Identification of enzymes from genus Trichoderma that can accelerate formation of ferulic acid and ethyl ferulate in collaboration with rice koji enzyme in sake mash

التفاصيل البيبلوغرافية
العنوان: Identification of enzymes from genus Trichoderma that can accelerate formation of ferulic acid and ethyl ferulate in collaboration with rice koji enzyme in sake mash
المؤلفون: Koji Noge, Kouto Takano, Itsuki Takahashi, Masaki Okuda, Anna Sato, Katsumi Hashizume, Takahito Ito, Toshihiko Ito
المصدر: Journal of Bioscience and Bioengineering. 128:177-182
بيانات النشر: Elsevier BV, 2019.
سنة النشر: 2019
مصطلحات موضوعية: 0106 biological sciences, 0301 basic medicine, Coumaric Acids, Bioengineering, Cellulase, 01 natural sciences, Applied Microbiology and Biotechnology, Ferulic acid, 03 medical and health sciences, chemistry.chemical_compound, Caffeic Acids, 010608 biotechnology, Arabinoxylan, Glycoside hydrolase family 10, Food science, Trichoderma, chemistry.chemical_classification, biology, Alcoholic Beverages, food and beverages, Oryza, Enzyme assay, Kinetics, 030104 developmental biology, Enzyme, chemistry, biology.protein, Xylanase, Xylans, Fermentation, Biotechnology
الوصف: The enzymes responsible for acceleration of ferulic acid and ethyl ferulate formation in sake mash were studied. Ferulic acid and ethyl ferulate are formed during the sake brewing process from feruloylated glucuronoarabinoxylan. Cellulase reagent from genus Trichoderma was used instead of rice koji, because rice koji for sake brewing produces extremely low levels of xylan-degrading enzymes. A combination of the reagent with rice koji enzymes accelerated the formation of ferulic acid from α-rice powder. Addition of the reagent to sake mash increased ferulic acid and ethyl ferulate formation. The enzyme responsible for the accelerated formation was purified using a newly developed assay method and α-rice powder as a substrate. During the assay procedure, feruloylated oligosaccharide was converted to ferulic acid by feruloylesterase for HPLC analysis. Analysis of the N-terminal amino acid sequence of the purified samples was successfully conducted after pyroglutamyl aminopeptidase de-blocking. Purified enzymes were identified as members of the glycoside hydrolase family 10 (GH10) and family 11 (GH11) xylanases by BLASTP database research. The GH10 xylanase showed higher specific activity for α-rice powder and insoluble wheat arabinoxylan compared with GH11 xylanase; the GH11 xylanase showed higher specific activity for the other xylan substrates, especially glucuronoarabinoxylan. The GH10 xylanase showed higher accelerating activity than the GH11 xylanase in the sake mash. The results of this study provides useful knowledge on ferulic acid and ethyl ferulate formation in sake mash, the relative levels of these compounds and their influence on the sensory quality of sake.
تدمد: 1389-1723
DOI: 10.1016/j.jbiosc.2019.01.014
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0959cf99e9183dc4e1116327e6116ca5
https://doi.org/10.1016/j.jbiosc.2019.01.014
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....0959cf99e9183dc4e1116327e6116ca5
قاعدة البيانات: OpenAIRE
الوصف
تدمد:13891723
DOI:10.1016/j.jbiosc.2019.01.014