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.2013 Apr 30;110(18):7182-7.
doi: 10.1073/pnas.1302420110. Epub 2013 Apr 15.

Enzymatic transformation of nonfood biomass to starch

Affiliations

Enzymatic transformation of nonfood biomass to starch

Chun You et al. Proc Natl Acad Sci U S A..

Abstract

The global demand for food could double in another 40 y owing to growth in the population and food consumption per capita. To meet the world's future food and sustainability needs for biofuels and renewable materials, the production of starch-rich cereals and cellulose-rich bioenergy plants must grow substantially while minimizing agriculture's environmental footprint and conserving biodiversity. Here we demonstrate one-pot enzymatic conversion of pretreated biomass to starch through a nonnatural synthetic enzymatic pathway composed of endoglucanase, cellobiohydrolyase, cellobiose phosphorylase, and alpha-glucan phosphorylase originating from bacterial, fungal, and plant sources. A special polypeptide cap in potato alpha-glucan phosphorylase was essential to push a partially hydrolyzed intermediate of cellulose forward to the synthesis of amylose. Up to 30% of the anhydroglucose units in cellulose were converted to starch; the remaining cellulose was hydrolyzed to glucose suitable for ethanol production by yeast in the same bioreactor. Next-generation biorefineries based on simultaneous enzymatic biotransformation and microbial fermentation could address the food, biofuels, and environment trilemma.

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Conflict of interest statement

Conflict of interest statement: The authors have filed a provisional patent disclosure (Zhang Y-HP, Chen H. Conversion of cellulose to starch through an in vitro synthetic enzymatic pathway. Filed on December 17, 2012.).

Figures

Fig. 1.
Fig. 1.
The enzymatic cellulose hydrolysis using endoglucanases (EGs), cellobiohydrolases (CBHs) and beta-glucosidase (BG) in cellulosic ethanol biorefinery versus the synthetic cellulose-to-amylose pathway supplemented with cellobiose phosphorylase (CBP) and potato alpha-glucan phosphorylase (PGP) (A). Characterization of synthetic starch by iodine dyeing (B), CP/MAS13C-NMR (C), and FTIR (D). Tube 1, cellulose-suspended solution; tube 2, cellulose solution plus iodine/potassium iodide; tube 3, water-soluble synthetic starch solution made from cellulose mediated by the four- enzyme mixture; tube 4, synthetic starch solution plus iodine/potassium iodide; tube 5: precipitated starch by ethanol addition; and tube 6, precipitated starch when the mixture was supplemented with glucose oxidase.
Fig. 2.
Fig. 2.
A phylogenetic tree for the selected alpha-glucan phosphorylases.
Fig. 3.
Fig. 3.
Homology structure comparison between PGP (cyan) andThermotoga maritima alpha-glucan phosphorylase (purple) (A) and photos of starch-synthesizing ability (B) from cellobiose mediated by CBP and wild-type PGP (tube 1), partially decapped PGP (tube 2), or completely decapped PGP (tube 3).
Fig. 4.
Fig. 4.
Transmission electron microscopic image of Avicel-containing nanomagnetic particles (A-NMPs) (A), photos of A-NMPs that bind with a CBM3-tagged green fluorescent protein under magnet (B), the scheme of coimmobilized PGP and CBP on the A-NMPs (C), and starch synthesis rate comparison based on glucose formation between the coimmobilized PGP–CBP and the noncomplexed PGP and CBP mixture (D).
See this image and copyright information in PMC

References

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    1. The World Economic Forum Water Initiative . Water Security: The Water-Food-Energy-Climate Nexus. Washington, DC: Island Press; 2011.
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