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Commercial production of polysaccharide degrading enzymes in plants and methods of using same

a technology of polysaccharide degrading enzyme and plant, which is applied in the field of commercial production of heterologous proteins in plants, can solve the problems of crippling the ability of the economy to function, affecting the standard of living of the population, and consuming over 100 billion gallons of gasoline per year in the transportation sector alon

Inactive Publication Date: 2009-08-13
APPLIED BIOTECH INST
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

"The patent describes how to make plants that produce enzymes that break down polysaccharides, which can be used in the production of ethanol. The patent also describes how to make these plants produce the enzymes in a specific way, such as in the chloroplasts or in the cell wall. Overall, the patent shows how to create plants that can help improve the process of making ethanol."

Problems solved by technology

The US transportation sector alone consumes over 100 billion gallons of gasoline per year.
Most (˜60%) of the oil used in the US today is imported, creating a somewhat precarious situation in today's political climate because supply disruptions are highly likely and would cripple the ability of the economy to function.
Fossil petroleum resources, on which our standard of living currently depends, will likely be severely limited within the next 50-100 years.
Ethanol that is produced from corn starch, however, has not been cost-effective alternative to fossil fuels.
Because known technologies for ethanol production from plant biomass have been more costly than the market price for ethanol, ethanol will not become an important alternative to fossil fuels, unless the price of fossil fuels rises substantially.
However, its semi-crystalline structure is notoriously resistant to hydrolysis by both enzymatic and chemical means.
The economics of using corn stover or any other source of lignocellulosic biomass to produce ethanol is ominous at best and is the limiting step behind the attainment of such a goal.
This is due to the high operation costs of collecting and transporting the lignocellulosic raw material to destination plants, producing the polysaccharide-degrading enzymes and the high cost of pretreating the lignocellulosic raw material to facilitate its enzymatic degradation.
The scale-up of fermentation systems for the large volumes of enzyme required for biomass conversion would be difficult and extremely capital intensive.
Capital and operating costs of such a fermentative approach to producing cellulases are likely to be impractical due to the huge scale and capital investment that will be required.
However, these methods are very expensive and time intensive, particularly in the scale-up of cultures or herds large enough for industrial enzyme production, making them highly impractical.
Bacteria and fungi are relatively simple systems but require a large initial investment for capital equipment.
Molecular Breeding 6:37-46) have expressed an endoglucanase in Arabidopsis leaves and in tobacco tissue culture cells at high levels, but both systems are impractical for commercialization.
None of the expression systems to date have shown a practical application of producing cellulases.
However, the use of this plant is impractical for commercial production of enzymes.
It is a model organism, used because of its ease in transformation, but grows to a height of only three inches and could not possibly produce adequate amounts of enzyme for commercial purposes.

Method used

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  • Commercial production of polysaccharide degrading enzymes in plants and methods of using same
  • Commercial production of polysaccharide degrading enzymes in plants and methods of using same
  • Commercial production of polysaccharide degrading enzymes in plants and methods of using same

Examples

Experimental program
Comparison scheme
Effect test

example 1

Preparation of Plasmids

[0134]FIG. 1 shows the E1 vector, having the E1 cellulase sequence (FIG. 2, SEQ ID NO: 1), the seed-preferred promoter PGNpr2 (supra), the KDEL (SEQ ID NO: 12) endoplasmic reticulum retention sequence shown in FIG. 4A (SEQ ID NO: 2); the barley alpha-amylase signal sequence, (BAASS), which was optimized and is shown in FIG. 4B (SEQ ID NO: 3), and a pin II terminator, supra. The 35S promoter, supra, drives the selectable marker, the maize optimized PAT gene. The gene confers resistance to bialaphos. See, Gordon-Kamm et al, The Plant Cell 2:603 (1990); Uchimiya et al, Bio / Technology 11:835 (1993), and Anzai et al, Mol. Gen. Gen. 219:492 (1989). The E1 cellulase gene from Acidothermus cellulolyticus was received from NREL. For expression in maize, the first 40 amino acids were optimized to maize preferred codons. The BAASS and KDEL (SEQ ID NO: 12) sequences were added to the gene by PCR using the NREL clone as template. The PCR product moved to a PCR-ready clonin...

example 2

Transformation of Maize

[0138]Fresh immature zygotic embryos were harvested from Hi-II maize kernels at 1-2 mm in length. The general methods of Agrobacterium transformation were used as described by Japan Tobacco, at Ishida et al. 1996. “High efficiency transformation of maize (Zea mays L.) mediated by Agrobacterium tumefaciens” Nature Biotechnology 14:745-750 with the modifications described supra. Fresh embryos were treated with 0.5 ml log phase Agrobacterium strains EHA101. Bacteria were grown overnight in a rich medium with kanamycin and spectinomycin to an optical density of 0.5 at 600 nm, pelleted, then re-inoculated in a fresh 10 ml culture. The bacteria were allowed to grow into log phase and were harvested at no more dense than OD600=0.5. The bacterial culture is resuspended in a co-culture medium.

[0139]For stable transformations, embryos were transferred to a bialaphos selective agent on embryogenic callus medium and transferred thereafter every two weeks to allow growth o...

example 3

Enzyme Analysis

[0140]Six single seed from each plant (up to 10 plants per event) were assayed separately. Each seed was pulverized in an automatic seed pounder and extracted in a high-speed shaker in 1 ml of 50 mM sodium acetate, pH 5. Cell debris was pelleted and the supernatant recovered for analysis of 1) total soluble protein using the Bradford assay (Bradford, M. 1976. Anal. Biochem. 72:248) and 2) the concentration of the target protein using the assay described below.

[0141]The E1 enzyme concentration was determined through the following activity assay. The assay is performed in a microtiter plate format. An appropriate amount of extract from transgenic seed containing 1 ug of TSP is transferred to a well of a 96-well microtiter plate. The total sample volume is brought to 0.1 ml with the addition of extraction / reaction buffer. The reaction is started with the addition of 0.025 mL of 5 mM 4-methylumbelliferyl-m-D-cellobioside (MUC). The reaction is incubated at 50° C. for 30-4...

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Abstract

Expression of recombinant polysaccharide degrading enzymes in plants is described. In one embodiment, expression of the enzyme is preferentially directed to the seed of the plant. Expression may also be preferentially targeted to specific locations within the plant cell. Expression of cellulases in corn is shown. The result is the capacity to produce polysaccharide degrading enzymes in plants at commercially acceptable levels in a reliable manner. Methods of using same in production of ethanol is also described, including use of the plant-produced enzymes in the ethanol production process.

Description

[0001]This application is a continuation of previously filed and co-pending application U.S. Ser. No. 11 / 219,180, filed Sep. 2, 2005, which claims benefit under 35 U.S.C.§119(e) to previously filed and co-pending application U.S. Ser. No. 60 / 607,098, filed Sep. 3, 2004 and which application U.S. Ser. No. 11 / 219,180 is also a continuation-in-part of U.S. Ser. No. 10 / 310,292, filed Dec. 5, 2002, which claims benefit under 35 U.S.C.§ 119(e) to U.S. Ser. No. 60 / 340,035, filed Dec. 6, 2001, the contents of all such prior filings are incorporated herein by reference.GOVERNMENT INTEREST[0002]The work of this invention was funded in part by a grant from the USDA and the government has certain rights therein.FIELD OF THE INVENTION[0003]The present invention relates to commercial production of heterologous proteins in plants. More specifically, the invention is to novel methods of expressing a heterologous polysaccharide degrading enzyme in plants, particularly in grains, and to methods of ta...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A01H5/00
CPCC12N15/8242C12N15/8257C12N15/8246
Inventor HOOD, ELIZABETH E.HOWARD, JOHN A.
Owner APPLIED BIOTECH INST
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