2017 Fiscal Year Final Research Report
Characterization of biosynthetic pathways for the glycosylated mycosporine-like amino acids in the terrestrial cyanobacterium Nostoc commune.
Project/Area Number |
15K01799
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biomolecular chemistry
|
Research Institution | Kanazawa University |
Principal Investigator |
SAKAMOTO Toshio 金沢大学, 自然システム学系, 准教授 (70324069)
|
Co-Investigator(Kenkyū-buntansha) |
松郷 誠一 金沢大学, 自然システム学系, 教授 (30148126)
|
Research Collaborator |
SAKAMOTO Kaori 金沢工業大学, バイオ・化学部, 准教授 (10367443)
WADA Naoki 金沢大学, 理工研究域自然システム学系, 助教 (20464050)
|
Project Period (FY) |
2015-04-01 – 2018-03-31
|
Keywords | 多機能性分子 / 極限環境生物 / 抗酸化物質 / 紫外線 |
Outline of Final Research Achievements |
Mycosporine-like amino acids (MAAs) are water-soluble pigments that absorb UV radiation of 280 to 340 nm. The terrestrial cyanobacterium Nostoc commune is classified into four groups representing genetically different chemotypes by differences in their MAA derivatives. The mysABCD genes responsible for MAA biosynthesis were characterized in genotype A N. ccommune. The presence of the mysABCD gene cluster in N. commune strain KU002 supported its porphyra-334 producing capability via the Nostoc-type mechanism, although N. commune strain KU002 mainly produces the arabinose-bound derivative of porphyra-334. It can be postulated that N. commune additionally acquired the glycosylation of porphyra-334 to adapt to terrestrial environments. Further studies are necessary to elucidate the gene(s) involved in the glycosylation of porphyra-334.
|
Free Research Field |
植物生理生化学
|