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Assay for okadaic acid O-acyl transferase using HPLC-FLD.
Terauchi, Masato; Komazaki, Yuki; Yoshino, Atsushi; Cho, Yuko; Kudo, Yuta; Yotsu-Yamashita, Mari; Konoki, Keiichi.
Afiliação
  • Terauchi M; Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan.
  • Komazaki Y; Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan.
  • Yoshino A; Tropical Technology Plus, Okinawa, Japan.
  • Cho Y; Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan.
  • Kudo Y; Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan.
  • Yotsu-Yamashita M; Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai, Miyagi, Japan.
  • Konoki K; Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan.
Biosci Biotechnol Biochem ; 88(9): 999-1006, 2024 Aug 26.
Article em En | MEDLINE | ID: mdl-38886126
ABSTRACT
Dinophysistoxin 1 (DTX1, 1) and okadaic acid (OA, 2), produced by the dinoflagellates Dinophysis spp. and Prorocentrum spp., are primary diarrhetic shellfish toxins (DSTs), which may cause gastric illness in people consuming such as bivalves. Both compounds convert to dinophysistoxin 3 (DTX3, 3; generic name for 1 and 2 with fatty acids conjugated at 7-OH) in bivalves. The enzyme okadaic acid O-acyl transferase (OOAT) is a membrane protein found in the microsomes of the digestive glands of bivalves. In this study, we established an in vitro enzymatic conversion reaction using 4-nitro-2,1,3-benzoxadiazole (NBD)-OA (4), an OA derivative conjugated with (R)-(-)-4-nitro-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole (NBD-APy) on 1-CO2H, as a substrate. We detected the enzymatically produced 3, NBD-7-O-palmitoyl-OA (NBD-Pal-OA), using high-performance liquid chromatography-fluorescence detection. We believe that an OOAT assay using 4 will facilitate the fractionation and isolation of OOAT in the future.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aciltransferases / Ácido Okadáico Limite: Animals Idioma: En Revista: Biosci Biotechnol Biochem Assunto da revista: BIOQUIMICA / BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aciltransferases / Ácido Okadáico Limite: Animals Idioma: En Revista: Biosci Biotechnol Biochem Assunto da revista: BIOQUIMICA / BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão