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Effect of POX genotype and Lip2p overexpression on lactone production and reconsumption by Yarrowia lipolytica using castor oil as substrate

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Detalhes bibliográficos
Resumo:γ-Decalactone production from ricinoleic acid biotransformation by Yarrowia lipolytica has drawn the attention of many authors and, in the last years, molecular and physiological developments were made through the use of engineered strains in novel culture conditions. The purpose of this work was to monitor the performance of modified Y. lipolytica strains in their lipid metabolism specifically at the β-oxidation pathway (MTLY40-2P strain, disrupted in the native genes POX2-5 and expressing an ectopic Aox2p-encoding gene) or at the triglyceride hydrolysis (JMY3010 strain, Lip2p overexpressed) using castor oil as substrate, in a lab-scale bioreactor. Using step-wise fed-batch cultures of MTLY40-2P strain, a γ-decalactone concentration of 7 g L−1 was reached. γ-Decalactone reconsumption was prevented and hydroxylactone production was reduced by Y. lipolytica MTLY40-2P strain. Moreover, substantial increase in the initial rate of aroma production was obtained with strain overexpressing LIP2 gene due to the fast hydrolysis of castor oil.
Autores principais:Braga, Adelaide
Outros Autores:Crutz-Le Coq, A. M.; Dulermo, R.; Nicaud, J. M.; Belo, Isabel
Assunto:β-Oxidation Castor oil γ-Decalactone production Lipase Yarrowia lipolytica beta-Oxidation gamma-Decalactone production ?-Decalactone production
Ano:2015
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
Descrição
Resumo:γ-Decalactone production from ricinoleic acid biotransformation by Yarrowia lipolytica has drawn the attention of many authors and, in the last years, molecular and physiological developments were made through the use of engineered strains in novel culture conditions. The purpose of this work was to monitor the performance of modified Y. lipolytica strains in their lipid metabolism specifically at the β-oxidation pathway (MTLY40-2P strain, disrupted in the native genes POX2-5 and expressing an ectopic Aox2p-encoding gene) or at the triglyceride hydrolysis (JMY3010 strain, Lip2p overexpressed) using castor oil as substrate, in a lab-scale bioreactor. Using step-wise fed-batch cultures of MTLY40-2P strain, a γ-decalactone concentration of 7 g L−1 was reached. γ-Decalactone reconsumption was prevented and hydroxylactone production was reduced by Y. lipolytica MTLY40-2P strain. Moreover, substantial increase in the initial rate of aroma production was obtained with strain overexpressing LIP2 gene due to the fast hydrolysis of castor oil.