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本文引用的文献

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Cell-free biosystems for biomanufacturing.无细胞生物系统在生物制造中的应用。
Adv Biochem Eng Biotechnol. 2013;131:89-119. doi: 10.1007/10_2012_159.
2
Cell-free metabolic engineering: production of chemicals by minimized reaction cascades.无细胞代谢工程:通过最小化反应级联生产化学品。
ChemSusChem. 2012 Nov;5(11):2165-72. doi: 10.1002/cssc.201200365. Epub 2012 Oct 19.
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Valorization of biomass: deriving more value from waste.生物质的增值利用:从废弃物中获得更多价值。
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Facilitated substrate channeling in a self-assembled trifunctional enzyme complex.自组装三功能酶复合物中的促进性底物通道化
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Engineering a large protein by combined rational and random approaches: stabilizing the Clostridium thermocellum cellobiose phosphorylase.通过理性设计与随机方法相结合构建大型蛋白质:稳定嗜热栖热放线菌纤维二糖磷酸化酶
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Constructing the electricity-carbohydrate-hydrogen cycle for a sustainability revolution.构建可持续发展革命的电力-碳水化合物-氢能循环。
Trends Biotechnol. 2012 Jun;30(6):301-6. doi: 10.1016/j.tibtech.2012.02.006. Epub 2012 Mar 21.
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Resistant starch from high-amylose maize increases insulin sensitivity in overweight and obese men.高直链玉米抗性淀粉可提高超重和肥胖男性的胰岛素敏感性。
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8
Enhanced microbial utilization of recalcitrant cellulose by an ex vivo cellulosome-microbe complex.通过体外细胞表面展示纤维素酶复合物提高难降解纤维素的微生物利用效率。
Appl Environ Microbiol. 2012 Mar;78(5):1437-44. doi: 10.1128/AEM.07138-11. Epub 2011 Dec 30.
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The challenge of enzyme cost in the production of lignocellulosic biofuels.木质纤维素生物燃料生产中酶成本的挑战。
Biotechnol Bioeng. 2012 Apr;109(4):1083-7. doi: 10.1002/bit.24370. Epub 2011 Nov 21.
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Chemoenzymatic synthesis of homogeneous ultralow molecular weight heparins.化学酶法合成均一的超低相对分子质量肝素。
Science. 2011 Oct 28;334(6055):498-501. doi: 10.1126/science.1207478.

非食用生物质的酶法转化为淀粉。

Enzymatic transformation of nonfood biomass to starch.

机构信息

Biological Systems Engineering Department, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.

出版信息

Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7182-7. doi: 10.1073/pnas.1302420110. Epub 2013 Apr 15.

DOI:10.1073/pnas.1302420110
PMID:23589840
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3645547/
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.

摘要

由于人口增长和人均食物消费,全球对食物的需求可能在未来 40 年内增加一倍。为了满足世界未来对食物和生物燃料及可再生材料的可持续性需求,必须大幅增加富含淀粉的谷物和富含纤维素的生物能源植物的产量,同时将农业的环境足迹和生物多样性保护最小化。在这里,我们展示了一种一锅法的酶促转化方法,通过由来自细菌、真菌和植物来源的内切葡聚糖酶、纤维二糖水解酶、纤维二糖磷酸化酶和α-葡聚糖磷酸化酶组成的非天然合成酶途径,将预处理生物质转化为淀粉。来自马铃薯α-葡聚糖磷酸化酶的特殊多肽帽对于将部分水解的纤维素中间产物向前推进到直链淀粉的合成是必不可少的。纤维素中多达 30%的脱水葡萄糖单元被转化为淀粉;剩余的纤维素被水解成葡萄糖,适合酵母在同一个生物反应器中用于生产乙醇。基于同时进行酶生物转化和微生物发酵的下一代生物精炼厂可以解决食物、生物燃料和环境的三重困境。