School of Chemical Engineering & Technology, Tianjin University, Tianjin 300072, P,R, China.
Biotechnol Biofuels. 2012 Sep 7;5(1):68. doi: 10.1186/1754-6834-5-68.
Recent studies have demonstrated that photosynthetic cyanobacteria could be an excellent cell factory to produce renewable biofuels and chemicals due to their capability to utilize solar energy and CO2 as the sole energy and carbon sources. Biosynthesis of carbon-neutral biofuel alkanes with good chemical and physical properties has been proposed. However, to make the process economically feasible, one major hurdle to improve the low cell tolerance to alkanes needed to be overcome.
Towards the goal to develop robust and high-alkane-tolerant hosts, in this study, the responses of model cyanobacterial Synechocystis PCC 6803 to hexane, a representative of alkane, were investigated using a quantitative proteomics approach with iTRAQ - LC-MS/MS technologies. In total, 1,492 unique proteins were identified, representing about 42% of all predicted protein in the Synechocystis genome. Among all proteins identified, a total of 164 and 77 proteins were found up- and down-regulated, respectively. Functional annotation and KEGG pathway enrichment analyses showed that common stress responses were induced by hexane in Synechocystis. Notably, a large number of transporters and membrane-bound proteins, proteins against oxidative stress and proteins related to sulfur relay system and photosynthesis were induced, suggesting that they are possibly the major protection mechanisms against hexane toxicity.
The study provided the first comprehensive view of the complicated molecular mechanism employed by cyanobacterial model species, Synechocystis to defend against hexane stress. The study also provided a list of potential targets to engineer Synechocystis against hexane stress.
由于能够利用太阳能和 CO2 作为唯一的能源和碳源,光合蓝藻最近的研究表明,它们可能是生产可再生生物燃料和化学品的优秀细胞工厂。已经提出了用具有良好化学和物理性质的碳中性生物燃料烷烃进行生物合成。然而,为了使该过程在经济上可行,需要克服提高细胞对烷烃低耐受性这一主要障碍。
为了开发稳健且高耐烷烃的宿主,在这项研究中,使用 iTRAQ-LC-MS/MS 技术的定量蛋白质组学方法研究了模型蓝藻集胞藻 PCC 6803 对正己烷(烷烃的代表)的反应。总共鉴定出 1492 个独特的蛋白质,约占集胞藻基因组中所有预测蛋白质的 42%。在鉴定的所有蛋白质中,分别有 164 个和 77 个蛋白质上调和下调。功能注释和 KEGG 途径富集分析表明,集胞藻中共同的应激反应被正己烷诱导。值得注意的是,大量的转运蛋白和膜结合蛋白、抗氧化应激蛋白以及与硫接力系统和光合作用相关的蛋白被诱导,表明它们可能是对抗己烷毒性的主要保护机制。
该研究提供了对模式蓝藻物种集胞藻抵御己烷胁迫的复杂分子机制的首次全面了解。该研究还提供了一组潜在的目标,用于工程化集胞藻以抵御己烷胁迫。