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      Identification of two highly promiscuous thermostable sugar nucleotidylyltransferases for glycorandomization

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      https://www.riss.kr/link?id=O119168731

      • 저자
      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2018년

      • 작성언어

        -

      • Print ISSN

        1742-464X

      • Online ISSN

        1742-4658

      • 등재정보

        SCI;SCIE;SCOPUS

      • 자료형태

        학술저널

      • 수록면

        2840-2855   [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]

      • 구독기관
        • 전북대학교 중앙도서관  
        • 성균관대학교 중앙학술정보관  
        • 부산대학교 중앙도서관  
        • 전남대학교 중앙도서관  
        • 제주대학교 중앙도서관  
        • 중앙대학교 서울캠퍼스 중앙도서관  
        • 인천대학교 학산도서관  
        • 숙명여자대학교 중앙도서관  
        • 서강대학교 로욜라중앙도서관  
        • 계명대학교 동산도서관  
        • 충남대학교 중앙도서관  
        • 한양대학교 백남학술정보관  
        • 이화여자대학교 중앙도서관  
        • 고려대학교 도서관  
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      부가정보

      다국어 초록 (Multilingual Abstract)

      Glycorandomization is a process that improves the efficacy of glycoconjugates by the addition of a diverse array of sugars to secondary metabolites and antibiotics of pharmaceutical importance. This process, which employs sugar nucleotidylyltransferases (SNTs) and glycosyl transferases (GTs) in tandem, would benefit by the employment of promiscuous enzymes, i.e. those with the ability to utilize diverse noncanonical substrates. As promiscuous GTs are available, here we set out to identify promiscuous SNTs. For this, we began with a detailed family‐wide characterization of SNTs. Earlier, we had proposed that SNTs could be classified into two major groups – I and II. They share a common structural framework and utilize a similar catalytic mechanism. Subtle variations in the way two magnesium ions — MgA2+ and MgB2+ — are stabilized by metal ion coordination motifs led to their classification into diverse subgroups viz. I‐A, I‐B, I‐C, II‐A, and II‐B. Based on this classification, here we investigate promiscuity across the entire family of SNTs. We study the utilization of several sugar phosphates and nucleotides by the various subgroups of SNTs to understand substrate specificity and promiscuity in these. We find that promiscuity is prevalent among SNTs; and in particular, in the thermophilic homologs. In principle, promiscuity profiling identified four new SNTs that can be employed for the production of sugar‐nucleotide libraries. However, assaying for their ability to simultaneously utilize multiple substrates in a single‐pot reaction, we find two thermophilic SNTs‐ TMGA, an adenylyltransferase from Thermotoga maritima and PHGT, a thymidylyltransferase from Pyrococcus horikoshii that are readily employable for the production of diverse sugar‐nucleotides.
      Family‐wide promiscuity analysis of sugar nucleotidylyltransferases: SNTs can be classified into five groups, based on structural motifs. Probing each group of SNTs for prevalence of substrate promiscuity, we identified two potential candidates. The combination of PHGT, a thymidylyltransferase from Pyrococcus horikoshii and TMGA, an adenylyltransferase from Thermotoga maritima can be employed for the production of sugar‐nucleotide libraries in a single pot reaction.
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      Glycorandomization is a process that improves the efficacy of glycoconjugates by the addition of a diverse array of sugars to secondary metabolites and antibiotics of pharmaceutical importance. This process, which employs sugar nucleotidylyltransferas...

      Glycorandomization is a process that improves the efficacy of glycoconjugates by the addition of a diverse array of sugars to secondary metabolites and antibiotics of pharmaceutical importance. This process, which employs sugar nucleotidylyltransferases (SNTs) and glycosyl transferases (GTs) in tandem, would benefit by the employment of promiscuous enzymes, i.e. those with the ability to utilize diverse noncanonical substrates. As promiscuous GTs are available, here we set out to identify promiscuous SNTs. For this, we began with a detailed family‐wide characterization of SNTs. Earlier, we had proposed that SNTs could be classified into two major groups – I and II. They share a common structural framework and utilize a similar catalytic mechanism. Subtle variations in the way two magnesium ions — MgA2+ and MgB2+ — are stabilized by metal ion coordination motifs led to their classification into diverse subgroups viz. I‐A, I‐B, I‐C, II‐A, and II‐B. Based on this classification, here we investigate promiscuity across the entire family of SNTs. We study the utilization of several sugar phosphates and nucleotides by the various subgroups of SNTs to understand substrate specificity and promiscuity in these. We find that promiscuity is prevalent among SNTs; and in particular, in the thermophilic homologs. In principle, promiscuity profiling identified four new SNTs that can be employed for the production of sugar‐nucleotide libraries. However, assaying for their ability to simultaneously utilize multiple substrates in a single‐pot reaction, we find two thermophilic SNTs‐ TMGA, an adenylyltransferase from Thermotoga maritima and PHGT, a thymidylyltransferase from Pyrococcus horikoshii that are readily employable for the production of diverse sugar‐nucleotides.
      Family‐wide promiscuity analysis of sugar nucleotidylyltransferases: SNTs can be classified into five groups, based on structural motifs. Probing each group of SNTs for prevalence of substrate promiscuity, we identified two potential candidates. The combination of PHGT, a thymidylyltransferase from Pyrococcus horikoshii and TMGA, an adenylyltransferase from Thermotoga maritima can be employed for the production of sugar‐nucleotide libraries in a single pot reaction.

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