30results about How to "Increase the amount of fermentation" patented technology

The invention provides a method for producing L glutamic acid by fermentation. The method comprises the following steps: modifying a gene for coding DNA methylase on a chromosome of a corynebacteriumbacterium to reduce the activity and / or expression quantity of the DNA methylase; and producing the L glutamic acid by fermenting the bacterium obtained by modification. In addition, the invention also provides a method for treating glutamic acid fermentation liquor.

The invention provides a method for fermenting to produce L-lysine. The method includes replacing the promoter of one or more genes of the chromosome of the coryneform bacterium with the EP5 promoter, and modifying L-lysine produced by the bacterial fermentation. In addition, the invention also provides methods and applications derived from the method, as well as bacteria and promoters that can be used in these methods and applications.

The invention provides a fermenting production method of L-lysine. The method comprises a step of modifying bacteria to reduce not disappear the aconitase expression level or the enzymatic activity of the bacteria, and a step of fermenting the modified bacteria to produce L-lysine. The invention also provides processes derived from the method, applications thereof, and polynucleotides, vectors and bacteria used in the processes and the method and the applications.

The invention relates to the field of food waste deodorization equipment, in particular to a deodorization device for composting and fermentation of food waste, including a main body mechanism, a composting mechanism, a feeding mechanism, a material spreading mechanism and a shaking mechanism; The board runs through the side of the box body, slide the slider on the side wall of the board to the inside of the fixing seat on the side wall of the chain, the stepper motor is powered on to realize that the board for the food waste is lowered to a vacant position, and the next fixing seat is connected with the chain. Corresponding to the feed port, it is easy to install the next placing board. According to this method, several placing boards are installed to store the food waste for fermentation. After the garbage on the surface of the placing board at the bottom of the box is fermented into fertilizer, the bottom cover of the box can be opened The board realizes the cleaning of the fertilizer at the bottom of the box, so as to solve the problem of stratification of the traditional meal waste during the fermentation of the food waste, it can avoid that the fermented waste cannot be processed.

The invention provides a promoter nucleic acid sequence of sdaA gene, a recombinant strain containing the nucleic acid sequence and an application of the recombinant strain. The promoter is obtained by introducing a point mutation into a wild-type promoter sequence of sdaA gene. The recombinant strain is used for fermenting and producing L-lysine to further improve the yield of L-lysine, has no conflict with modification sites of other existing modified strains producing L-lysine, and realizes a new mode for improving the fermentation yield of L-lysine, and thus popularization and applicationare facilitated.

The invention provides a method for producing L-lysine through fermentation. The method comprises the following steps: modifying the bacteria to weaken but not vanish the expression of aconitase A and / or enzymatic activity, and producing L-lysine by using the modified bacteria through fermentation. In addition, the invention further provides a method and an application derived from the method, and polynucleotide, carriers and bacteria which can be applied to the methods and the application.

The invention provides a method for producing L-threonine through fermentation. The method comprises the steps of transforming the wild type regulatory element of an acnA gene on bacterial chromosome, so that the expression quantity of the aconitase A is lowered, but not disappear; and producing L-threonine through fermentation of the transformed bacteria. In addition, the invention also provides methods and applications derived from the method for producing L-threonine through fermentation, and bacteria used in the methods and applications.

The invention provides a method for fermentatively producing L-tryptophan, which comprises transforming the bacterial chromosome wxya The wild-type regulatory element of the gene, so that the regulatory element of the transformed bacterium has its downstream enzyme gene (such as, wxya The ability to initiate expression of the gene) is weakened but not disappeared; and, L-tryptophan is produced by fermentation with the transformed bacteria. In addition, the present invention also provides methods and uses derived from this method, as well as polynucleotides, vectors and bacteria that can be used in these methods and applications.

The invention provides a method for fermentatively producing l-threonine, which comprises transforming the wild-type regulatory element of the acnA gene on the bacterial chromosome so that the expression level of aconitase A is reduced but not eliminated; and, using the transformed bacterium Fermentation produces l-threonine. In addition, the present invention also provides methods and applications derived from this method, as well as bacteria and the like that can be used in these methods and applications.

The present invention provides a method for producing L-lysine by fermentation, which comprises modifying a wild-type ppc gene on the corynebacterium glutamicum chromosome; and fermenting the L-lysinewith the modified corynebacterium glutamicum. In addition, the present invention also provides a method and use derived by the method of the invention, as well as corynebacterium glutamicum, polynucleotides and the like which can be used in such methods and use.

The invention belongs to the technical field of microbial fermentation product extraction, and particularly relates to a method for efficiently extracting glucosamine from fermentation broth. On the basis of a method of extracting glucosamine with cation exchange resin in the prior art, a buffer solution of equilibrium activated resin is improved to effectively improve the adsorption efficiency ofthe resin to glucosamine, the saturated adsorption time of the resin is effectively shortened, the time of adsorption treatment is shortened, and the adsorption efficiency is effectively improved. Atthe same time, by improving an eluent in the existing method, glycine can effectively promote the connection of an amino group and the resin and helps to elute the target product, glucosamine, so asto effectively improve the efficiency of desorption process and improve the extraction rate of glucosamine in the fermentation broth on the whole.

The invention provides a method for producing L-lysine through fermentation. The method comprises the steps of transforming a promoter region of a wild-type ppc gene on a corynebacterium glutamicum chromosome and using corynebacterium glutamicum obtained through transformation to produce the L-lysine through fermentation. In addition, the invention further provides methods and application derivedfrom the method, as well as corynebacterium glutamicum, polynucleotides and the like which can be applied to the methods and application.

The invention provides a method for fermentatively producing L-tryptophan, which comprises transforming the bacterial chromosome fbp The wild-type regulatory element of the gene, so that the regulatory element of the transformed bacterium has its downstream enzyme gene (such as, fbp The ability to initiate expression of the gene) is weakened but not disappeared; and, L-tryptophan is produced by fermentation with the transformed bacteria. In addition, the present invention also provides methods and uses derived from this method, as well as polynucleotides, vectors and bacteria that can be used in these methods and applications.

The invention provides a method for fermentation production of L-tryptophan. The method comprises: transforming bacteria to reduce their tdcD enzyme expression quantity and / or enzyme activity, even to enable their tdcD enzyme expression quantity and / or enzyme activity to completely disappear; and, applying the transformed bacteria to fermentation production of L-tryptophan. In addition, the invention also provides methods derived from the method and application, as well as polynucleotide, carriers and bacteria usable in the methods and application.

The invention discloses a preparation method of Paecilomyces lilacinus fungus agent, which comprises the following steps: (1) mixing diatomaceous earth, corn flour and water at a mass ratio of 3:3:4 to obtain a solid medium; (2) fermenting: super Add every 200ml of PDB seed bacteria solution to 0.5kg solid medium in the clean bench. The spore concentration in the bacteria solution is 1010-1011cfu / ml. After stirring evenly, put it into a container with a thickness of 2.4-2.6cm, seal the container and ventilate it with oxygen. Sterilize, cultivate at a temperature of 25-28°C and a humidity of 25%-35%, and ferment for 7d-10d to obtain a solid fermented product; (3) make it into granules. At the same time, a fermentation device for Paecilomyces lilacinus agent is also disclosed, in which small holes are set on the side wall of the shallow dish, the small holes are blocked by sterile cotton balls or silica gel plugs, and the plastic film is hooped on the mouth of the shallow dish with rubber bands Edges sealed. The preparation method of the invention has simple process and low cost, is suitable for popularization and application, has simple device and is convenient to use.

The invention provides a method for producing L-threonine through fermentation. The method comprises the steps of transforming bacteria so that the expression quantity of aconitase A thereof and / or the enzyme activity are reduced but do not disappear, and fermenting the transformed bacteria to produce the L-threonine. In addition, the invention further provides a method and application derived from the method as well as a polynucleotide, a vector and bacteria applied in the methods and application.