Taichi Takasuka
Associate Professor
Research Interests
Explore related searches
Contact this professor
Get a free first email built on one of their papers, ready for you to edit and send yourself.
About
Taichi Takasuka is an Associate Professor at Hokkaido University in Japan. His research primarily focuses on plant biology, including the characterization of aminotransferases and the role of extracellular vesicles in cartilage. Additionally, he investigates the biochemical properties of fungal enzymes and the bioprocessing of plant biomass. His recent publications reflect a commitment to understanding the molecular mechanisms underlying plant and fungal interactions.
Articles (16)
Year:
2025
White-rot fungi, such as Phanerochaete chrysosporium , are the most efficient degraders of lignin, a major component of plant biomass. Enzymes produced by these fungi, such as lignin peroxidases and manganese peroxidases, break down lignin polymers into various aromatic compounds based on guaiacyl, syringyl, and hydroxyphenyl units. These intermediates are further degraded, and the aromatic ring is cleaved by 1,2,4-trihydroxybenzene dioxygenases. This study aimed to characterize homogentisate dioxygenase (HGD)-like proteins from P. chrysosporium that are strongly induced by the G-unit fragment of vanillin. We overexpressed two homologous recombinant HGDs, PcHGD1 and PcHGD2, in Escherichia coli . Both PcHGD1 and PcHGD2 catalyzed the ring cleavage in methoxyhydroquinone (MHQ) and dimethoxyhydroquinone (DMHQ). The two enzymes had the highest catalytic efficiency ( k cat / K m ) for MHQ, and therefore, we named PcHGD1 and PcHGD2 as MHQ dioxygenases 1 and 2 (PcMHQD1 and PcMHQD2), respectively, from P. chrysosporium . This is the first study to identify and characterize MHQ and DMHQ dioxygenase activities in members of the HGD superfamily. These findings highlight the unique and broad substrate spectra of PcHGDs, rendering them attractive candidates for biotechnological applications. IMPORTANCE This study aimed to elucidate the properties of enzymes responsible for degrading lignin, a dominant natural polymer in terrestrial lignocellulosic biomass. We focused on two homogentisate dioxygenase (HGD) homologs from the white-rot fungus, P. chrysosporium , and investigated their roles in the degradation of lignin-derived aromatic compounds. In the P. chrysosporium genome database, PcMHQD1 and PcMHQD2 were annotated as HGDs that could cleave the aromatic rings of methoxyhydroquinone (MHQ) and dimethoxyhydroquinone (DMHQ) with a preference for MHQ. These findings suggest that MHQD1 and/or MHQD2 play important roles in the degradation of lignin-derived aromatic compounds by P. chrysosporium . The preference of PcMHQDs for MHQ and DMHQ not only highlights their potential for biotechnological applications but also underscores their critical role in understanding lignin degradation by a representative of white-rot fungus, P. chrysosporium .
Year:
2024
Year:
2024
Year:
2024
Year:
2023
Year:
2023
Year:
2023
Year:
2023
Year:
2023
Year:
2022
Year:
2021
Year:
2021
Year:
2021
Year:
2021
Year:
2021
Year:
2020
Collaborators (13)
Junpei Takano
Professor
Osaka University
Marcel Beier
Assistant Professor
Hokkaido University
Rohinton Kamakaka
Professor
University of California, Santa Cruz
Akira Yoshinari
YLC Assistant Professor
Nagoya University
Brian G. Fox
-
Alaa Terkawi
Assistant Professor
Hokkaido University
Taku Ebata
Hokkaido University
Akira Kakugo
Hokkaido University
Chiaki Hori
Associate Professor
Hokkaido University
Samuel Deutsch
Chief Scientific Officer
Denali Therapeutics
Daisuke Inoue
Assistant Professor
Kyushu University
Motoyuki Shimizu
Meijo University
Yoichiro Fukao
-
Make your next move.
Prepare your application
Review drafts before you send them.