Department of Biology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
Biotechnol Biofuels. 2013 Sep 16;6(1):134. doi: 10.1186/1754-6834-6-134.
There has been a great deal of interest in fuel productions from lignocellulosic biomass to minimize the conflict between food and fuel use. The bioconversion of xylose, which is the second most abundant sugar present after glucose in lignocellulosic biomass, is important for the development of cost effective bioprocesses to fuels. Rhodococcus opacus PD630, an oleaginous bacterium, accumulates large amounts of triacylglycerols (TAGs), which can be processed into advanced liquid fuels. However, R. opacus PD630 does not metabolize xylose.
We generated DNA libraries from a Streptomyces bacterium capable of utilizing xylose and introduced them into R. opacus PD630. Xsp8, one of the engineered strains, was capable of growing on up to 180 g L-1 of xylose. Xsp8 grown in batch-cultures derived from unbleached kraft hardwood pulp hydrolysate containing 70 g L-1 total sugars was able to completely and simultaneously utilize xylose and glucose present in the lignocellulosic feedstock, and yielded 11.0 g L-1 of TAGs as fatty acids, corresponding to 45.8% of the cell dry weight. The yield of total fatty acids per gram of sugars consumed was 0.178 g, which consisted primarily of palmitic acid and oleic acid. The engineered strain Xsp8 was introduced with two heterologous genes from Streptomyces: xylA, encoding xylose isomerase, and xylB, encoding xylulokinase. We further demonstrated that in addition to the introduction and the concomitant expression of heterologous xylA and xylB genes, there is another molecular target in the R. opacus genome which fully enables the functionality of xylA and xylB genes to generate the robust xylose-fermenting strain capable of efficiently producing TAGs at high xylose concentrations.
We successfully engineered a R. opacus strain that is capable of completely utilizing high concentrations of xylose or mixed xylose/glucose simultaneously, and substantiated its suitability for TAG production. This study demonstrates that the engineered strain possesses a key trait of converters for lipid-based fuels production from lignocellulosic biomass.
人们对利用木质纤维素生物质生产燃料产生了浓厚的兴趣,以尽量减少粮食和燃料使用之间的冲突。木糖是木质纤维素生物质中仅次于葡萄糖的第二大丰富糖,其生物转化对于开发具有成本效益的生物工艺以生产燃料非常重要。贪噬纤维菌(Rhodococcus opacus)PD630 是一种产油细菌,能够积累大量的三酰基甘油(TAGs),这些 TAGs 可以加工成先进的液体燃料。然而,贪噬纤维菌 PD630 不能代谢木糖。
我们从一种能够利用木糖的链霉菌中生成了 DNA 文库,并将其引入贪噬纤维菌 PD630 中。其中一个工程菌株 Xsp8 能够在高达 180 g/L 的木糖浓度下生长。在含有 70 g/L 总糖的未经漂白纸浆阔叶木浆水解物的分批培养物中生长的 Xsp8 能够完全且同时利用木质纤维素原料中的木糖和葡萄糖,并产生 11.0 g/L 的 TAG 作为脂肪酸,相当于细胞干重的 45.8%。每克消耗糖产生的总脂肪酸产量为 0.178 g,主要由棕榈酸和油酸组成。该工程菌株 Xsp8 引入了来自链霉菌的两个异源基因:xylA,编码木糖异构酶,和 xylB,编码木酮糖激酶。我们进一步证明,除了异源 xylA 和 xylB 基因的引入和伴随表达外,贪噬纤维菌基因组中还有另一个分子靶标,该靶标完全使 xylA 和 xylB 基因具有功能性,从而产生能够在高木糖浓度下高效生产 TAG 的强大木糖发酵菌株。
我们成功地构建了一株能够完全利用高浓度木糖或混合木糖/葡萄糖的贪噬纤维菌菌株,并证实了其用于 TAG 生产的适宜性。这项研究表明,该工程菌株具有从木质纤维素生物质生产基于脂质的燃料的转化关键特性。