Abstract:
Provided are a recombinant protein, a gene encoding the recombinant protein, a recombinant microorganism including the gene, and a method of degrading a macromolecular substance using the recombinant microorganism or the recombinant protein.
Abstract:
Provided are a vector replicable in E. coli and a cell of the genus Komagataeibacter, a cell including the same, a method of producing a target protein using the cell, or a method of evaluating a candidate promoter using the cell.
Abstract:
A genetically modified microorganism of the genus Gluconacetobacter has decreased pyrroloquinoline-quinone (PQQ)-dependent glucose dehydrogenase (GDH) activity of and increased glucose permease activity. The microorganism has enhanced productivity cellulose and is useful for the manufacture of microbial cellulose.
Abstract:
A genetically engineered bacteria cell having an enhanced activity of GlnD or GlnK, and a method of producing succinic acid by using the genetically engineered bacteria cell are provided.
Abstract:
A microorganism capable of producing an acrylic acid (AA), wherein activities of a pathway producing AA through conversions of 3-HP to 3-HP-CoA and 3-HP-CoA to AA-CoA in the microorganisms are increased; as well as a method of producing the microorganism and a method of producing an acrylic acid by using the same.
Abstract:
A microorganism capable of producing an acrylic acid (AA), wherein activities of a pathway producing AA through conversions of 3-HP to 3-HP-CoA and 3-HP-CoA to AA-CoA in the microorganisms are increased; as well as a method of producing the microorganism and a method of producing an acrylic acid by using the same.
Abstract:
A genetically engineered bacterial cell wherein activity of a pathway in the cell of converting α-ketoglutarate into succinate semialdehyde; or activity of succinyl semialdehyde dehydrogenase in the cell is increased compared to the activity in a non-genetically engineered cell of the same type, and a method of producing succinic acid by using the same.