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59results about How to "High flocculation activity" patented technology

Extra-cellular polysaccharide of aerobic Ruthia sp. strain metabolin and preparation and application thereof

The invention relates to an extra-cellular polysaccharide of aerobic Ruthia sp. strain metabolin and preparation and application thereof. An aerobic strain ZHT4-13 is separated from adhesive sludge of wild Ruditapes philippinarums in the Bohai sea offshore of China and is identified as a Ruthia sp. The aerobic strain is treated by seed culture and amplification culture, and a fermentation broth of the aerobic strain is precipitated with ethanol and separated centrifugally to obtain the extra-cellular polysaccharide MBF4-13. The extra-cellular polysaccharide MBF4-13 is measured to have high flocculation activity, the FR value to kaolin reaches over 80 percent, and the removal rate to hexavalent chromium ions reaches 69.3 percent; the extra-cellular polysaccharide MBF4-13 has high activity to decolorize high-concentration wastewater, and the decolorization ratios to methylene blue, ink blue, malachite green and crystal violet reach 86.11 percent, 99.49 percent and 97.84 percent; and the extra-cellular polysaccharide MBF4-13 plays a role of obviously improving the performance and the structure of activated sludge. The extra-cellular polysaccharide has potential value of developing a novel microbial flocculant.
Owner:DALIAN JIAOTONG UNIVERSITY

Bacillus licheniformis gene engineering bacterium capable of producing polysaccharide flocculant at high yield and establishment method thereof

The invention relates to a Bacillus licheniformis gene engineering bacterium capable of producing a polysaccharide flocculant at high yield and an establishment method thereof, belonging to the technical fields of gene engineering and microbial fermentation. The gene engineering bacterium is formed by overexpressing epsDEF gene in Bacillus licheniformis. The nucleotide sequence of the epsDEF gene is disclosed as SEQ ID No 1 in the sequence table. The gene engineering bacterium preparation method comprises the following steps: cloning the epsDEF gene into an expression vector to obtain a recombinant expression vector, and transforming the recombinant expression vector into extracellular-polysaccharide-producing Bacillus licheniformis by electric transformation, thereby obtaining the gene engineering bacterium capable of producing a polysaccharide flocculant at high yield. The polysaccharide flocculant preparation method comprises the following steps: carrying out fermentation and culture on the gene engineering bacterium, collecting the fermentation liquid, and purifying to obtain the polysaccharide flocculant. In the gene engineering bacterium fermentation process, the flocculation activity of the fermentation liquid is obviously enhanced, and the polysaccharide flocculant yield is obviously enhanced. The polysaccharide flocculant is applicable to sewage treatment and food engineering.
Owner:XIAMEN UNIV

Bacillus licheniformis, method for preparing flocculating agent from bacillus licheniformis and application of flocculating agent

The invention relates to bacillus licheniformis, a method for preparing a flocculating agent from the bacillus licheniformis and an application of the flocculating agent. The strain is bacillus licheniformis LZ-1 which is preserved in China General Microbiological Culture Collection Center on November 06, 2012 with preservation number of CGMCC No.6782. With the application of the bacillus licheniformis LZ-1 as well as a production method provided by the invention, a fermentation broth, which is high in flocculating activity, is obtained under the condition that an initial pH value is alkaline, and high-molecular-weight polysaccharide, which is 0.8-3.2*10<7>Da, serves as a major flocculating active ingredient. The polysaccharide flocculating agent provided by the invention has the advantages of being high in flocculating activity, low in dosage, low in production cost and the like, and the flocculating agent has a flocculating conditioning effect on sludge. The bacillus licheniformis LZ-1 fermentation broth or a product, which is extracted from the fermentation broth and contains the polysaccharide flocculating agent, can be applied to deep dewatering by sludge plate-frame pressure filtration in a mode of replacing a polyacrylamide flocculating agent, so that sewage treatment plant concentrated sludge, which is 96-98% in moisture content, is further dewatered into a sludge cake which is lower than 60% in moisture content and the size of the sludge is diminished to be 1/20-1/10 of an original size.
Owner:INST OF MICROBIOLOGY - CHINESE ACAD OF SCI +2

Extra-cellular polysaccharide of aerobic Ruthia sp. strain metabolin and preparation and application thereof

The invention relates to an extra-cellular polysaccharide of aerobic Ruthia sp. strain metabolin and preparation and application thereof. An aerobic strain ZHT4-13 is separated from adhesive sludge ofwild Ruditapes philippinarums in the Bohai sea offshore of China and is identified as a Ruthia sp. The aerobic strain is treated by seed culture and amplification culture, and a fermentation broth ofthe aerobic strain is precipitated with ethanol and separated centrifugally to obtain the extra-cellular polysaccharide MBF4-13. The extra-cellular polysaccharide MBF4-13 is measured to have high flocculation activity, the FR value to kaolin reaches over 80 percent, and the removal rate to hexavalent chromium ions reaches 69.3 percent; the extra-cellular polysaccharide MBF4-13 has high activity to decolorize high-concentration wastewater, and the decolorization ratios to methylene blue, ink blue, malachite green and crystal violet reach 86.11 percent, 99.49 percent and 97.84 percent; and theextra-cellular polysaccharide MBF4-13 plays a role of obviously improving the performance and the structure of activated sludge. The extra-cellular polysaccharide has potential value of developing a novel microbial flocculant.
Owner:DALIAN JIAOTONG UNIVERSITY

Carrier-free immobilized culture method of microbial flocculating agent

The invention discloses a carrier-free immobilized culture method of a microbial flocculating agent. The method is characterized by comprising the following steps of: adding self-flocculating bacteria spore suspension in a volume which is 0.1 to 1 percent of the volume of a culture medium into the culture medium, wherein each millimeter of suspension contains 106 self-flocculating bacteria spores; putting the culture medium into a shaking bed, and performing culture and fermentation, wherein the culture conditions comprise that the revolution speed is 150 to 180 revolutions per minute, the temperature is 20 to 30 DEG C and the pH is 3.5 to 10.5; and standing after the suspension is cultured for 24 to 120 hours, and separating mycelium pellets generated by the self-flocculating bacteria and the fermentation solution, wherein the solid part is the mycelium pellets, and the liquid part is the microbial flocculating agent. Sucrose is used as a carbon source, sodium nitrate is used as a nitrogen source, the self-flocculating bacteria generate stress reaction by using the characteristic that the self-flocculating bacteria can form the mycelium pellets and improving the salt concentration of the culture medium, and the purpose of generating the microbial flocculating agent by the self-flocculating bacteria is fulfilled. The microbial flocculating agent prepared by the method has the advantages of low cost, extensive production conditions and high flocculating activity, and can be used for treating multiple kinds of printing and dyeing wastewater.
Owner:JINGGANGSHAN UNIVERSITY

Method for preparing microbial flocculant by protoplast fusion technology

The invention provides a method for preparing a microbial flocculant by a protoplast fusion technology, and belongs to the field of flocculant preparation. The method is characterized by (1) protoplast producing bacterium LV-1 regeneration conditions and preparation steps, specifically comprising carrying out an activation operation in a liquid complete medium (CM) for 5 to 10 hours based on an inoculation amount of 0.5 to 2%, adding 2 to 6 mol/L of glycine into the liquid complete medium before enzymolysis to carry out a treatment for 5 to 15 hours, carrying out an enzymolysis process in a water bath for 1 to 4 hours at a temperature of 37 DEG C and an enzyme concentration of 0.05 to 0.2 mg/mL, and coating a regeneration template containing cane sugar as a stabilizer, and (2) protoplast fusion strain LV-2 fermentation and flocculation conditions, specifically comprising a cane sugar content of 8 to 12 g/L, a lactose content of 5 to 10 g/L, an ammonium nitrate content of 0.4 to 1.2 g/L, a peptone content of 0.4 to 1.2 g/t, an extract yeast content of 0.1 to 0.4 g/L, a culture temperature of 20 to 40 DEG C and an optimal adding amount of 0.2 to 2%. Compared with the prior art, the method has the advantages of high effectiveness, simple process, board application scope, low cost and good biological safety.
Owner:SHANGHAI GREEN LIFE ENVIRONMENTAL PROTECTION TECH

Method for preparing microbial flocculant through enteromorpha hydrolysate fermentation

The invention discloses a method for preparing a microbial flocculant through enteromorpha hydrolysate fermentation. The method comprises the steps of preparation of liquid strain, fermentation and product aftertreatment. The fermentation process comprises the steps that 1, fresh enteromorpha is cleaned, salt, sediment and unwanted algae are removed, then the fresh enteromorpha is smashed and added to a hydrolysis tank, water is added to regulate acidity, alkali is added for neutralization, filter pressing and clarification are conducted, and then a hydrolysate is obtained; 2, the hydrolysate is diluted till the sugar concentration of reducing sugar is 15-30 g / L, fermentation liquor is prepared and added to a fermentation tank, and high-temperature sterilization and cooling are conducted; 3, a seed solution is inoculated into the fermentation tank for fermentation, and fermentation is ended after the content of residual sugar in the fermentation liquor is reduced to the level below 3 g / L. According to the method, enteromorpha is used as the raw material, microbial flocculant fermentation is directly conducted after acid hydrolysis filtration, the production method is simple, production cost is low, grain is saved, and waste is turned into wealth.
Owner:青岛美能达生物科技有限公司

Radiation resistant pantoea sp. W36-1 and application thereof in environmental engineering

The invention discloses pantoea sp. W36-1, of which the preservation number is CGMCC No. is 3701, a flocculant prepared by the pantoea sp. W36-1 and application of the flocculant in removal of suspensions, dyeing agents and heavy metal in waste water. Extracellular products of the bacteria have an obvious absorption peak at 200 to 250nm, and polysaccharide solution can remove 54.89 percent of free groups in the bacteria. The method for preparing the pantoea sp. W36-1 comprises the following steps of: performing fermentation culture of the bacteria strain for 48 hours, centrifuging 100ml of fermentation solution at a rotation speed of 6,000r / min for 10 minutes, adding absolute ethanol, of which the volume is 1.5 times that of supernatant, into the supernatant, uniformly mixing the absoluteethanol and the supernatant standing the mixed solution at the temperature of 4 DEG C overnight, centrifuging the precipitate, washing the precipitate by 70-percent ethanol for 2 to 3 times, and thendrying the precipitate to obtain the finished product. The flocculent activity of the fermentation culture product of the pantoea sp. W36-1 is 81.7 to 83.15 percent, the yield of the pantoea sp. W36-1 is 6g / L and can be widely used for removing suspensions, dyeing agents, heavy metal and the like in waste water.
Owner:THE INST OF MICROBIOLOGY XINJIANG ACADEMY OF AGRI SCI

A kind of anti-high temperature floc producing strain and its cultivation and application method

The invention relates to a high-temperature-resistant flocculant-producing bacterial strain, and cultivation and application methods thereof, and belongs to the field of microbiology. The high-temperature-resistant flocculant-producing bacterial strain is preserved by China General Microbiological Culture Collection Center (CGMCC), wherein the preservation number is CGMCC No.2040; the classification and nomenclature is Paenibacillus sp.; the preservation date is May 11, 2007. High-temperature-resistant paenibacillus screened from soil of fruit trees is a new bacterium which is discovered in China for the first time; the high-temperature-resistant paenibacillus is heated at a high temperature of 40 to 80 DEG C for 5 to 60 minutes and then is subjected to aerated fermentation culture at 25 to 35 DEG C; when the fermentation liquid is applied to kaolin suspension flocculant, the flocculation ratio is 88% to 97% when the proportion is 0.01% to 0.2% (v / v). When the paenibacillus provided by the invention and the fermentation liquid thereof are applied to the kaolin suspension flocculant, the culture operating process is simple and convenient, the cost is low, the flocculation activity is high, the using amount is small and secondary pollution is avoided.
Owner:NORTHEASTERN UNIV LIAONING
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