作者: Mayuko Adachi , Kunio Itoh , Akiko Masubuchi , Nobuaki Watanabe , Yorihisa Tanaka
DOI: 10.5483/BMBREP.2007.40.6.1021
关键词:
摘要: We demonstrated the genetic polymorphism of aldehyde oxidase (AO) in Donryu strain rats: ultrarapid metabolizer (UM) with nucleotide mutation (377G, 2604C) coding for amino acid substitution (110Gly, 852Val), extensive (EM) (377G/A, 2604C/T) (110Gly/Ser, 852Val/Ala), and poor (PM) (377A, 2604T) (110Ser, 852Ala), respectively. The results suggested that 377G > A and/or 2604C T should be responsible polymorphism. In this study, we constructed an E. coli expression system four types AO cDNA including Mut-1 Mut-2 as well naturally existing sequences UM PM order to clarify which one is showed almost same high low activity groups, Thus, study mutant directly revealed A, but not T, will play a critical role rats. reason cause was discussed.