism characterized in that it is capable of: i) transforming Kjeldahl nitrogen, ammonia nitrogen and/or nitrogen oxides into gas nitrogen; and ii) transforming carbonaceous matter into carbon dioxide; both transformation processes being carried out in aerobic condition. The invention also concerns a method for treating wastewater using said microorganism.
Abstract:
Water-soluble ethers used as octane number enhancers in gasoline are disturbing components in soils and groundwater even in small amounts due to their strong taste and odour. This invention relates to biological purification of gasoline-contaminated soils and groundwater, more specifically to Variovorax strains being able to degrade ethers and their degradation products and to a mixed bacterial population comprising said bacteria. Further this invention relates to a process for bacterial degradation of ethers and their degradation products and to the use of one or more Variovorax strains of the invention in purifying contaminated soil or water.
Abstract:
A bacteria strain FERMBP-7046 belonging to the genus Acinetobacter, a strain FERMBP-7049 belonging to the genus Acinetobacter, a strain FERMBP-7047 belonging to the genus Pseudomonas, and a strain FERMBP-7048 belonging to the genus Alcaligenes are caused to act on an object of treatment, either individually or in a bacteria mixture including at least one of the foregoing strains. Thus it is possible to provide heavy oil degrading bacteria and a heavy oil degrading bacteria mixture which are inexpensively prepared, which simplify degradation and removal operations, and which can be stored and shipped simply, and to provide a nurturing composition for such bacteria, a method of degrading heavy oil using such bacteria, and building and civil engineering materials containing a substance obtained by heavy oil degradation treatment.
Abstract:
The microbiological process for the production of hydroxy-heterocyclic carboxylic acid of formula ##STR1## wherein R.sub.1 means a hydrogen or a halogen atom and X means a nitrogen atom or a CR.sub.2 function, wherein R.sub.2 means a hydrogen or halogen atom, starting from the corresponding heterocyclic carboxylic acid. The process is performed so that an aerobic biomass which utilizes nicotinic acid, is cultivated in a molar ratio of nicotinic acid to mineral acid of 1 to 8. The ratio is assured over the entire cultivation phase. The the hydroxylation of the corresponding heterocyclic carboxylic acid of the general formula ##STR2## wherein R.sub.1 and X have the above-mentioned meanings, is performed with the biomass. Under these conditions, strain Pseudomonas acidovorans DSM 7205, strain Pseudomonas acidovorans DSM 7203, strain Alcaligenes faecalis DSM 7204 and strain Arthrobacter crystallopoietes DSM 7202 are concentrated in the cultivation phase.
Abstract:
A method of assaying for acyl-L-carnitines including short chain acyl-carnitines including acetyl-L-carnitine and propionyl-L-carnitine in a substance, comprises subjecting a sample of the substance to be analyzed to an enzymatic hydrolysis using an acyl-carnitine esterase. The esterase is produced by Alcaligenes sp. FERM BP-2570 and it has substrate specificity for acyl-L-carnitines including short-chain acyl-L-carnitines. In addition the esterase demonstrates substrate specificity for acetyl-L-carnitine and propionyl-L-carnitine. The enzyme facilitates the hydrolysis reaction of one mole each of the acyl-L-carnitines with one mole of water in which to form one mole each of the corresponding fatty acid and L-carnitine. The amount of the fatty acid and L-carnitine formed is determined by this method.
Abstract translation:一种在物质中测定包括乙酰基-L-肉碱和丙酰基-L-肉碱的短链酰基肉碱的酰基-L-肉碱的方法包括:使用酰基-L-肉毒碱将待分析物质的样品进行酶水解, 肉碱酯酶。 酯酶由产碱杆菌属产生。 FERM BP-2570,它具有酰基-L-肉碱(包括短链酰基-L-肉碱)的底物特异性。 此外,酯酶显示乙酰基-L-肉碱和丙酰基-L-肉碱的底物特异性。 该酶促进1摩尔酰基-L-肉碱与1摩尔水的水解反应,其中形成1摩尔相应的脂肪酸和L-肉毒碱。 通过该方法测定形成的脂肪酸和L-肉毒碱的量。
Abstract:
A novel heteropolysaccharide S-184 is disclosed. The compound is a gum produced under suitable conditions by the novel microorganism Alcaligenes sp. This new heteropolysaccharide is composed primarily of carbohydrate as uronic acid (7% to 16%) and mannose, glucose, and galactose in the molar ratio of 1:3:5. The non-carbohydrate portion contains 12-16% protein and 3-4.5% acyl groups. The compound is used to alter viscosity and rheology of aqueous solutions.
Abstract:
The present invention generally relates to bacteriologically pure bacterial cultures of novel strains of plant growth-promoting bacteria, and inoculums comprising the same. The invention is also directed to plant seeds coated with the inoculums, kits comprising the inoculums and methods for stimulating plant growth by applying the biologically pure bacterial culture or the inoculum to a plant, plant seed, or plant growth medium.