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利用多粘芽孢杆菌ICGEB2008从纤维素水解产物高效生产(R,R)-2,3-丁二醇

Efficient production of (R,R)-2,3-butanediol from cellulosic hydrolysate using Paenibacillus polymyxa ICGEB2008.

作者信息

Adlakha Nidhi, Yazdani Syed Shams

机构信息

Synthetic Biology and Biofuels Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), 10504, Aruna Asaf Ali Marg, New Delhi, 110067, India.

出版信息

J Ind Microbiol Biotechnol. 2015 Jan;42(1):21-8. doi: 10.1007/s10295-014-1542-0. Epub 2014 Nov 26.

Abstract

We report here the production of pure (R,R)-2,3-butanediol (2,3-BDO) isomer by the non-pathogenic Paenibacillus polymyxa ICGEB2008 using lignocellulosic hydrolysate as substrate. Experimental design based on Plackett-Burman resulted in identification of Mn and K as most crucial salt elements along with the yeast extract for 2,3-BDO production. Further experiments using Box-Behnken design indicated that both KCl and yeast extract together had major impact on 2,3-BDO production. Optimized medium resulted in 2,3-BDO production with 2.3-fold higher maximum volumetric productivity (2.01 g/L/h) and similar yield (0.33 g/g sugar) as compared to rich yeast extract-peptone-dextrose medium in the bioreactor studies. Considering that the balance substrate was channeled towards ethanol, carbon recovery was close to theoretical yield between the two solvents, i.e., 2,3-BDO and ethanol. Biomass hydrolysate and corn-steep liquor was used further to produce 2,3-BDO without impacting its yield. In addition, 2,3-BDO was also produced via simultaneous saccharification and fermentation, signifying robustness of the strain.

摘要

我们在此报告,非致病性多粘芽孢杆菌ICGEB2008利用木质纤维素水解产物作为底物生产纯(R,R)-2,3-丁二醇(2,3-BDO)异构体。基于Plackett-Burman的实验设计确定了Mn和K是与酵母提取物一起对2,3-BDO生产最为关键的盐元素。使用Box-Behnken设计的进一步实验表明,KCl和酵母提取物共同对2,3-BDO生产有重大影响。在生物反应器研究中,优化培养基产生的2,3-BDO产量与富含酵母提取物-蛋白胨-葡萄糖培养基相比,最大体积生产率提高了2.3倍(2.01 g/L/h),产率相似(0.33 g/g糖)。考虑到剩余底物转向了乙醇,两种溶剂(即2,3-BDO和乙醇)之间的碳回收率接近理论产率。生物质水解产物和玉米浆进一步用于生产2,3-BDO且不影响其产率。此外,2,3-BDO也通过同步糖化发酵生产,这表明该菌株具有稳健性。

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