%0 Journal Article
%T Expression of Pectin Lyase 1 from Aspergillus oryzae in Escherichia coli
米曲霉果胶酸酯裂解酶(pectin lyase 1)在原核系统中重组表达
%A ZHAO Qing-Xin
%A YUAN Sheng
%A ZHANG Yu-Ling
%A
赵庆新
%A 袁生
%A 张宇玲
%J 生物工程学报
%D 2007
%I
%X Pectin lyases from Aspergillus oryzae and Aspergillus niger are usually used for the production of traditional fermented foods, but these fungi produce less pectinases under natural conditions. The cDNA coding mature Pell (without signal peptide) was amplified from Aspergillus oryzae by RT-PCR. Pell cDNA was cloned into pET-28a ( + ) expression vector, then was transformed into E. coli Turner (DE3) plac I cells to express Pell with 6-His tag. For improving the efficiency of Pell expression in E. coli, the conditions of expressing the Pell in E. coli were optimized. E. coli Turner (DE3) plac I cells with pET-28a ( + )-pell was first cultivated at 37 degrees C, 220 r/min until OD600 reached about 0.8. Then, cultivation broth was added with 0.05-0.1 mmol/L IPTG and continuously incubated at 15 degrees C, at 170 r/min for 60 h for expressing of Pell. The recombinant expressed Pell activity could reach 400 u/mL medium, which is 4000-fold of Pell produced naturally by A. oryzae and superior than known recombinant amount of pectin lyases expressed in different fungi expression systems.
%K Aspergillus oryzae
%K pectin nlyase 1
%K Escherichia coli
%K expression
米曲霉
%K 果胶酸酯裂解酶1
%K 大肠杆菌
%K 表达
%U http://www.alljournals.cn/get_abstract_url.aspx?pcid=90BA3D13E7F3BC869AC96FB3DA594E3FE34FBF7B8BC0E591&jid=A66E90C274451689E69F6F0291467824&aid=6BD4FCC79FC09A87&yid=A732AF04DDA03BB3&vid=EA389574707BDED3&iid=94C357A881DFC066&sid=BF1420E7E18952EE&eid=A766A50385B9FB1F&journal_id=1000-3061&journal_name=生物工程学报&referenced_num=0&reference_num=19