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利用植物表达的纤维二糖水解酶与低剂量纤维素酶协同水解甘蔗渣。

The combination of plant-expressed cellobiohydrolase and low dosages of cellulases for the hydrolysis of sugar cane bagasse.

机构信息

Syngenta Centre for Sugarcane Biofuels Development, Queensland University of Technology, GPO Box 2432, 2 George Street, Brisbane, Queensland 4001 Australia ; Centre for Tropical Crops and Biocommodities, Queensland University of Technology, GPO Box 2432, 2 George Street, Brisbane, Queensland 4001 Australia.

Syngenta Biotechnology Inc., Research Triangle Park, 3054 East Cornwallis Road, Durham, NC 27709-2257 USA.

出版信息

Biotechnol Biofuels. 2014 Sep 9;7(1):131. doi: 10.1186/s13068-014-0131-9. eCollection 2014.

Abstract

BACKGROUND

The expression of biomass-degrading enzymes (such as cellobiohydrolases) in transgenic plants has the potential to reduce the costs of biomass saccharification by providing a source of enzymes to supplement commercial cellulase mixtures. Cellobiohydrolases are the main enzymes in commercial cellulase mixtures. In the present study, a cellobiohydrolase was expressed in transgenic corn stover leaf and assessed as an additive for two commercial cellulase mixtures for the saccharification of pretreated sugar cane bagasse obtained by different processes.

RESULTS

Recombinant cellobiohydrolase in the senescent leaves of transgenic corn was extracted using a simple buffer with no concentration step. The extract significantly enhanced the performance of Celluclast 1.5 L (a commercial cellulase mixture) by up to fourfold on sugar cane bagasse pretreated at the pilot scale using a dilute sulfuric acid steam explosion process compared to the commercial cellulase mixture on its own. Also, the extracts were able to enhance the performance of Cellic CTec2 (a commercial cellulase mixture) up to fourfold on a range of residues from sugar cane bagasse pretreated at the laboratory (using acidified ethylene carbonate/ethylene glycol, 1-butyl-3-methylimidazolium chloride, and ball-milling) and pilot (dilute sodium hydroxide and glycerol/hydrochloric acid steam explosion) scales. We have demonstrated using tap water as a solvent (under conditions that mimic an industrial process) extraction of about 90% recombinant cellobiohydrolase from senescent, transgenic corn stover leaf that had minimal tissue disruption.

CONCLUSIONS

The accumulation of recombinant cellobiohydrolase in senescent, transgenic corn stover leaf is a viable strategy to reduce the saccharification cost associated with the production of fermentable sugars from pretreated biomass. We envisage an industrial-scale process in which transgenic plants provide both fibre and biomass-degrading enzymes for pretreatment and enzymatic hydrolysis, respectively.

摘要

背景

在转基因植物中表达生物量降解酶(如纤维二糖水解酶)有可能通过提供补充商业纤维素酶混合物的酶源来降低生物质糖化成本。纤维二糖水解酶是商业纤维素酶混合物的主要酶类。本研究在转基因玉米秸秆叶片中表达了一种纤维二糖水解酶,并将其作为两种商业纤维素酶混合物的添加剂,用于糖化不同工艺预处理的甘蔗渣。

结果

利用不含浓缩步骤的简单缓冲液从转基因玉米衰老叶片中提取重组纤维二糖水解酶。与单独使用商业纤维素酶混合物相比,该提取物显著提高了 Celluclast 1.5 L(一种商业纤维素酶混合物)对用稀硫酸蒸汽爆破工艺预处理的中试规模甘蔗渣的糖化效果,提高了四倍。此外,提取物还能够将 Cellic CTec2(一种商业纤维素酶混合物)的糖化效果提高四倍,适用于实验室(使用酸化碳酸亚乙酯/乙二醇、1-丁基-3-甲基咪唑氯和球磨)和中试(稀氢氧化钠和甘油/盐酸蒸汽爆破)规模预处理的甘蔗渣的各种残余物。我们已经证明,在模拟工业过程的条件下,利用自来水作为溶剂,可以从衰老的、转基因玉米秸秆叶片中提取约 90%的重组纤维二糖水解酶,而叶片的组织破坏最小。

结论

在衰老的、转基因玉米秸秆叶片中积累重组纤维二糖水解酶是降低与预处理生物量生产可发酵糖相关的糖化成本的可行策略。我们设想了一种工业规模的工艺,其中转基因植物分别为预处理和酶解提供纤维和生物量降解酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7401/4172943/1274c2fe17ed/13068_2014_131_Fig1_HTML.jpg

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