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      SCIE SCOPUS KCI등재

      Molecular Cloning and Characterization of a Novel Cold-Adapted Family VIII Esterase from a Biogas Slurry Metagenomic Library = Molecular Cloning and Characterization of a Novel Cold-Adapted Family VIII Esterase from a Biogas Slurry Metagenomic Library

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      https://www.riss.kr/link?id=A100177618

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      다국어 초록 (Multilingual Abstract)

      A novel esterase gene, est01, was successfully unearthed from a biogas digester microbiota metagenomic library. The 1,194 bp est01 gene encodes a protein of 44,804 Da (designated Est01). The amino acid sequence of Est01 shows only moderate (33%) identity to a lipase/ esterase. Phylogenetic analysis and biochemical characterization confirmed that Est01 is a new member of family VIII esterases. The purified Est01 from recombinant Escherichia coli BL21 (DE3) showed high hydrolytic activity against short-chain fatty acid esters, suggesting that it is a typical carboxylesterase rather than a lipase. Furthermore, the Est01 was even active at 10°C (43% activity remained), with the optimal temperature at 20°C, and had a broad pH range from 5.0 to 10.0, with the optimal pH of 8.0. These properties suggest that Est01 is a cold-adaptive esterase and could have good potential for low-temperature hydrolysis application.
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      A novel esterase gene, est01, was successfully unearthed from a biogas digester microbiota metagenomic library. The 1,194 bp est01 gene encodes a protein of 44,804 Da (designated Est01). The amino acid sequence of Est01 shows only moderate (33%) ident...

      A novel esterase gene, est01, was successfully unearthed from a biogas digester microbiota metagenomic library. The 1,194 bp est01 gene encodes a protein of 44,804 Da (designated Est01). The amino acid sequence of Est01 shows only moderate (33%) identity to a lipase/ esterase. Phylogenetic analysis and biochemical characterization confirmed that Est01 is a new member of family VIII esterases. The purified Est01 from recombinant Escherichia coli BL21 (DE3) showed high hydrolytic activity against short-chain fatty acid esters, suggesting that it is a typical carboxylesterase rather than a lipase. Furthermore, the Est01 was even active at 10°C (43% activity remained), with the optimal temperature at 20°C, and had a broad pH range from 5.0 to 10.0, with the optimal pH of 8.0. These properties suggest that Est01 is a cold-adaptive esterase and could have good potential for low-temperature hydrolysis application.

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      참고문헌 (Reference)

      1 Finn RD, "The pfam protein families database" 36 : 281-288, 2008

      2 Joris B, "The active-site-serine penicillin-recognizing enzymes as members of the Streptomyces R61 DD-peptidase family" 250 : 313-324, 1988

      3 Cheng XJ, "Subtilase genes diversity in the biogas digester microbiota" 62 : 1542-1547, 2011

      4 Cheng XJ, "Screening of microbial community in biogas fermentation under low temperature and construction of its metagenome library" 30 : 50-55, 2010

      5 Knox JR, "Molecular evolution of bacterial β-lactam resistance" 3 : 937-947, 1996

      6 Kim YH, "Molecular cloning and characterization of a novel family viii alkaline esterase from a compost metagenomic library" 393 : 45-49, 2010

      7 Aurilia V, "Microbial carbohydrate esterases in cold adapted environments" 410 : 234-240, 2008

      8 Ellis EM., "Microbial aldo-keto reductases" 216 : 123-131, 2002

      9 Handelsman J., "Metagenomics: application of genomics to uncultured microorganisms" 68 : 669-685, 2004

      10 Tamura K, "MEGA4:molecular evolutionary genetics analysis (MEGA) software version 4.0" 24 : 1596-1599, 2007

      1 Finn RD, "The pfam protein families database" 36 : 281-288, 2008

      2 Joris B, "The active-site-serine penicillin-recognizing enzymes as members of the Streptomyces R61 DD-peptidase family" 250 : 313-324, 1988

      3 Cheng XJ, "Subtilase genes diversity in the biogas digester microbiota" 62 : 1542-1547, 2011

      4 Cheng XJ, "Screening of microbial community in biogas fermentation under low temperature and construction of its metagenome library" 30 : 50-55, 2010

      5 Knox JR, "Molecular evolution of bacterial β-lactam resistance" 3 : 937-947, 1996

      6 Kim YH, "Molecular cloning and characterization of a novel family viii alkaline esterase from a compost metagenomic library" 393 : 45-49, 2010

      7 Aurilia V, "Microbial carbohydrate esterases in cold adapted environments" 410 : 234-240, 2008

      8 Ellis EM., "Microbial aldo-keto reductases" 216 : 123-131, 2002

      9 Handelsman J., "Metagenomics: application of genomics to uncultured microorganisms" 68 : 669-685, 2004

      10 Tamura K, "MEGA4:molecular evolutionary genetics analysis (MEGA) software version 4.0" 24 : 1596-1599, 2007

      11 Ranjan R, "Isolation of novel lipolytic genes from uncultured bacteria of pond water" 335 : 57-65, 2005

      12 Roh C, "Isolation of a low-temperature adapted lipolytic enzyme from uncultivated microorganism" 105 : 116-123, 2008

      13 Elend C, "Isolation and biochemical characterization of two novel metagenome-derived esterases" 72 : 3637-3645, 2006

      14 Heath C, "Identification of a novel alkaliphilic esterase active at low temperatures by screening a metagenomic library from antarctic desert soil" 75 : 4657-4659, 2009

      15 Zhang T, "Gene cloning and characterization of a novel esterase from activated sludge metagenome" 8 : 67-, 2009

      16 Rhee SK, "Detection of genes involved in biodegradation and biotransformation in microbial communities by using 50-mer oligonucleotide microarrays" 70 : 4303-4317, 2004

      17 Larkin MA, "Clustal W and Clustal X version 2. 0" 23 : 2947-2948, 2007

      18 Laemmli UK, "Cleavage of structural proteins during the assembly of the head of bacteriophage T4" 227 : 680-685, 1970

      19 Arpigny JL, "Bacterial lipolytic enzymes:classification and properties" 343 : 177-183, 1999

      20 Steele HL, "Advances in recovery of novel biocatalysts from metagenomes" 16 : 25-37, 2009

      21 Bradford MM., "A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding" 72 : 248-254, 1976

      22 Hu XP, "A novel, extremely alkaliphilic and cold-active esterase from Antarctic desert soil" 16 : 79-86, 2012

      23 Rashamuse K, "A novel family VIII carboxylesterase derived from a leachate metagenome library exhibits promiscuous β-lactamase activity on nitrocefin" 83 : 491-500, 2009

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-04-04 학술지명변경 한글명 : -> Journal of Microbiology and Biotechnology KCI등재
      2006-03-30 학술지등록 한글명 :
      외국어명 : Journal of Microbiology and Biotechnology
      KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.59 0.33 1.17
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.91 0.78 0.472 0.08
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