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在转基因水稻中高水平表达嗜热纤维梭菌β-1,4-内切葡聚糖酶可增强其秸秆在奶牛胃液中的水解。

High level expression of Acidothermus cellulolyticus β-1, 4-endoglucanase in transgenic rice enhances the hydrolysis of its straw by cultured cow gastric fluid.

机构信息

Institute of Bioagricultural Science, National Chiayi University, Chiayi, 60004 Taiwan.

出版信息

Biotechnol Biofuels. 2011 Dec 10;4:58. doi: 10.1186/1754-6834-4-58.

Abstract

BACKGROUND

Large-scale production of effective cellulose hydrolytic enzymes is the key to the bioconversion of agricultural residues to ethanol. The goal of this study was to develop a rice plant as a bioreactor for the large-scale production of cellulose hydrolytic enzymes via genetic transformation, and to simultaneously improve rice straw as an efficient biomass feedstock for conversion of cellulose to glucose.

RESULTS

In this study, the cellulose hydrolytic enzyme β-1, 4-endoglucanase (E1) gene, from the thermophilic bacterium Acidothermus cellulolyticus, was overexpressed in rice through Agrobacterium-mediated transformation. The expression of the bacterial E1 gene in rice was driven by the constitutive Mac promoter, a hybrid promoter of Ti plasmid mannopine synthetase promoter and cauliflower mosaic virus 35S promoter enhancer, with the signal peptide of tobacco pathogenesis-related protein for targeting the E1 protein to the apoplastic compartment for storage. A total of 52 transgenic rice plants from six independent lines expressing the bacterial E1 enzyme were obtained that expressed the gene at high levels without severely impairing plant growth and development. However, some transgenic plants exhibited a shorter stature and flowered earlier than the wild type plants. The E1 specific activities in the leaves of the highest expressing transgenic rice lines were about 20-fold higher than those of various transgenic plants obtained in previous studies and the protein amounts accounted for up to 6.1% of the total leaf soluble protein. A zymogram and temperature-dependent activity analyses demonstrated the thermostability of the E1 enzyme and its substrate specificity against cellulose, and a simple heat treatment can be used to purify the protein. In addition, hydrolysis of transgenic rice straw with cultured cow gastric fluid for one hour at 39°C and another hour at 81°C yielded 43% more reducing sugars than wild type rice straw.

CONCLUSION

Taken together, these data suggest that transgenic rice can effectively serve as a bioreactor for the large-scale production of active, thermostable cellulose hydrolytic enzymes. As a feedstock, direct expression of large amount of cellulases in transgenic rice may also facilitate saccharification of cellulose in rice straw and significantly reduce the costs for hydrolytic enzymes.

摘要

背景

大规模生产有效的纤维素水解酶是将农业废弃物生物转化为乙醇的关键。本研究的目的是通过遗传转化将水稻植株开发为生物反应器,大规模生产纤维素水解酶,并同时提高稻草作为高效生物质原料的性能,将纤维素转化为葡萄糖。

结果

本研究中,来源于嗜热细菌嗜酸热纤维单胞菌的纤维素水解酶β-1,4-内切葡聚糖酶(E1)基因通过根癌农杆菌介导转化在水稻中过表达。细菌 E1 基因在水稻中的表达由组成型 Mac 启动子驱动,该启动子是 Ti 质粒毛叶车前合成酶启动子和花椰菜花叶病毒 35S 启动子增强子的杂种启动子,带有烟草病程相关蛋白的信号肽,将 E1 蛋白靶向质外体空间进行储存。共获得了 6 个独立转化株系的 52 株转基因水稻植株,这些植株高水平表达该基因而不严重损害植物生长和发育。然而,一些转基因植株比野生型植株矮,开花更早。最高表达的转基因水稻株系叶片中 E1 酶的比活性比以前的研究中获得的各种转基因植物高 20 倍左右,蛋白质含量高达叶片总可溶性蛋白的 6.1%。同工酶和温度依赖性活性分析表明 E1 酶的热稳定性及其对纤维素的底物特异性,简单的热处理即可用于纯化该蛋白。此外,用培养的牛胃液在 39°C 处理转基因水稻秸秆 1 小时,然后在 81°C 处理 1 小时,产生的还原糖比野生型水稻秸秆多 43%。

结论

综上所述,这些数据表明,转基因水稻可以有效地作为大规模生产活性、耐热纤维素水解酶的生物反应器。作为一种饲料原料,大量纤维素酶在转基因水稻中的直接表达也可能促进水稻秸秆中纤维素的糖化,并显著降低水解酶的成本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c135/3307496/c759cdfe2f4b/1754-6834-4-58-1.jpg

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