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AssigneeJiangnan University
InventorsJinsong Shi, Zhenghong Xu, Jinsong Gong, Haijuan Hou, Xiaomei Zhang, Heng Li
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The present invention provides a phospholipase D having an amino acid sequence as shown in SEQ ID NO. 1, and further provides a gene sequence encoding phospholipase D, which has a nucleotide sequence as shown in SEQ ID NO. 2. The present invention also provides a method for improving the expression level of phospholipase D by systematically engineering the expression elements. The method comprises screening and replacement of signal peptides, ribosome binding sites and promoters. The constructed recombinant plasmid is transformed into a host cell, and the recombinant strain is capable of successfully expressing phospholipase D. The phospholipase D of the present invention has a good phosphatidyl transferring ability, and can be used for synthesizing the product phosphatidylserine with lecithin and L-serine as substrates. The recombinant strain has good stability of enzyme activity and short fermentation period, which lays the foundation for large-scale industrial production.
A transgenic cell line comprising a polynucleotide that comprises the nucleotide sequence of SEQ ID NO:
A recombinant plasmid that comprises a gene encoding a phospholipase D, wherein said gene comprises SEQ ID NO:2, a nucleic acid encoding a signal peptide, wherein said nucleic acid comprises SEQ ID NO:3, a ribosome binding site that comprises SEQ ID NO:4, and a promoter that comprises SEQ ID NO:5.
A recombinant strain expressing a phospholipase D, wherein said recombinant strain is obtained by introducing a recombinant plasmid that comprises a gene encoding a phospholipase D, wherein said gene comprises SEQ ID NO:2, a nucleic acid encoding a signal peptide, wherein said nucleic acid comprises SEQ ID NO:3, a ribosome binding site that comprises SEQ ID NO:4, and a promoter that comprises SEQ ID NO:5.
Dependencies are inferred from the claim text.