1. Analysis of the light regulatory mechanism in carotenoid production in Rhodosporidium toruloides NBRC 10032
- Author
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Atsushi Yamazaki, Yuuki Hakozaki, Satoru Kuhara, Takeru Takamizawa, Yosuke Shida, Kazuki Mori, Khanh Dung Pham, Wataru Ogasawara, Hiroaki Takaku, Harutake Yamazaki, Kosuke Tashiro, and Sachiyo Aburatani
- Subjects
Light ,Genes, Fungal ,Mutant ,Rhodosporidium toruloides ,Polymorphism, Single Nucleotide ,Applied Microbiology and Biotechnology ,Biochemistry ,Analytical Chemistry ,03 medical and health sciences ,Cryptochrome ,Gene expression ,Molecular Biology ,Gene ,030304 developmental biology ,Regulation of gene expression ,0303 health sciences ,biology ,030306 microbiology ,Chemistry ,fungi ,Organic Chemistry ,Rhodotorula ,General Medicine ,biology.organism_classification ,Carotenoids ,Yeast ,Cell biology ,Cryptochromes ,Non-homologous end joining ,Gene Targeting ,Mutation ,Biotechnology - Abstract
Light stimulates carotenoid production in an oleaginous yeast Rhodosporidium toruloides NBRC 10032 by promoting carotenoid biosynthesis genes. These genes undergo two-step transcriptional activation. The potential light regulator, Cryptochrome DASH (CRY1), has been suggested to contribute to this mechanism. In this study, based on KU70 (a component of nonhomologous end joining (NHEJ)) disrupting background, CRY1 disruptant was constructed to clarify CRY1 function. From analysis of CRY1 disruptant, it was suggested that CRY1 has the activation role of the carotenogenic gene expression. To obtain further insights into the light response, mutants varying carotenoid production were generated. Through analysis of mutants, the existence of the control two-step gene activation was proposed. In addition, our data analysis showed the strong possibility that R. toruloides NBRC 10032 is a homo-diploid strain.
- Published
- 2021
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