Oligomerization of 10,16-Dihydroxyhexadecanoic Acid and Methyl 10,16-Dihydroxyhexadecanoate Catalyzed by Lipases

Molecules

M. Beatriz Gómez-Patiño²  Julia Cassani¹  Mar໚ Eugenia Jaramillo-Flores²  L. Gerardo Zepeda-Vallejo²  Georgina Sandoval³  Manuel Jimenez-Estrada⁴ 

[1] Departamento de Sistemas Biológicos, Universidad Autónoma Metropolitana Unidad Xochimilco, Calz. del Hueso No.1100, Col. Villa Quietud, México, D.F., CP 04960, Mexico;Instituto Politécnico Nacional - ENCB, Carpio y Plan de Ayala S/N, Col. Casco de Santo Tomas, México, D.F., CP 11340, Mexico;CIATEJ, Av. Normalistas 800, Guadalajara, Jalisco 42270, Mexico;Departamento de Productos Naturales, Instituto de Química, UNAM. México, D.F. CP 04510, Mexico

关键词: lipases;    oligomerization;    natural monomer;    tomato cuticle;   

DOI  :  10.3390/molecules18089317

来源: mdpi

【 摘 要 】

The main monomer of tomato cuticle, 10,16-dihydroxyhexadecanoic acid (10,16-DHPA) and its methyl ester derivative (methyl-10,16-dihydroxyhexadecanote; methyl-10,16-DHHD), were used to study their oligomerization reactions catalyzed by five lipases: Candida antarctica lipase B (CAL-B), Rhizomucor miehei lipase (RM), Thermomyces lanuginosus lipase (TL), Pseudomonas cepacia lipase (PCL) and porcine pancreatic lipase (PPL). For 10,16-DHPA, optimum yields were obtained at 60 °C using toluene and 2-methyl-2-butanol (2M2B) as solvent, while for methyl-10,16-DHHD the bests yields were obtained in toluene and acetonitrile. Both reactions leaded to linear polyesters according to the NMR and FT-IR analysis, and there was no data indicating the presence of branched polymers. Using optimized conditions, poly(10,16-DHPA) and poly(methyl-10,16-DHHD) with Mw = 814 and Mn = 1,206 Da, and Mw = 982 and Mn = 860 Da, respectively, were formed according to their MALDI-TOF MS and ESI-MS data. The self-assembly of the polyesters obtained were analyzed by AFM.

【 授权许可】

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