Patent classifications
C12N11/10
BACILLUS SP. SDC-U1 STRAIN WITH QUORUM QUENCHING ACTIVITY, COMPOSITION FOR INHIBITING BIOFILM INCLUDING THE SAME AND SYSTEM FOR TREATING WATER USING THE SAME FOR MEMBRANE BIOREACTOR
Bacillus sp. SDC-U1 strain deposited to Korean Collection for Type Cultures with Accession No. KCTC 14857BP has quorum quenching activity.
BACILLUS SP. SDC-U1 STRAIN WITH QUORUM QUENCHING ACTIVITY, COMPOSITION FOR INHIBITING BIOFILM INCLUDING THE SAME AND SYSTEM FOR TREATING WATER USING THE SAME FOR MEMBRANE BIOREACTOR
Bacillus sp. SDC-U1 strain deposited to Korean Collection for Type Cultures with Accession No. KCTC 14857BP has quorum quenching activity.
Programmable and Printable Biofilms as Engineered Living Materials
Three-dimensional, living, self-regenerative structures of predetermined geometry comprising solidified print material comprising a biofilm of Bacillus subtilis comprise a TasA-R protein, wherein R is a recombinant, heterologous functional group, wherein the TasA-R provides a preferably tunable physiochemical property like viscosity, reactivity, affinity as a function of the R group.
Programmable and Printable Biofilms as Engineered Living Materials
Three-dimensional, living, self-regenerative structures of predetermined geometry comprising solidified print material comprising a biofilm of Bacillus subtilis comprise a TasA-R protein, wherein R is a recombinant, heterologous functional group, wherein the TasA-R provides a preferably tunable physiochemical property like viscosity, reactivity, affinity as a function of the R group.
IMPROVED FORMULATIONS FOR PANCREATIC ISLET ENCAPSULATION
Provided herein according to embodiments of the present invention is a microcapsule comprising: (a) one or more live mammalian pancreatic islet cells; and (b) an alginate composition encapsulating said islet cells, wherein said alginate composition comprises extracellular matrix proteins solubilized or suspended therein. Compositions comprising a plurality of the microcapsules and the use thereof in treating type I diabetes are also provided.
IMPROVED FORMULATIONS FOR PANCREATIC ISLET ENCAPSULATION
Provided herein according to embodiments of the present invention is a microcapsule comprising: (a) one or more live mammalian pancreatic islet cells; and (b) an alginate composition encapsulating said islet cells, wherein said alginate composition comprises extracellular matrix proteins solubilized or suspended therein. Compositions comprising a plurality of the microcapsules and the use thereof in treating type I diabetes are also provided.
Engineered proline hydroxylase polypeptides and methods
The present disclosure provides engineered proline hydroxylase polypeptides for the production of hydroxylated compounds, polynucleotides encoding the engineered proline hydroxylases, host cells capable of expressing the engineered proline hydroxylases, and methods of using the engineered proline hydroxylases to prepare compounds useful in the production of active pharmaceutical agents.
ENZYME FORMULATION AND METHOD FOR DEGRADATION
An enzyme formulation includes an encapsulated fungal enzyme which is effective for degrading at least one material selected from the group consisting of hydrocarbons, vulcanized rubber, synthetic rubber, natural rubber, vulcanized polymers and perfluorinated compounds. A degradation method includes treating one of the above-mentioned materials with an encapsulated fungal enzyme to degrade the material.
ENZYME FORMULATION AND METHOD FOR DEGRADATION
An enzyme formulation includes an encapsulated fungal enzyme which is effective for degrading at least one material selected from the group consisting of hydrocarbons, vulcanized rubber, synthetic rubber, natural rubber, vulcanized polymers and perfluorinated compounds. A degradation method includes treating one of the above-mentioned materials with an encapsulated fungal enzyme to degrade the material.
MULTI-FUNCTIONAL OXYGENATING MICROPARTICLE LOADED CELL AGGREGATES
A method of preparing and obtaining cell aggregates having increased oxygenation abilities. The method includes the preparation of fluorinated polymeric microparticles. Once the fluorinated polymeric microparticles are prepared, they are combined with mammalian cells to create the cell aggregates having increased oxygenation.