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Cloning,sequencing and expression analysis of a gene encoding alcohol oxidase in Paenibacillus sp. AIU 311
Authors:Yasutaka Sasaki  Michihiko Kataoka  Nobuyuki Urano  Jun Ogawa  Akira Iwasaki  Junzo Hasegawa  Kimiyasu Isobe  Sakayu Shimizu
Affiliation:1 The United Graduate School of Agricultural Sciences, Iwate University, 18-8, Ueda 3-chome, Morioka 020-8550, Japan;2 Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan;3 Life Science R & D Center, Kaneka Co., Miyamae-machi, Takasaga-cho, Takasago 676-8688, Japan
Abstract:We have cloned a gene encoding an alcohol oxidase (AOD) specific to aldehyde alcohols from Paenibacillus sp. AIU 311. The AOD gene contains an open reading frame consisting of 618 nucleotides corresponding to 205 amino acid residues. The deduced amino acid sequence exhibits a high similarity to that of manganese superoxide dismutases (SODs). We expressed the cloned gene as an active product in Escherichia coli BL21 cells. The productivity (total units per culture broth volume) of the recombinant AOD expressed in E. coli BL21 is 26,000-fold higher than that of AOD in Paenibacillus sp. AIU 311. The recombinant AOD also exhibits aldehyde alcohol oxidase activity and SOD activity. The recombinant cells described in this study have utility for the production of glyoxal from glycolaldehyde.
Keywords:Glycolaldehyde   Glyoxal   Aldehyde alcohol   Alcohol oxidase   Superoxide dismutase   Paenibacillus sp.
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