Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Cellulosome enzymic preparation for catalyzing saccharification of lignocellulose

A technology of lignocellulose and cellulosomes, which is applied in the field of enzyme preparations and cellulosome enzyme preparations, can solve problems such as high cost and cumbersome process, and achieve the effects of improving synergy, reducing consumption, and achieving stability and activity

Active Publication Date: 2018-12-11
QINGDAO INST OF BIOENERGY & BIOPROCESS TECH CHINESE ACADEMY OF SCI
View PDF6 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The cellulosome enzyme preparation solves the problems of high cost and cumbersome process caused by the consumption of enzymes in the saccharification process

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Cellulosome enzymic preparation for catalyzing saccharification of lignocellulose
  • Cellulosome enzymic preparation for catalyzing saccharification of lignocellulose
  • Cellulosome enzymic preparation for catalyzing saccharification of lignocellulose

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Example 1: Construction of Clostridium thermocellum expressing exocrine β-1,4 glucosidase

[0040] The cellulase Cel9K (exocellulase, encoded by the nucleic acid sequence 2113813 to 2111293 in the genome CP002416.1) in the cellulosome of Clostridium thermocellum and the docking module were selected as the targeted knock-in site point. First, the gene encoding β-1,4-glucosidase BglA (GENBANK sequence number is AFO70070.1) was used as the target sequence, and cloned into the homologous recombination plasmid pHK-HR( figure 2 ), construct the homologous recombination plasmid pHK-HR-BglA. The upstream homology arm HR-up sequence is the nucleic acid sequence from 2111347 to 2112870 in the Clostridium thermocellum DSM1313 genome (the sequence number in the NCBI database is CP002416.1), and the downstream homology arm HR-down is the 2109848 to 2111354 nucleic acid sequence in the DSM1313 genome, The middle homology arm HR-short is the nucleic acid sequence from 2111347 to 21...

Embodiment 2

[0045] Embodiment 2: By the method of direct connection, construct the cellulosomal enzyme preparation based on Clostridium thermocellum cellulite

[0046] Using the method of overlap extension polymerase chain reaction, the sequence (SEQ ID NO: 10) of the type II adhesion module CohIIct of xylanase XynC (SEQ ID NO: 1) and Clostridium thermocellum or the type I docking module DocIct The sequence (SEQ ID NO: 9) is directly connected, wherein the sequence of CohIIct or DocIct is connected to the 3' end of the XynC sequence, thereby obtaining the XynC-CohIIct and XynC-DocIct sequences. Using BamHI and XbaI restriction sites again, the recombinant sequence connected together was cloned into the expression plasmid pHK( figure 1 )superior. Since pHK carries the promoter and signal peptide sequence (SEQ ID NO: 11) of the cellulase Cel48S derived from Clostridium thermocellum, the expressed target gene can be secreted to the extracellular space. The constructed plasmid was transform...

Embodiment 3

[0047] Embodiment 3: By the method of direct connection, construct the cellulosomal enzyme preparation based on Clostridium thermocellum cellulosome

[0048] The gene encoding xylanase XynB (SEQ ID NO: 2) was used as the target sequence, and 5 of the cellulosic exonuclease Cel48S (encoded by the nucleic acid sequence from 3228088 to 3230229 in genome CP002416.1) of Clostridium thermocellum was selected. The 'end was used as the targeted knock-in site, and cloned into the homologous recombination plasmid pHK-HR( figure 2 ), construct the homologous recombination plasmid pHK-HR-xynB. The upstream homology arm HR-up is the nucleotide sequence from 3230200 to 3230700 in the genome of Clostridium thermocellum DSM1313 (the sequence number in the NCBI database is CP002416.1), the downstream homology arm HR-down is the nucleotide sequence from 3229699 to 3230199 in the DSM1313 genome, and the middle The homology arm HR-short is the nucleic acid sequence from 3230200 to 3230500 in th...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a cellulosome enzymic preparation for catalyzing saccharification of lignocellulose aiming at the problem of cellulosome in lignocellulosic saccharification in the prior art. The cellulosome enzymic preparation for catalyzing the saccharification of lignocellulose is a protein complex obtained by binding non-cellulosome proteins in cellulosome through the mutual action of non-cellulosome proteins and components in the cellulosome; then the protein complex is used for saccharifying, namely, bacterial cells are not involved in the saccharification process. The cellulosomeenzymic preparation provided by the invention not only achieves the maintenance of stability and activity, but also greatly enhances the synergistic effect with other enzymes in the system, thereby reducing the enzyme consumption, and reducing the production cost and the trivialness of the process.

Description

technical field [0001] The invention belongs to the field of biotechnology and relates to an enzyme preparation, in particular to a cellulosome enzyme preparation for catalyzing lignocellulose saccharification. Background technique [0002] Lignocellulose is a kind of renewable material with abundant supply and environmental friendliness. It is the only resource that can be regenerated on a large scale and completely replace fossil energy. Vigorously developing the utilization of lignocellulose raw materials in energy and other fields is the key to speeding up the development of circular economy and ensuring An important strategic task for national energy security and carbon emission reduction. However, the biggest bottleneck of lignocellulose conversion is the refractory degradation of the cellulose crystallization region, resulting in low enzymatic hydrolysis efficiency and high cost. Therefore, to achieve efficient utilization of lignocellulose, it is necessary to first ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07K19/00C12N9/24C12N9/26C12N9/50C12P19/14C12P19/00
CPCC07K14/00C07K2319/00C12N9/2411C12N9/248C12N9/50C12P19/00C12P19/14C12Y302/01004
Inventor 崔球刘亚君李仁民刘世岳祁宽冯银刚
Owner QINGDAO INST OF BIOENERGY & BIOPROCESS TECH CHINESE ACADEMY OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com