Huang_2019_J.Agric.Food.Chem_67_8548

Reference

Title : Biodegradation of Structurally Diverse Phthalate Esters by a Newly Identified Esterase with Catalytic Activity toward Di(2-ethylhexyl) Phthalate - Huang_2019_J.Agric.Food.Chem_67_8548
Author(s) : Huang H , Zhang XY , Chen TL , Zhao YL , Xu DS , Bai YP
Ref : Journal of Agricultural and Food Chemistry , 67 :8548 , 2019
Abstract :

Herein, we report a double enzyme system to degrade 12 phthalate esters (PAEs), particularly bulky PAEs, such as the widely used bis(2-ethylhexyl) phthalate (DEHP), in a one-pot cascade process. A PAE-degrading bacterium, Gordonia sp. strain 5F, was isolated from soil polluted with plastic waste. From this strain, a novel esterase (GoEst15) and a mono(2-ethylhexyl) phthalate hydrolase (GoEstM1) were identified by homology-based cloning. GoEst15 showed broad substrate specificity, hydrolyzing DEHP and 10 other PAEs to monoalkyl phthalates, which were further degraded by GoEstM1 to phthalic acid. GoEst15 and GoEstM1 were heterologously coexpressed in Escherichia coli BL21 (DE3), which could then completely degrade 12 PAEs (5 mM), within 1 and 24 h for small and bulky substrates, respectively. To our knowledge, GoEst15 is the first DEHP hydrolase with a known protein sequence, which will enable protein engineering to enhance its catalytic performance in the future.

PubMedSearch : Huang_2019_J.Agric.Food.Chem_67_8548
PubMedID: 31266305
Gene_locus related to this paper: gorpv-h6n0g6

Related information

Substrate DEHP
Gene_locus gorpv-h6n0g6

Citations formats

Huang H, Zhang XY, Chen TL, Zhao YL, Xu DS, Bai YP (2019)
Biodegradation of Structurally Diverse Phthalate Esters by a Newly Identified Esterase with Catalytic Activity toward Di(2-ethylhexyl) Phthalate
Journal of Agricultural and Food Chemistry 67 :8548

Huang H, Zhang XY, Chen TL, Zhao YL, Xu DS, Bai YP (2019)
Journal of Agricultural and Food Chemistry 67 :8548