ISSN: 2155-9872

Jornal de Técnicas Analíticas e Bioanalíticas

Acesso livre

Nosso grupo organiza mais de 3.000 Séries de conferências Eventos todos os anos nos EUA, Europa e outros países. Ásia com o apoio de mais 1.000 Sociedades e publica mais de 700 Acesso aberto Periódicos que contém mais de 50.000 personalidades eminentes, cientistas de renome como membros do conselho editorial.

Periódicos de acesso aberto ganhando mais leitores e citações
700 periódicos e 15 milhões de leitores Cada periódico está obtendo mais de 25.000 leitores

Indexado em
  • Índice de Fonte CAS (CASSI)
  • Índice Copérnico
  • Google Scholar
  • Sherpa Romeu
  • Banco de dados de revistas acadêmicas
  • Abra o portão J
  • Genâmica JournalSeek
  • JornalTOCs
  • PesquisaBíblia
  • Infraestrutura Nacional de Conhecimento da China (CNKI)
  • Diretório de Periódicos de Ulrich
  • Biblioteca de Periódicos Eletrônicos
  • RefSeek
  • Diretório de indexação de periódicos de pesquisa (DRJI)
  • Universidade Hamdard
  • EBSCO AZ
  • OCLC – WorldCat
  • Acadêmico
  • Catálogo online SWB
  • Biblioteca Virtual de Biologia (vifabio)
  • Publons
  • Euro Pub
  • ICMJE
Compartilhe esta página

Abstrato

Enzymatic Potential of Mucor inaequisporus for Naringin Biotransformation, Accessed by Fractional Factorial Design and Mass Spectrometry Analysis

Enzo Monte Canedo, Taicia Pacheco Fill, Edenir Rodrigues Pereira-Filho and Edson Rodrigues-Filho

Whole cells of Mucor inaequisporus were used for biotransformation of the flavonoid naringin, as a green method for structural diversification of this class of natural product. The metabolism of the fungus was challenged against naringin under several culturing conditions, using statistical optimization. Eight parameters were evaluated comprising type and concentration of carbon source, substrate concentration, substrate addition time, shaking, luminosity, temperature and extraction time. Sixteen different culture conditions were tested in this screening. After LC-MS analysis, several biotransformation products were identified and naringenin was identified as the major product. Eleven biotransformation products were detected in Ft-HRMS analyses and identified as naringenin as major compound, 4’-methoxynaringenin, 4’-methoxynaringin, rhoifolin, apigenin, methoxyapigenin, acetylated naringin, and also two biflavonoids and two triflavonoids. Ft-HRMSn showed to be a powerful technique for structural elucidation of flavonoid biotransformation products. The fungus was capable to perform deglycosylation, reduction and O-methylation reactions at this substrate indicating good enzymatic potential, since these reactions weren’t observed before for this fungus-genus.