Abstract
Campesterol is an important precursor for many sterol drugs, e.g. progesterone and hydrocortisone. In order to produce campesterol in Yarrowia lipolytica, C-22 desaturase encoding gene ERG5 was disrupted and the heterologous 7-dehydrocholesterol reductase (DHCR7) encoding gene was constitutively expressed. The codon-optimized DHCR7 from Rallus norvegicus, Oryza saliva and Xenapus laevis were explored and the strain with the gene DHCR7 from X. laevis achieved the highest titer of campesterol due to D409 in substrate binding sites. In presence of glucose as the carbon source, higher biomass conversion yield and product yield were achieved in shake flask compared to that using glycerol and sunflower seed oil. Nevertheless, better cell growth rate was observed in medium with sunflower seed oil as the sole carbon source. Through high cell density fed-batch fermentation under carbon source restriction strategy, a titer of 453±24.7 mg/L campesterol was achieved with sunflower seed oil as the carbon source, which is the highest reported microbial titer known. Our study has greatly enhanced campesterol accumulation in Y. lipolytica, providing new insight into producing complex and desired molecules in microbes.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Amino Acid Sequence
-
Animals
-
Bacterial Proteins / genetics*
-
Binding Sites
-
Biomass
-
Bioreactors
-
Carbon / chemistry
-
Cholesterol / analogs & derivatives*
-
Cholesterol / biosynthesis
-
Cytochrome P-450 Enzyme System / genetics
-
Fermentation
-
Genetic Engineering / methods*
-
Glucose / chemistry
-
Glycerol / chemistry
-
Industrial Microbiology
-
Lipids / chemistry
-
Molecular Sequence Data
-
Oryza / metabolism
-
Oxidoreductases Acting on CH-CH Group Donors / genetics*
-
Phytosterols / biosynthesis*
-
Plant Oils
-
Rats
-
Sequence Homology, Amino Acid
-
Sunflower Oil
-
Xenopus laevis
-
Yarrowia / genetics*
Substances
-
Bacterial Proteins
-
Lipids
-
Phytosterols
-
Plant Oils
-
Sunflower Oil
-
campesterol
-
Carbon
-
Cytochrome P-450 Enzyme System
-
Cholesterol
-
Oxidoreductases Acting on CH-CH Group Donors
-
7-dehydrocholesterol reductase
-
Glucose
-
Glycerol
Grants and funding
This work was supported by the Ministry of Science and Technology of China ("863" Program: 2012AA02A701), the National Natural Science Foundation of China (21390203 and 21206114) and Natural Science Foundation of Tianjin (12JCQNJC03800). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.