46 results about "Comamonas" patented technology

Disclosed is an immunopotentiating composition comprising an effective immunostimulating substance which can activate natural immunity and a subsequent immunity mediated by lymphocytes without causing any damage to cells. Specifically disclosed is an immunopotentiating composition which is characterized by comprising, as an active ingredient, an immunostimulating substance produced by decomposing at least one bacterium selected from an MRE symbiotic bacteria group consisting of Bacillus sp. (FERM BP-11209), Lysinibacillus fusiformis (FERM BP-11206), Bacillus sonorensis, Lysinibacillus sp. (FERM BP-11207) and Comamonas sp. (FERM BP-11208).

Recalcitrant chemical oxygen demand (COD) of a liquid is reduced in a water treatment system. The method includes pretreating the liquid in a pretreatment unit to remove indigenous bacteria or microbes to a population level below which the indigenous organisms can interfere with the screened and externally introduced microorganisms. The liquid is then provided to a reactor that has a filter bed formed with a carrier material. Special microbes are screened and used to colonize the carrier material to remove recalcitrant COD. A biofilm is cultured on the surface of the carrier material to immobilize the screened microbes in the reactor. The method further includes percolating the liquid from the pretreatment unit through the filter bed colonized with the screened microbes to degrade at least part of the recalcitrant COD under aerobic conditions. In one embodiment, the filter is formed with biological granular activated carbon (GAC) as the carrier material and the screened microbes comprise at least one microbial species selected from the group consisting of Bacillus, Comamonas, Arthrobacter, Micrococcus, Pseudomonas, Pediococcus, Achromobacter, Flavobacterium, Mycobacterium, Rhodanobacter, Stenotrophomonas and Yeast.

The invention discloses a method for degrading polyethylene terephathalate. The method mainly includes the following steps: 1, strain culture: comamonas testoseroni strain is cultured for 12-18h in a solid medium with inclined surface at 30-37 DEG C; 2, substrate solution preparation: 5-9 parts of substrate solution with the concentration of 1-5g / L are prepared, each part is 50ml and is respectively placed into a 150ml conical flask, and packing up and sterilizing for 25min are carried out at 121 DEG C; 3, substrate degradation: the strain in the step 1 is inoculated into the substrate solution in the step 2, so as to obtain degradation liquor, and shake culture is carried out at the rotating speed of 200r / min and at the temperature of 30-37 DEG C, so as to catalyze degradation on the substrate; 4, substrate degradation ratio detection: 400-190nm wavelength scanning is adopted, and variation of substrate content is judged according to absorption peak at 240nm; 5, substrate degradationproduct detection: 400-190nm wavelength scanning is adopted, and variation of degradation intermediate product content is judged.