TY - JOUR
T1 - Tryptophanase gene deficiency improves the application of dioxygenase to 3-(2-hydroxyethyl)catechol production
AU - Matsude, Megumi
AU - Okamoto, Himeka
AU - Aono, Riku
AU - Kino, Kuniki
N1 - Funding Information:
We would like to thank Mr. Daisuke Tateiwa (Nippon Shokubai Co., Osaka, Japan) for kindly supplying 3-(2-hydroxyethyl)catechol. This work was supported by the Japan Society for the Promotion of Science [JSPS KAKENHI 18H01802 to K.K.].
Funding Information:
We would like to thank Mr. Daisuke Tateiwa (Nippon Shokubai Co. Osaka, Japan) for kindly supplying 3-(2-hydroxyethyl)catechol. This work was supported by the Japan Society for the Promotion of Science [JSPS KAKENHI 18H01802 to K.K.].
Publisher Copyright:
© 2021 The Society for Biotechnology, Japan
PY - 2021/9
Y1 - 2021/9
N2 - 3-(2-Hydroxyethyl)catechol (HEC) is a polyphenol reported to exhibit skin-lightning and antioxidative effects, and hence is expected to be used as cosmetic and food additives and chemical products such as electronic materials. In this study, we established biocatalytic HEC production from 2-phenylethanol using the dioxygenase whose expression was induced by toluene, CumA, and its flanking dehydrogenase, CumB, from an isolated strain, Pseudomonas sp. K17. Escherichia coli cells coexpressing CumA and CumB were stained blue during cultivation in Luria–Bertani medium, and HEC was not produced upon using the cell-free extracts as biocatalysts, likely resulting from the inhibitory effects of the blue dyes. The disruption of the tryptophanase gene of E. coli was found to repress the generation of the blue dyes, and enhanced HEC production. The blue dyes were extracted from the cell-free extracts, and their molecular formula was C16H10N2O3, suggesting they were monooxygenated indigo or its isomers. Although repression of blue dye formation and enhancement of HEC production were observed when cells were cultivated with glucose, the percent yield of HEC was 84% at 20 h, whereas that with tryptophanase disruption strain was 84% at 4 h. It was suggested that tryptophanase gene disruption could contribute to more efficient HEC production.
AB - 3-(2-Hydroxyethyl)catechol (HEC) is a polyphenol reported to exhibit skin-lightning and antioxidative effects, and hence is expected to be used as cosmetic and food additives and chemical products such as electronic materials. In this study, we established biocatalytic HEC production from 2-phenylethanol using the dioxygenase whose expression was induced by toluene, CumA, and its flanking dehydrogenase, CumB, from an isolated strain, Pseudomonas sp. K17. Escherichia coli cells coexpressing CumA and CumB were stained blue during cultivation in Luria–Bertani medium, and HEC was not produced upon using the cell-free extracts as biocatalysts, likely resulting from the inhibitory effects of the blue dyes. The disruption of the tryptophanase gene of E. coli was found to repress the generation of the blue dyes, and enhanced HEC production. The blue dyes were extracted from the cell-free extracts, and their molecular formula was C16H10N2O3, suggesting they were monooxygenated indigo or its isomers. Although repression of blue dye formation and enhancement of HEC production were observed when cells were cultivated with glucose, the percent yield of HEC was 84% at 20 h, whereas that with tryptophanase disruption strain was 84% at 4 h. It was suggested that tryptophanase gene disruption could contribute to more efficient HEC production.
KW - 3-(2-Hydroxyethyl)catechol
KW - Dehydrogenase
KW - Dioxygenase
KW - Gene disruption
KW - Tryptophanase
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U2 - 10.1016/j.jbiosc.2021.06.001
DO - 10.1016/j.jbiosc.2021.06.001
M3 - Article
C2 - 34167862
AN - SCOPUS:85109413160
SN - 1389-1723
VL - 132
SP - 241
EP - 246
JO - Journal of Bioscience and Bioengineering
JF - Journal of Bioscience and Bioengineering
IS - 3
ER -