Engineering of a fungal laccase to develop a robust, versatile and highly-expressed biocatalyst for sustainable chemistry

被引:36
作者
de Salas, Felipe [1 ]
Aza, Pablo [1 ]
Gilabert, Joan F. [2 ]
Santiago, Gerard [2 ,3 ]
Kilic, Sibel [4 ]
Sener, Mehmet E. [4 ]
Vind, Jesper [5 ]
Guallar, Victor [2 ,6 ]
Martinez, Angel T. [1 ]
Camarero, Susana [1 ]
机构
[1] CSIC, Ctr Invest Biol, Ramiro de Maeztu 9, Madrid 28040, Spain
[2] Barcelona Supercomp Ctr, Jordi Girona 29, E-08034 Barcelona, Spain
[3] Nostrum Biodiscovery, Jordi Girona 29,Nexus 2 D128, Barcelona 08034, Spain
[4] Setas Kimya San AS, Karanfil Sok 34, TR-34330 Istanbul, Turkey
[5] Novozymes A S, Krogshoejvej 36, DK-2880 Bagsvaerd, Denmark
[6] ICREA, Passeig Lluis Co 23, E-08010 Barcelona, Spain
基金
欧盟地平线“2020”;
关键词
DIRECTED EVOLUTION; MELANOCARPUS-ALBOMYCES; CATALYTIC-PROPERTIES; MOLECULAR-CLONING; CRYSTAL-STRUCTURE; C-TERMINUS; STABILITY; MUTAGENESIS;
D O I
10.1039/c9gc02475a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fungal laccases can play an important role as biocatalysts in organic chemistry to replace chemical synthesis. In a previous work we synthesized conductive polyaniline using a high-redox potential laccase from our collection of recombinant fungal variants. Still, the oxidation of aniline is hindered by the reaction conditions (low pH and presence of anionic surfactants). Thus, we tackle here the directed evolution of the enzyme assisted by computational simulation aiming at improving aniline oxidation at the required polymerization conditions while maintaining the enzyme's substrate promiscuity. Simultaneously, its secretion by the host used for the engineering (Saccharomyces cerevisiae) was enhanced. Then, the improved laccase variant was overproduced in the industrial host Aspergillus oryzae and assayed for one-pot synthesis of polyaniline and naphtol-derived dyes whose textile dyeing properties were verified in an industrial environment. Finally, modification of its C-terminal tail further enhanced laccase stability by flexibilization of the region. The resulting biocatalyst displays noticeable stability at high temperature and extreme pH while shows improved k(cat) values on the different substrates tested. Moreover, it is remarkably produced in S. cerevisiae at rates not formerly reported in the literature. These facts, together with the overexpression in A. oryzae opens new scenarios for its further development and application.
引用
收藏
页码:5374 / 5385
页数:12
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