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6-Deoxyhexoses from l-Rhamnose in the Search for Inducers of the Rhamnose Operon: Synergy of Chemistry and Biotechnology.
Liu, Zilei; Yoshihara, Akihide; Kelly, Ciarán; Heap, John T; Marqvorsen, Mikkel H S; Jenkinson, Sarah F; Wormald, Mark R; Otero, José M; Estévez, Amalia; Kato, Atsushi; Fleet, George W J; Estévez, Ramón J; Izumori, Ken.
  • Liu Z; Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford, OX1 3TA, UK.
  • Yoshihara A; Glycobiology Institute, Department of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
  • Kelly C; International Institute of Rare Sugar Research and Education, Kagawa University, Miki, Kagawa, 761-0795, Japan. yoshihara@ag.kagawa-u.ac.jp.
  • Heap JT; Centre for Synthetic Biology and Innovation, Department of Life Sciences, Imperial College, London, SW7 2AZ, UK.
  • Marqvorsen MH; Centre for Synthetic Biology and Innovation, Department of Life Sciences, Imperial College, London, SW7 2AZ, UK.
  • Jenkinson SF; Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford, OX1 3TA, UK.
  • Wormald MR; Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford, OX1 3TA, UK.
  • Otero JM; Glycobiology Institute, Department of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
  • Estévez A; Departamento de Química Orgánica and Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares, Universidade de Santiago de Compostela, 15782, Santiago de Compostela, Spain.
  • Kato A; Departamento de Química Orgánica and Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares, Universidade de Santiago de Compostela, 15782, Santiago de Compostela, Spain.
  • Fleet GW; Department of Hospital Pharmacy, University of Toyama, Toyama, 930-0194, Japan.
  • Estévez RJ; Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford, OX1 3TA, UK. george.fleet@chem.ox.ac.uk.
  • Izumori K; Departamento de Química Orgánica and Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares, Universidade de Santiago de Compostela, 15782, Santiago de Compostela, Spain. ramon.estevez@usc.es.
Chemistry ; 22(35): 12557-65, 2016 Aug 22.
Article en En | MEDLINE | ID: mdl-27439720
ABSTRACT
In the search for alternative non-metabolizable inducers in the l-rhamnose promoter system, the synthesis of fifteen 6-deoxyhexoses from l-rhamnose demonstrates the value of synergy between biotechnology and chemistry. The readily available 2,3-acetonide of rhamnonolactone allows inversion of configuration at C4 and/or C5 of rhamnose to give 6-deoxy-d-allose, 6-deoxy-d-gulose and 6-deoxy-l-talose. Highly crystalline 3,5-benzylidene rhamnonolactone gives easy access to l-quinovose (6-deoxy-l-glucose), l-olivose and rhamnose analogue with C2 azido, amino and acetamido substituents. Electrophilic fluorination of rhamnal gives a mixture of 2-deoxy-2-fluoro-l-rhamnose and 2-deoxy-2-fluoro-l-quinovose. Biotechnology provides access to 6-deoxy-l-altrose and 1-deoxy-l-fructose.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ramnosa / Desoxiazúcares / Desoxiglucosa / Fructosa / Glucosa / Hexosas Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ramnosa / Desoxiazúcares / Desoxiglucosa / Fructosa / Glucosa / Hexosas Idioma: En Año: 2016 Tipo del documento: Article