Methods and compositions involving promoters derived from Yarrowia lipolytica
The current methods and compositions provide for nucleotide sequences of promoters from Yarrowia lipolytica which may be used to drive gene expression in a cell. In some aspects, the promoters are useful for modulating lipid production in oleaginous organisms such as yeast.
1. A nucleic acid molecule comprising:
a first sequence having at least 80% sequence identity to SEQ ID NO:1, 2, 5, 6 or 7, wherein the first sequence has promoter activity in a yeast cell; and
a second sequence operably linked to the first sequence, wherein the second sequence is heterologous to the first sequence, and wherein the second sequence comprises a coding sequence.
2. A yeast cell comprising the nucleic acid molecule of claim 1 .
3. The yeast cell of claim 2 , wherein the yeast cell is an Arxula adeninivorans, Candida utilis, Hansenula polymorpha, Kluyveromyces lactis, Kluyveromyces marxianus, Kodamaea ohmeri, Lipomyces lipofer, Lipomyces starkeyi, Lipomyces tetrasporus, Ogataea polymorpha, Pichia ciferrii, Pichia guilliermondii, Pichia pastoris, Pichia stipites, Rhodosporidium babjevae, Rhodosporidium toruloides, Rhodosporidium paludigenum, Rhodotorula glutinis, Rhodotorula mucilaginosa, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Wickerhamomyces ciferrii or Yarrowia lipolytica cell.
4. The yeast cell of claim 3 , wherein the yeast cell is a Yarrowia lipolytica.
5. A method comprising culturing the yeast cell of claim 2 under conditions sufficient to express the coding sequence.
6. The method of claim 5 , wherein the cell is cultured for at least 10 passages.
7. The method of claim 5 , wherein the coding sequence comprises SCT1.
8. The method of claim 5 , wherein yeast cell is a Yarrowia lipolytica.
9. The nucleic acid molecule of claim 1 , wherein the first sequence comprises SEQ ID NO:1, 2, 5, 6 or 7.
10. The nucleic acid molecule of claim 1 , wherein the second sequence is not from Yarrowia lipolytica.
11. The nucleic acid molecule of claim 1 , wherein the second sequence comprises SCT1.
12. The nucleic acid molecule of claim 1 , wherein the first sequence is a subsequence of SEQ ID NO:1, 2, 5, 6 or 7.
13. The nucleic acid molecule of claim 1 , wherein the first sequence is capable of inducing increased expression of the second sequence in a growth phase of a yeast cell relative to a lipid accumulation phase of the yeast cell.
14. The nucleic acid molecule of claim 1 , wherein the first sequence has at least 85% sequence identity to SEQ ID NO:1, 2, 5, 6 or 7.
15. The nucleic acid molecule of claim 1 , wherein the first sequence has at least 90% sequence identity to SEQ ID NO:1, 2, 5, 6 or 7.
16. The nucleic acid molecule of claim 1 , wherein the first sequence has at least 95% sequence identity to SEQ ID NO:1, 2, 5, 6 or 7.
17. The nucleic acid molecule of claim 1 , wherein the yeast cell is a Yarrowia lipolytica.
18. A method of optimizing lipid production of a cell during a fermentation process, wherein the fermentation process comprises a growth phase and a lipid accumulation phase, the method comprising:
(a) introducing into a cell a nucleic acid molecule comprising a promoter sequence having at least 80% sequence identity to SEQ IQ NO: 1, 2, 5, 6, or 7 to obtain a recombinant cell comprising the promoter sequence operably linked to a coding sequence, wherein the coding sequence is heterologous to the promoter sequence; and
(b) culturing the recombinant cell.
19. The method of claim 18 , wherein the coding sequence comprises SCT1.
20. A method of regulating the expression or activity of a coding sequence during a fermentation process wherein the fermentation process comprises a growth phase and a lipid accumulation phase, the method comprising:
(a) introducing a nucleic acid molecule into a yeast cell, wherein the nucleic acid molecule comprises the coding sequence operably linked to a promoter sequence, wherein the coding sequence is heterologous to the promoter sequence, and wherein the promoter sequence has at least 80% sequence identity to SEQ ID NO: 1, 2, 5, 6, or 7; and
(b) culturing the cell, thereby regulating expression or activity of the coding sequence.
21. The method of claim 20 , wherein the expression or activity of the coding sequence during the lipid accumulation phase is reduced by at least 90% as compared to the growth phase.
22. The method of claim 20 , wherein the cell is selected from the group consisting of Arxula adeninivorans, Candida utilis, Hansenula polymorpha, Kluyveromyces lactis, Kluyveromyces marxianus, Kodamaea ohmeri, Lipomyces hpofer, Lipomyces starkeyi, Lipomyces tetrasporus, Ogataea polymorpha, Pichia ciferrii, Pichia guilliermondii, Pichia pastoris, Pichia stipites, Rhodosporidium babjevae, Rhodosporidium toruloides, Rhodosporidium paludigenum, Rhodotorula glutinis, Rhodotorula mucilaginosa, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Wickerhamomyces ciferrii , and Yarrowia lipolytica.