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US 11,111,485 B2Granted
Expression system for Psicose epimerase and production for Psicose using the same
AssigneeSamyang Corporation
InventorsJin Sol Heo, Hye Jung Kim, Min Jeong Kim, Jeong Yoon Choi, Chong Jin Park, Kang Pyo Lee
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Abstract
A gene expression cassette capable of producing psicose at high yield with high stability, a GRAS (Generally recognized as safe) microorganism, a method of producing the enzyme by using the GRAS microorganism, and a method of producing the psicose by using the GRAS microorganism and enzyme are provided.
Claims16
A method of producing a psicose epimerase, comprising:
- culturing a recombinant Corynebacterium sp. cell transformed by a vector comprising a gene expression cassette, and
- reacting a fructose-containing substrate with at least one selected from the group consisting of an psicose epimerase obtained from the culture of the recombinant Corynebacterium sp., a recombinant cell, a culture of the recombinant cell, a lysate of the recombinant cell and an extract of cell culture or the cell lysate, and
- wherein the gene expression cassette, producing a psicose epimerase in Corynebacterium sp., and comprising:
- a nucleotide sequence encoding the psicose epimerase;
- and
- a regulating sequence being operably connected to the nucleotide sequence in the upstream regulating the expression of the nucleotide sequence in Corynebacterium sp., and comprising a promoter, a ribosome binding site (RBS) sequence and a first spacer sequence in the direction of 5′ to 3′,
- wherein the promoter includes the nucleotide sequence of SEQ ID NO:
- 1,
- the ribosome binding site (RBS) sequence is a nucleotide sequence in a size of 7 to 20 bases including the nucleotide sequence of SEQ ID NO:
- 2, and
- the first spacer sequence is selected from the group consisting of the nucleotide sequences of SEQ ID NO:
- 4 to SEQ ID NO:
- 6.
10 more elements
Dependencies are inferred from the claim text.