Ece Selin, Lambertz Camilla, Fischer Rainer, Commandeur Ulrich
Institute for Molecular Biotechnology (Biology VII), RWTH Aachen University, Worringerweg 1, 52074, Aachen, Germany.
Fraunhofer Institute for Molecular Biology and Applied Ecology (IME), Forckenbeckstrasse 6, 52074, Aachen, Germany.
AMB Express. 2017 Dec;7(1):86. doi: 10.1186/s13568-017-0387-0. Epub 2017 Apr 24.
Laccases are used for the conversion of biomass into fermentable sugars but it is difficult to produce high yields of active laccases in heterologous expression systems. We overcame this challenge by expressing Streptomyces cyaneus CECT 3335 laccase in Escherichia coli (ScLac) and we achieved a yield of up to 104 mg L following purification by one-step affinity chromatography. Stability and activity assays using simple lignin model substrates showed that the purified enzyme preparation was active over a broad pH range and at high temperatures, suggesting it would be suitable for biomass degradation. The reusability of ScLac was also demonstrated by immobilizing the enzyme on agarose beads with a binding yield of 33%, and by the synthesis of cross-linked enzyme aggregates with an initial activity recovery of 72%.
漆酶可用于将生物质转化为可发酵糖,但在异源表达系统中难以高产活性漆酶。我们通过在大肠杆菌中表达蓝链霉菌CECT 3335漆酶(ScLac)克服了这一挑战,经一步亲和层析纯化后,产量高达104 mg/L。使用简单木质素模型底物进行的稳定性和活性测定表明,纯化后的酶制剂在较宽的pH范围和高温下均具有活性,这表明它适用于生物质降解。通过将酶固定在琼脂糖珠上(结合率为33%)以及合成交联酶聚集体(初始活性回收率为72%),也证明了ScLac的可重复使用性。