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Catalytic residues, substrate specificity, and role in carbon starvation of the 2-hydroxy FA dioxygenase Mpo1 in yeast
| Title: | Catalytic residues, substrate specificity, and role in carbon starvation of the 2-hydroxy FA dioxygenase Mpo1 in yeast |
| Authors: | Mori, Keisuke Browse this author | | Obara, Takashi Browse this author | | Seki, Naoya Browse this author | | Miyamoto, Masatoshi Browse this author | | Naganuma, Tatsuro Browse this author | | Kitamura, Takuya Browse this author | | Kihara, Akio Browse this author →KAKEN DB |
| Keywords: | ceramides | | fatty acid | | oxidation | | 2-hydroxy fatty acid | | iron | | lipids | | alpha-oxidation | | sphingolipids |
| Issue Date: | Jul-2020 |
| Publisher: | American Society for Biochemistry and Molecular Biology (ASBMB) |
| Journal Title: | Journal of Lipid Research (JLR) |
| Volume: | 61 |
| Issue: | 7 |
| Start Page: | 1104 |
| End Page: | 1114 |
| Publisher DOI: | 10.1194/jlr.RA120000803 |
| Abstract: | The yeast protein Mpo1 belongs to a protein family that is widely conserved in bacteria, fungi, protozoa, and plants, and is the only protein of this family whose function has so far been elucidated. Mpo1 is an Fe2+-dependent dioxygenase that catalyzes the alpha-oxidation reaction of 2-hydroxy (2-OH) long-chain FAs (LCFAs) produced in the degradation pathway of the long-chain base phytosphingosine. However, several biochemical characteristics of Mpo1, such as its catalytic residues, membrane topology, and substrate specificity, remain unclear. Here, we report that yeast Mpo1 contains two transmembrane domains and that both its N- and C-terminal regions are exposed to the cytosol. Mutational analyses revealed that three histidine residues conserved in the Mpo1 family are especially important for Mpo1 activity, suggesting that they may be responsible for the formation of coordinate bonds with Fe2+. We found that, in addition to activity toward 2-OH LCFAs, Mpo1 also exhibits activity toward 2-OH very-long-chain FAs derived from the FA moiety of sphingolipids. These results indicate that Mpo1 is involved in the metabolism of long-chain to very-long-chain 2-OH FAs produced in different pathways. We noted that the growth ofmpo1 Delta cells is delayed upon carbon deprivation, suggesting that the Mpo1-mediated conversion of 2-OH FAs to nonhydroxy FAs is important for utilizing 2-OH FAs as a carbon source under carbon starvation. Our findings help to elucidate the as yet unknown functions and activities of other Mpo1 family members. |
| Rights: | This research was originally published in the Journal of Lipid Research. Mori, Keisuke et al. Catalytic residues, substrate specificity, and role in carbon starvation of the 2-hydroxy FA dioxygenase Mpo1 in yeast. Journal of Lipid Research. 2020; 61:1104-1114. © the American Society for Biochemistry and Molecular Biology. |
| Type: | article |
| URI: | http://hdl.handle.net/2115/82334 |
| Appears in Collections: | 薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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Submitter: 木原 章雄
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