Induction of Gene Expression Using a High Concentration Sugar Mixture

a high-concentration sugar and gene expression technology, applied in the field of protein production improvement methods, can solve the problems of high cost associated with cellulase production, the problem of controlling the glucose concentration of i>trichoderma /i>grown on solid cellulose, and the problem of high cost of cellulase production

Inactive Publication Date: 2010-01-14
ENGLAND GEORGE R +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0015]It has now been discovered that when a whole cellulase preparation is added to a concentrated glucose solution, and the composition is incubated for at least two days at 50° C. to about 65° C., a sugar mixture containing appreciable quantities of an inducer of cellulase gene expression is produced. Surprisingly, the resulting complex mixture is sufficient to induce cellulase production as is without further purification. This discovery is surprising since glucose acts as a repressor of cellulase genes in Trichoderma reesei. This discovery provides an inducer of cellulase gene expression that is an inexpensive alternative to lactose or purified sophorose and a less cumbersome alternative to solid cellulose for the production of cellulases in Trichoderma reesei.

Problems solved by technology

The most problematic and expensive aspect of industrial cellulase production is providing the appropriate inducer to Trichoderma.
Unfortunately on an industrial scale, both methods of induction have drawbacks which result in high costs being associated with cellulase production.
Although cellulose is an effective and inexpensive inducer, controlling the glucose concentration when Trichoderma is grown on solid cellulose can be problematic.
At low concentrations of cellulose, glucose production may be too slow to meet the metabolic needs of active cell growth and function.
Thus, expensive process control schemes are required to provide slow substrate addition and monitoring of glucose concentration (Ju and Afolabi, Biotechnol. Prog., 91-97, 1999).
Moreover, the slow continuous delivery of substrate can be difficult to achieve as a result of the solid nature of the cellulosic materials.
Purification of the β-glucosidase is both time-consuming and expensive.
Sophorose is a more potent inducer than cellulose, but sophorose is expensive and difficult to manufacture.
Thus, while it is easier to handle and control than solid cellulose, sophorose can nonetheless make the cost of producing cellulases prohibitively expensive and, thus, is impractical for commercial cellulase production.

Method used

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  • Induction of Gene Expression Using a High Concentration Sugar Mixture
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  • Induction of Gene Expression Using a High Concentration Sugar Mixture

Examples

Experimental program
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Effect test

example 1

[0123]This example illustrates how an inducing feed composition for stimulating the expression of cellulase genes in Trichoderma reesei was prepared. The incubation was run at the pH of the solution, i.e., 5.0. For beta-glucosidase the incubation was found to be best at pH 4.0-6.5.

[0124](i) A 60% (w / w) glucose solution was sterilized for 30 minutes at 121° C., 2.2 bar pressure.

[0125](ii) Sterile whole cellulase preparation was added to the glucose solution to a final concentration of 1 0 g total protein / L.

[0126](iii) The tank containing the glucose and whole cellulase mixture was held at 65° C. for 3 days with 75 RPM mixing.

[0127](iv) Following incubation, the sterile solution was harvested to an appropriate container for fermentation feeding.

[0128]The resulting inducing feed composition was found to have 16.1 g / L Sophorose, 47.5 g / L Gentiobiose, and approximately 600 g / L Glucose. Other sugars may be present but were not analyzed.

[0129]Inducing feed solutions have also been prepared...

example 2

[0132]The following example details how a glucose / sophorose feed is made and used to produce cellulase enzyme during fermentation.

I. Production of Glucose / Sophorose Feed:

[0133]60% (w / w) glucose solution was dissolved and sterilized for 30 minutes at 121° C. The temperature was decreased to 65° C. and 10 g of total protein (whole cellulase previously produced by T. reesei) / L was added. The mixture was agitated slowly and held at 65° C. for 3 days. The sophorose content was measured at 12 g / L in this 60% glucose solution.

II. Fermentation

[0134]0.8 L of media was inoculated with 1.5 ml Trichoderma reesei RL-P37 frozen spore suspension as a seed flask. This flask was split into two 0.4 L portions and transferred to 2×7 L of fermentation media in two different 15 L Biolafitte fermentors after 48 hours. The growth media had the following composition:

Media componentg / LKH2PO44(NH4)2SO46.35MgSO4—7H2O2CaCl2—2H2O0.53Glucose50Corn Steep Solids6.25(Roquette)Trace elements*1ml / LTrace elements*: 5 ...

example 3

[0137]The following example details how a glucose / sophorose feed is made and used to produce a heterologous protein from a filamentous fungus during fermentation.

[0138]The inducing feed composition is prepared using the procedure in Example 1.

[0139]An expression plasmid for use in transforming Trichoderma reesei is constructed as follows. The ends of the gene encoding protein of interest are blunted by T4 DNA polymerase and inserted into Pmel restriction site of the Trichoderma expression vector, pTEX, see PCT Publication No. WO 96 / 23928, which publication is herein incorporated by reference, which contains a CBH1 promoter and terminator for gene expression and a Trichoderma pyr4 gene as a selection marker for transformants. The linear DNA fragment containing only the CBH1 promoter, the gene encoding the protein of interest, the CBH1 terminator and selection marker pyr4 is isolated from a gel and used to transform a uridine auxotroph strain of Trichoderma reesei (see U.S. Pat. No. 5...

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Abstract

Described herein is a composition useful for inducing expression of genes whose expression is under control of an inducible promoter sequence and methods for the compositions preparation and use.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims priority to U.S. Provisional Application No. 60 / 409,466, filed Sep. 10, 2002 (Attorney Docket No. GC774P), which is herein incorporated in its entirety by reference.STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT[0002]Portions of this work were funded by Subcontract No. ZCO-0-30017-01 with the National Renewable Energy Laboratory under Prime Contract No. DE-AC36-99GO10337 with the U.S. Department of Energy. Accordingly, the United States Government may have certain rights in this invention.FIELD OF THE INVENTION[0003]This invention relates to methods for improved production of proteins from a cell culture. The inventors have discovered culture components and conditions that dramatically increase the amount of protein produced from genes under the control of cellulase gene promoter sequences. The improved methods can be used for the production of proteins encoded by natur...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12P21/00C12N9/42A61P21/02A61P41/00C12N1/14C12N1/38C12P1/00C12P19/12C12P19/14C12P21/02
CPCC12N1/14C12N1/38C12P19/12C12N9/2445C12P21/02C12Y302/01021C12N9/2437C12P19/14A61P21/02A61P41/00
Inventor ENGLAND, GEORGE R.KELLEY, AARONMITCHINSON, COLIN
Owner ENGLAND GEORGE R
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