Using an Inducible Promoter of the Glucoamylase Gene to Construct New Multienzyme Complexes from Penicillium verruculosum
- 作者: Sinitsyn A.P.1,2, Volkov P.V.3, Rubtsova E.A.3, Shashakov I.A.3, Rozhkova A.M.3, Sinitsyna O.A.1, Kondrat’eva E.G.3, Zorov I.N.1,3, Satrudinov A.D.3, Merzlov D.A.1, Matys V.Y.4
-
隶属关系:
- Moscow State University
- National Research Institute of Food Biotechnology, Division of the Federal Research Center for Food and Biotechnology
- Federal Research Center of Biotechnology
- Institute of Biochemistry and Physiology of Microorganisms
- 期: 卷 10, 编号 1 (2018)
- 页面: 75-82
- 栏目: Biocatalysis
- URL: https://journals.rcsi.science/2070-0504/article/view/202758
- DOI: https://doi.org/10.1134/S2070050418010105
- ID: 202758
如何引用文章
详细
New recombinant strains of Penicillium verruculosum are created using a new plasmid construct based on an inducible promoter of glucoamylase gene (gla1) that secretes heterologous xylanase E (XylE) from P. canescens. New biocatalysts are produced that contain cellulolytic enzyme preparations (EPs) enriched with XylE. The amount of XylE in the recombinant EPs varies in the optimum range of 11–24% of the total protein while generally preserving the P. verruculosum cellulose complex. The hydrolytic activity of the new EPs with respect to polymeric plant-derived substrates exceeds that of EPs produced using other expression systems and commercial preparations. The new EP glaX-17 surpasses in particular a control EP based on the recipient strain by 13% in the efficiency of hydrolyzing aspen wood and is 20% more efficient than the commercial EP Accelerase Duet. The new EP glaX-17 displays 25% greater efficiency (35–43%) during the hydrolysis of wheat bran than the commercial EP Accelease Duet. The effectiveness is demonstrated of using the new gla1 promoter for the production of EPs (biocatalysts) while preserving the balanced cellulose complex of the strain and optimum yield of heterologous XylE required for the deep hydrolysis of xylan-containing plant biomass.
作者简介
A. Sinitsyn
Moscow State University; National Research Institute of Food Biotechnology, Division of the Federal Research Center for Food and Biotechnology
编辑信件的主要联系方式.
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119991; Moscow, 111033
P. Volkov
Federal Research Center of Biotechnology
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119071
E. Rubtsova
Federal Research Center of Biotechnology
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119071
I. Shashakov
Federal Research Center of Biotechnology
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119071
A. Rozhkova
Federal Research Center of Biotechnology
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119071
O. Sinitsyna
Moscow State University
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119991
E. Kondrat’eva
Federal Research Center of Biotechnology
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119071
I. Zorov
Moscow State University; Federal Research Center of Biotechnology
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119991; Moscow, 119071
A. Satrudinov
Federal Research Center of Biotechnology
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119071
D. Merzlov
Moscow State University
Email: apsinitsyn@gmail.com
俄罗斯联邦, Moscow, 119991
V. Matys
Institute of Biochemistry and Physiology of Microorganisms
Email: apsinitsyn@gmail.com
俄罗斯联邦, Pushchino, 142290
补充文件
