Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme gene

AbstractHigher alcohols are not only the key flavor substance but also the precursor of other flavor substances in Baijiu. In the metabolic pathway of higher alcohols, alcohol dehydrogenase (ADH) plays an important role and its genes can be used as a marker gene for analyzing the producer of higher...

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Main Authors: Mandlaa, Yuting Ren, Meiling Qiao, Yuzhen Yang, Guojun Ren, Zhongjun Chen, Ziyu Sun
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Cogent Food & Agriculture
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/23311932.2024.2306014
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author Mandlaa
Yuting Ren
Meiling Qiao
Yuzhen Yang
Guojun Ren
Zhongjun Chen
Ziyu Sun
author_facet Mandlaa
Yuting Ren
Meiling Qiao
Yuzhen Yang
Guojun Ren
Zhongjun Chen
Ziyu Sun
author_sort Mandlaa
collection DOAJ
description AbstractHigher alcohols are not only the key flavor substance but also the precursor of other flavor substances in Baijiu. In the metabolic pathway of higher alcohols, alcohol dehydrogenase (ADH) plays an important role and its genes can be used as a marker gene for analyzing the producer of higher alcohols. In this study, the degenerate primers of Zinc-dependent long-chain ADH gene (L.adh) were designed and applied to investigate the diversity of L.adh in different Daqu (HT, SC and SD). The results showed that the degenerate primers were able to amplify the fragment of L.adh and had good coverage in high-throughput sequencing. The diversity and composition of L.adh in the three kinds of Daqu were different and the diversity of L.adh in SC was the highest while HT was the lowest. The predominant L.adh in SC and HT were form Bacillus (54%–78%) and Aspergillus (64%–66%), respectively, and the predominant L.adh in SD were from Aspergillus (7%–51%) and Enterobacter (2%–47%). In addition, L.adh from bacteria and fungi could be clustered into one evolutionary branch and divided into 10 clusters. The findings of this study will provide a new perspective for evaluating the potential microorganisms associated with higher alcohol synthesis in Daqu and reference for selecting suitable Daqu in the production of Baijiu.
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spelling doaj.art-70f160ede2e045eca5abb7e13573ec272024-01-27T12:16:51ZengTaylor & Francis GroupCogent Food & Agriculture2331-19322024-12-0110110.1080/23311932.2024.2306014Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme geneMandlaa0Yuting Ren1Meiling Qiao2Yuzhen Yang3Guojun Ren4Zhongjun Chen5Ziyu Sun6College of Food Science and Engineering, Inner Mongolia Agricultural University, Hohhot, ChinaCollege of Food Science and Engineering, Inner Mongolia Agricultural University, Hohhot, ChinaCollege of Food Science and Engineering, Inner Mongolia Agricultural University, Hohhot, ChinaInner Mongolia Hetao Liquor Group Co., Ltd, Bayannur, ChinaInner Mongolia Hetao Liquor Group Co., Ltd, Bayannur, ChinaCollege of Food Science and Engineering, Inner Mongolia Agricultural University, Hohhot, ChinaCollege of Food Science and Engineering, Inner Mongolia Agricultural University, Hohhot, ChinaAbstractHigher alcohols are not only the key flavor substance but also the precursor of other flavor substances in Baijiu. In the metabolic pathway of higher alcohols, alcohol dehydrogenase (ADH) plays an important role and its genes can be used as a marker gene for analyzing the producer of higher alcohols. In this study, the degenerate primers of Zinc-dependent long-chain ADH gene (L.adh) were designed and applied to investigate the diversity of L.adh in different Daqu (HT, SC and SD). The results showed that the degenerate primers were able to amplify the fragment of L.adh and had good coverage in high-throughput sequencing. The diversity and composition of L.adh in the three kinds of Daqu were different and the diversity of L.adh in SC was the highest while HT was the lowest. The predominant L.adh in SC and HT were form Bacillus (54%–78%) and Aspergillus (64%–66%), respectively, and the predominant L.adh in SD were from Aspergillus (7%–51%) and Enterobacter (2%–47%). In addition, L.adh from bacteria and fungi could be clustered into one evolutionary branch and divided into 10 clusters. The findings of this study will provide a new perspective for evaluating the potential microorganisms associated with higher alcohol synthesis in Daqu and reference for selecting suitable Daqu in the production of Baijiu.https://www.tandfonline.com/doi/10.1080/23311932.2024.2306014Higher alcoholalcohol dehydrogenasediversityBaijiufunctional geneM. Luisa Escudero-Gilete, Universidad de Sevilla, Spain
spellingShingle Mandlaa
Yuting Ren
Meiling Qiao
Yuzhen Yang
Guojun Ren
Zhongjun Chen
Ziyu Sun
Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme gene
Cogent Food & Agriculture
Higher alcohol
alcohol dehydrogenase
diversity
Baijiu
functional gene
M. Luisa Escudero-Gilete, Universidad de Sevilla, Spain
title Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme gene
title_full Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme gene
title_fullStr Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme gene
title_full_unstemmed Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme gene
title_short Profiling the potential producers of higher alcohol in different Daqu (a starter of Baijiu) by amplifying the key enzyme gene
title_sort profiling the potential producers of higher alcohol in different daqu a starter of baijiu by amplifying the key enzyme gene
topic Higher alcohol
alcohol dehydrogenase
diversity
Baijiu
functional gene
M. Luisa Escudero-Gilete, Universidad de Sevilla, Spain
url https://www.tandfonline.com/doi/10.1080/23311932.2024.2306014
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