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1.
J Biosci Bioeng ; 131(6): 613-621, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33582014

ABSTRACT

The oleaginous yeast Lipomyces starkeyi is an intriguing lipid producer that can produce triacylglycerol (TAG), a feedstock for biodiesel production. We previously reported that the L. starkeyi mutant E15 with high levels of TAG production compared with the wild-type was efficiently obtained using Percoll density gradient centrifugation. However, considering its use for biodiesel production, it is necessary to further improve the lipid productivity of the mutant. In this study, we aimed to obtain mutants with better lipid productivity than E15, evaluate its lipid productivity, and analyze lipid synthesis-related gene expression in the wild-type and mutant strains. The mutants E15-11, E15-15, and E15-25 exhibiting higher lipid productivity than E15 were efficiently isolated from cells exposed to ultraviolet light using Percoll density gradient centrifugation. They exhibited approximately 4.5-fold higher lipid productivity than the wild-type on day 3. The obtained mutants did not exhibit significantly different fatty acid profiles than the wild-type and E15 mutant strains. E15-11, E15-15, and E15-25 exhibited higher expression of acyl-CoA synthesis- and Kennedy pathway-related genes than the wild-type and E15 mutant strains. Activation of the pentose phosphate pathway, which supplies NADPH, was also observed. These results suggested that the increased expression of acyl-CoA synthesis- and Kennedy pathway-related genes plays a vital role in lipid productivity in the oleaginous yeast L. starkeyi.


Subject(s)
Lipids/biosynthesis , Lipomyces , Ultraviolet Rays , Biofuels , Fatty Acids/metabolism , Gene Expression Regulation, Fungal/radiation effects , Lipid Metabolism/genetics , Lipid Metabolism/radiation effects , Lipids/radiation effects , Lipomyces/genetics , Lipomyces/isolation & purification , Lipomyces/metabolism , Lipomyces/radiation effects , Metabolic Engineering , Organisms, Genetically Modified , Pentose Phosphate Pathway/genetics , Pentose Phosphate Pathway/radiation effects , Triglycerides/metabolism , Yeasts/genetics , Yeasts/metabolism , Yeasts/radiation effects
2.
Appl Microbiol Biotechnol ; 103(15): 6297-6308, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31165226

ABSTRACT

The oleaginous yeast Lipomyces starkeyi is an attractive organism for the industrial production of lipids; however, the amount of lipid produced by wild-type L. starkeyi is insufficient. The study aims to obtain L. starkeyi mutants that rapidly accumulate large amounts of triacylglycerol (TAG). Mutagenized yeast cells at the early stages of cultivation were subjected to Percoll density gradient centrifugation; cells with increased production of TAG were expected to be enriched in the resultant upper fraction because of their lower density. Among 120 candidates from the upper fractions, five mutants were isolated that accumulated higher amounts of TAG. Moreover, when omitting cells with mucoid colony morphology, 11 objective mutants from 11 candidates from the upper fraction were effectively (100%) isolated. Of total 16 mutants obtained, detailed characterization of five mutants was performed to reveal that five mutants achieved about 1.5-2.0 times TAG concentration (4.7-6.0 g/L) as compared with the wild-type strain (3.6 g/L) at day 5. Among these five mutants, strain E15 was the best for industrial use because only strain E15 showed significantly higher TAG concentration as well as significantly higher degree of lipid to glucose and biomass to glucose yields than the wild-type strain. Thus, Percoll density gradient centrifugation is an effective method to isolate mutant cells that rapidly accumulate large amounts of TAG. It is expected that by repeating this procedure as part of a yeast-breeding program, L. starkeyi mutants suitable for industrial lipid production can be easily and effectively obtained.


Subject(s)
Lipomyces/genetics , Lipomyces/metabolism , Metabolic Networks and Pathways/genetics , Mutation , Triglycerides/metabolism , Industrial Microbiology/methods , Lipomyces/isolation & purification , Metabolic Engineering/methods , Mutagenesis
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