Method for obtaining a microbial strain for production of sphingoid bases
View Patent ↗The present invention provides genetically engineered microbial strains, in particular genetically engineered yeast strains, that produce at least 0.5 mg per g CDW of a sphingoid base according to Formula I or a salt or ester thereof. The present invention provides a method to obtain genetically engineered microbial strains producing at least 0.5 mg per g CDW of a sphingoid base according to Formula I or a salt or ester thereof. The method comprises the steps of: a) increasing the expression of a polynucleotide encoding an enzyme having ceramide synthase activity and/or an enzyme having ceramidase activity, the latter being capable of preferentially, or even specifically, hydrolyzing ceramides containing a sphingoid base according to Formula I, and/or b) decreasing the expression of a polynucleotide encoding an enzyme having sphingolipid Δ8-desaturase activity and/or an enzyme having ceramidase activity, the latter being capable of preferentially, or even specifically, hydrolyzing ceramides containing phytosphingosine or dihydrosphingosine as sphingoid base, and isolating strains with the required productivity.
1. A method to obtain a Pichia ciferrii strain that produces at least 0.5 mg per g cell dry weight of sphingosine and triacetylated sphingosine comprising
obtaining a syringomycinE-resistant Pichia ciferrii strain defective in dihydrosphingosine C-4 hydroxylase;
inactivating or deleting a genomic sphingolipid Δ8-desaturase (8DES) gene encoding a polypeptide comprising the amino acid sequence of SEQ ID NO:6 and/or inactivating a genomic alkaline ceramidase (YXC1) gene encoding a polypeptide comprising the amino acid sequence of SEQ ID NO:8 in the syringomycinE-resistant Pichia ciferrii strain defective in dihydrosphingosine C-4 hydroxylase;
increasing expression of
i) a polynucleotide encoding an enzyme having dihydroceramide-Δ4-desaturase activity and comprising the amino acid sequence of SEQ ID NO:17 or an amino acid sequence that has at least 90% identity to the amino acid sequence of SEQ ID NO:17,
ii) a polynucleotide encoding an enzyme having ceramidase activity, said ceramidase hydrolyzing sphingosine and triacetylated sphingosine, and comprising the amino acid sequence of SEQ ID NO:15 or an amino acid sequence that has at least 90% identity to the amino acid sequence of SEQ ID NO:15, and
iii) a polynucleotide encoding an enzyme having ceramide synthase activity and comprising the amino acid sequence of SEQ ID NO:2, 4, 9, 10, 12, or 14 or an amino acid sequence that has at least 90% identity to the amino acid sequence of SEQ ID NO:2, 4, 9, or 10,
wherein increasing expression is by transformation of the Pichia ciferrii strain with the polynucleotides and optionally integrating one or several copies of the polynucleotides into the chromosome of the Pichia ciferrii strain; and
isolating a Pichia ciferrii strain that produces at least 0.5 mg per g cell dry weight of sphingosine and triacetylated sphingosine.
2. The method according to claim 1 wherein inactivation or deletion of the genomic 8DES gene and inactivation or deletion of the genomic YXC1 gene comprises deletion of portions of the nucleotide sequence or deletion of the entire nucleotide sequence.
3. The method according to claim 1 , wherein the enzyme having ceramide synthase activity is selected from the group consisting of:
a. a polypeptide with the amino acid sequence of SEQ ID NO:2 or SEQ ID NO:4,
b. a polypeptide with an amino acid sequence having at least 90% amino acid sequence identity to the amino acid sequence of SEQ ID NO:2 or at least 90% amino acid sequence identity to the amino acid sequence of SEQ ID NO:4,
c. a polypeptide with the amino acid sequence of SEQ ID NO:9,
d. a polypeptide with an amino acid sequence having at least 90% amino acid sequence identity to the amino acid of SEQ ID NO:9,
e. a polypeptide with the amino acid sequence of SEQ ID NO: 10, and
f. a polypeptide with an amino acid sequence having at least 90% amino acid sequence identity to the amino acid sequence of SEQ ID NO: 10.
4. The method according to claim 1 , wherein the genomic 8DES gene comprises the nucleotide sequence of SEQ ID NO: 5.
5. The method according to claim 1 , wherein the genomic alkaline ceramidase (YXC1) gene comprises the nucleotide sequence of SEQ ID NO:7.
6. The method according to claim 1 , wherein the enzyme having dihydroceramide-Δ4-desaturase activity comprises the amino acid sequence of SEQ ID NO: 17.
7. The method according to claim 1 , wherein increasing the expression is by transformation of the Pichia ciferrii strain with the polynucleotides.
8. A method to obtain an Ashbya gossypii strain that produces at least 0.5 mg per g cell dry weight of sphingosine and triacetylated sphingosine comprising
inactivating or deleting a genomic sphinganine hydroxylase (SYR2) gene encoding a polypeptide having sphinganine hydroxylase activity, wherein the polypeptide having sphinganine hydroxylase activity is encoded by the polynucleotide of SEQ ID NO:23 and inactivating or deleting a genomic sphingolipid Δ8 desaturase (8DES) gene encoding a polypeptide comprising the amino acid sequence of SEQ ID NO:21 in a Ashbya gossypii strain;
increasing expression of
i) a polynucleotide encoding an enzyme having dihydroceramide-Δ4-desaturase activity and comprising the amino acid sequence of SEQ ID NO:16,
ii) a polynucleotide encoding an enzyme having ceramide synthase activity and comprising the amino acid sequence of SEQ ID NO:12 or 14,
wherein increasing expression is by transformation of the Ashbya gossypii strain with the polynucleotides and optionally integrating one or several copies of the polynucleotides into the chromosome of the Ashbya gossypii strain; and
isolating said Ashbya gossypii strain that produces at least 0.5 mg per g cell dry weight of sphingosine and triacetylated sphingosine.
9. The method according to claim 8 , wherein inactivation or deletion of the genomic 8DES gene and inactivation or deletion of the genomic SYR2 gene comprises deletion of portions of the nucleotide sequence or deletion of the entire nucleotide sequence.
10. The method according to claim 8 , wherein increasing expression is by transformation of the Ashbya gossypii strain with the polynucleotides.