Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

65 results about "Hansenula mrakii" patented technology

Novel Hansenula Polymorpha Gene Coding for Dolichyl-Phosphate- Mannose Dependent Alpha-1,3 Mannosyltransferase and Process for the Production of Recombinant Glycoproteins With Hansenula Polymorpha Mutant Strain Deficient in

The present invention relates to a process for producing a human-type glycoprotein having reduced glycosylation by genetically manipulating an enzyme involved in glycosylation using a Hansenula polymorpha system. In detail, the present invention relates to a process for producing a human-type glycoprotein by identifying a dolichyl-phosphate-mannose dependent ¥á-1,3-mannosyltransferase gene from H. polymorpha, constructing a H. polymorpha mutant strain producing a glycoprotein exhibiting reduced glycosylation by disrupting the identified gene, and subjecting the mutant strain to various genetic manipulations for the synthesis of human-type glycan.
Owner:KOREA RES INST OF BIOSCI & BIOTECH

Construction of recombinant eukaryotic hansenula engineering bacterial strains containing medical hirudin genes and production process of recombinant hirudin

The invention discloses construction of recombinant eukaryotic hansenula engineering bacterial strains containing medical hirudin genes and a production process of recombinant hirudin, wherein hansenula polytype host cell strains RB-11 are adopted as initial bacterial strains for constructing hansenula high-expression engineering bacterial strains RBHV 145-6 containing hirudin, and the hirudin with high purity and high content is obtained through culture and fermentation. In the invention, the hirudin genes are copied onto host cell chromosomes in a multi-copy mode, in addition, the copying number is kept stable, exogenous gene expression boxes containing the hirudin genes are completely integrated onto the host cell chromosomes, the existence of free plasmids in seed bank cells and passage 40 and 80 generation cells is avoided, the expression quantity and the secretion efficiency of foreign protein are 10 times higher than those of saccharomyces cerevisiae, particularly through beingcompared with that of the polytypic hansenula in China, the expression quantity of the foreign protein is high and is 35.8 percent, and in addition, the excessive glycosylation phenomenon does not exist, so the production process is suitable for target protein through large-scale fermentation production.
Owner:元昊 +1

Method for producing HPV45 L1 protein by using Hansenula polymorpha expression system

The invention relates to a method for producing HPV45 L1 protein by using a Hansenula polymorpha expression system. Specifically, the invention discloses a method for producing a recombinant Hansenula polymorpha cell expressing the HPV45 L1 protein and the recombinant Hansenula polymorpha cell produced by using the method. The invention further discloses a method for producing the HPV45 L1 protein by using the recombinant Hansenula polymorpha cell and application of the produced HPV45 L1 protein in preparation of prophylactic vaccines.
Owner:BEIJING ABZYMO BIOSCIENCES CO LTD +1

Composite microbial deodorizer and preparation method thereof

The invention discloses a composite microbial deodorizer and a preparation method thereof. According to the invention, thiobacillus ferrooxidans, rhizobium sludge, bacillus amyloliquefaciens, rhodopseudomonas palustris, pseudomonas stutzeri, bacillus coagulans and hansenula polymorpha are selected for use; liquid fermentation is performed respectively, and then compounding is performed in proportion; then linalool is added in proportion and the substances are fully mixed to prepare a composite microbial deodorizer capable of effectively expelling flies and insects, inhibiting growth and propagation of harmful flora and reducing and removing foul gas in the environment. The thiobacillus ferrooxidans (CFU/g) in the product is greater than or equal to 2.95*10<8>; the rhizobium sludge (CFU/g)is greater than or equal to 1.05*10<8>; the bacillus amyloliquefaciens (CFU/g) is greater than or equal to 1.73*10<8>; the rhodopseudomonas palustris (CFU/g) is larger than or equal to 2.55*10<8>; thepseudomonas stutzeri (CFU/g) is larger than or equal to 1.15*10<8>; the bacillus coagulans (CFU/g) is larger than or equal to 2.86*10<8>; the hansenula anomala (CFU/g) is larger than or equal to 2.97*10<8>; and the total amount of organic acids is larger than or equal to 25.8 g/L. The product provided by the invention has an obvious deodorization effect, the NH3 removal rate is greater than or equal to 78.14%, the H2S removal rate is greater than or equal to 71.64%, the odor concentration elimination rate is greater than or equal to 84.95%, and the mosquito and fly expelling rate is greater than or equal to 74.16%.
Owner:巴彦淖尔市云天下电子商务股份有限公司

Hansenula polymorpha for preparing high-lysine single-cell protein through methyl alcohol and application of Hansenula polymorpha

The invention relates to Hansenula polymorpha for preparing high-lysine single-cell protein through methyl alcohol and application of the Hansenula polymorpha. The classification name of the Hansenula polymorpha is Hansenula polymorpha AP23, the Hansenula polymorpha is preserved in the China Center for Type Culture Collection (CCTCC) on April 5th, 2016, and the preservation number is CCTCC No: M 2016173. By means of the plasma induced mutation technology, the strain capable of producing high-lysine single-cell protein is screened out with methyl alcohol as the only carbon source, and on this basis, the Hansenula polymorpha for efficiently utilizing methyl alcohol is screened out in a gradient mode through the further combination of methyl alcohol. By means of the strain, high-density fermentation can be achieved, methyl alcohol protein production is conducted through a 5 L fermentation tank, the final bacterium wet weight reaches 350-400 g / L, the methyl alcohol protein dry weight reaches 115-130 g / L, the protein content reaches 68%, and the lysine content reaches up to 60 mg / g. The Hansenula polymorpha has great social significance and economic value in development of animal feed protein additives.
Owner:NANJING UNIV OF TECH

Standard plasmid for detecting copy number of exogenous gene of recombinant CVA10 vaccine as well as preparation method and application of standard plasmid

The invention provides a standard plasmid for detecting the copy number of an exogenous gene of a recombinant CVA10 vaccine as well as a preparation method and application of the standard plasmid. The standard plasmid is formed by connecting an endogenous gene MOX fragment SEQ ID No.1, an exogenous gene P1 fragment SEQ ID No.2 and an exogenous gene 3CD fragment SEQ ID No.3 in series in a cloning vector. According to the method, the copy number of the inserted exogenous gene is simply, conveniently, rapidly, absolutely quantitatively and accurately analyzed by constructing the standard plasmid and adopting a Taqman probe-fluorescent quantitative PCR method, so that the detection time for determining the copy number of the exogenous gene of the recombinant CVA10 vaccine is effectively shortened, repeated operation is facilitated, and the detection efficiency is improved. The method has a wide application prospect in the determination of the copy number of the recombinant CVA10 vaccine exogenous gene constructed based on a hansenula polymorpha platform and the verification of the genetic stability of the recombinant CVA10 vaccine exogenous gene.
Owner:BEIJING MINHAI BIOTECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products