Li Tingting, Li Chien-Ting, Butler Kirk, Hays Stephanie G, Guarnieri Michael T, Oyler George A, Betenbaugh Michael J
Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD 21218 USA.
Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218 USA.
Biotechnol Biofuels. 2017 Mar 21;10:55. doi: 10.1186/s13068-017-0736-x. eCollection 2017.
The feasibility of heterotrophic-phototrophic symbioses was tested via pairing of yeast strains , , or with a sucrose-secreting cyanobacterium .
The phototroph showed no growth in standard BG-11 medium with yeast extract, but grew well in BG-11 medium alone or supplemented with yeast nitrogen base without amino acids (YNB w/o aa). Among three yeast species, and adapted well to the BG-11 medium supplemented with YNB w/o aa, sucrose, and various concentrations of NaCl needed to maintain sucrose secretion from , while growth of was highly dependent on sucrose levels. and grew efficiently and utilized sucrose produced by the partner in co-culture. Co-cultures of and were sustained over 1 month in both batch and in semi-continuous culture, with the final biomass and overall lipid yields in the batch co-culture 40 to 60% higher compared to batch mono-cultures of The co-cultures showed enhanced levels of palmitoleic and linoleic acids. Furthermore, cyanobacterial growth in co-culture with was significantly superior to axenic growth, as was unable to grow in the absence of the yeast partner when cultivated at lower densities in liquid medium. Accumulated reactive oxygen species was observed to severely inhibit axenic growth of cyanobacteria, which was efficiently alleviated through catalase supply and even more effectively with co-cultures of .
The pairing of a cyanobacterium and eukaryotic heterotroph in the artificial lichen of this study demonstrates the importance of mutual interactions between phototrophs and heterotrophs, e.g., phototrophs provide a carbon source to heterotrophs, and heterotrophs assist phototrophic growth and survival by removing/eliminating oxidative stress. Our results establish a potential stable production platform that combines the metabolic capability of photoautotrophs to capture inorganic carbon with the channeling of the resulting organic carbon directly to a robust heterotroph partner for producing biofuel and other chemical precursors.
通过将酵母菌株、或与分泌蔗糖的蓝细菌配对,测试了异养 - 光养共生的可行性。
光养生物在含有酵母提取物的标准BG - 11培养基中未生长,但在单独的BG - 11培养基或补充了无氨基酸酵母氮源(YNB w/o aa)的BG - 11培养基中生长良好。在三种酵母物种中,和能很好地适应补充了YNB w/o aa、蔗糖以及维持分泌蔗糖所需的各种浓度NaCl的BG - 11培养基,而的生长高度依赖于蔗糖水平。和在共培养中能高效生长并利用伙伴产生的蔗糖。和的共培养在分批培养和半连续培养中均能维持1个月以上,分批共培养中的最终生物量和总脂质产量比的分批单培养高40%至60%。共培养显示棕榈油酸和亚油酸水平有所提高。此外,与共培养时蓝细菌的生长明显优于无菌生长,因为在液体培养基中以较低密度培养时,在没有酵母伙伴的情况下无法生长。观察到积累的活性氧严重抑制蓝细菌的无菌生长,通过供应过氧化氢酶可有效缓解,与共培养时效果更显著。
本研究人工地衣中蓝细菌与真核异养生物的配对证明了光养生物和异养生物之间相互作用的重要性,例如,光养生物为异养生物提供碳源,而异养生物通过消除氧化应激来协助光养生物的生长和存活。我们的结果建立了一个潜在的稳定生产平台,该平台将光合自养生物捕获无机碳的代谢能力与将产生的有机碳直接输送给强大的异养生物伙伴以生产生物燃料和其他化学前体的能力相结合。