Direct enzymatic esterification of cotton and Avicel with wild-type and enginee...

• Autor(es): Matamá, Maria Teresa ; Casal, Margarida ; Paulo, Artur Cavaco
• Data: 2013
• Identificador Persistente: http://hdl.handle.net/1822/22663
• Origem: RepositóriUM - Universidade do Minho
• Assunto(s): Cellulose ester; Reverse esterase; Transesterification; Carbohydrate-binding module; Caprylic acid
• Tipo de Documento: Artigo
• Idioma: Inglês

Descrição

In this work, the surface of cellulose, either Avicel or cotton fabric, was modified using cutinases without any previous treatment to swell or to solubilise the polymer. Aiming further improvement of cutinase ester synthase activity on cellulose, an engineered cutinase was investigated. Wild-type cutinase from Fusarium solani and its fusion with the carbohydrate-binding module N1 from Cellulomonas fimi were able to esterify the hydroxyl groups of cellulose with distinct efficiencies depending on the acid substrate/solvent system used, as shown by titration and by ATR-FTIR. The carbonyl stretching peak area increased significantly after enzymatic treatment during 72 h at 30 °C. Cutinase treatment resulted in relative increases of 31 and 9 % when octanoic acid and vegetable oil were used as substrates, respectively. Cutinase-N1 treatment resulted in relative increases of 11 and 29 % in the peak area when octanoic acid and vegetable oil were used as substrates, respectively. The production and application of cutinase fused with the domain N1 as a cellulose ester synthase, here reported for the first time, is therefore an interesting strategy to pursuit.