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A large-scale metagenomic study for enzyme profiles using the focused identification of the NGS-based definitive enzyme research (FINDER) strategy.
Sung, Jae-Yoon; Lee, Yong-Jik; Cho, Yong-Joon; Shin, Myeong-Na; Lee, Sang-Jae; Lee, Han-Seung; Koh, Hong; Bae, Jin-Woo; Shin, Jae-Ho; Kim, Hyun Jung; Lee, Dong-Woo.
Afiliação
  • Sung JY; Department of Biotechnology, Yonsei University, Seoul, South Korea.
  • Lee YJ; Department of Bio-Cosmetics, Seowon University, Chung-Ju, South Korea.
  • Cho YJ; Department of Biological Sciences and Research Institute of Basic Sciences, Seoul National University, Seoul, South Korea.
  • Shin MN; Department of Central Area Crop Science, NICS, RDA, Suwon, South Korea.
  • Lee SJ; Major in Food Biotechnology, Silla University, Busan, South Korea.
  • Lee HS; Major in Food Biotechnology, Silla University, Busan, South Korea.
  • Koh H; Department of Pediatrics, Yonsei University, Seoul, South Korea.
  • Bae JW; Department of Biology, Kyung Hee University, Seoul, South Korea.
  • Shin JH; Department of Applied Biosciences, Kyungpook National University, Daegu, South Korea.
  • Kim HJ; Department of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, USA.
  • Lee DW; Department of Biotechnology, Yonsei University, Seoul, South Korea.
Biotechnol Bioeng ; 118(11): 4360-4374, 2021 11.
Article em En | MEDLINE | ID: mdl-34309016
ABSTRACT
Excavating the molecular details of many diverse enzymes from metagenomes remains challenging in agriculture, food, health, and environmental fields. We present a versatile method that accelerates metabolic enzyme discovery for highly selective gene capture in metagenomes using next-generation sequencing. Culture-independent enzyme mining of environmental DNA is based on a set of short identifying degenerate sequences specific for a wide range of enzyme superfamilies, followed by multiplexed DNA barcode sequencing. A strategy of 'focused identification of next-generation sequencing-based definitive enzyme research' enabled us to generate targeted enzyme datasets from metagenomes, resulting in minimal hands-on obtention of high-throughput biological diversity and potential function profiles, without being time-consuming. This method also provided a targeted inventory of predicted proteins and molecular features of metabolic activities from several metagenomic samples. We suggest that the efficiency and sensitivity of this method will accelerate the decryption of microbial diversity and the signature of proteins and their metabolism from environmental samples.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Enzimas / Metagenômica / Código de Barras de DNA Taxonômico / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Enzimas / Metagenômica / Código de Barras de DNA Taxonômico / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article