Department of Biology, Washington University in St. Louis, St. Louis, MO 63130.
Department of Chemical Engineering, Pennsylvania State University, University Park, PA 16802.
Proc Natl Acad Sci U S A. 2018 Dec 11;115(50):E11761-E11770. doi: 10.1073/pnas.1814912115. Epub 2018 Nov 8.
Cyanobacteria are emerging as attractive organisms for sustainable bioproduction. We previously described UTEX 2973 as the fastest growing cyanobacterium known. 2973 exhibits high light tolerance and an increased photosynthetic rate and produces biomass at three times the rate of its close relative, the model strain 7942. The two strains differ at 55 genetic loci, and ome of these loci must contain the genetic determinants of rapid photoautotrophic growth and improved photosynthetic rate. Using CRISPR/Cpf1, we performed a comprehensive mutational analysis of 2973 and identified three specific genes, , , and , with SNPs that confer rapid growth. The fast-growth-associated allele of each gene was then used to replace the wild-type alleles in 7942. Upon incorporation, each allele successively increased the growth rate of 7942; remarkably, inclusion of all three alleles drastically reduced the doubling time from 6.8 to 2.3 hours. Further analysis revealed that our engineering effort doubled the photosynthetic productivity of 7942. We also determined that the fast-growth-associated allele of yielded an ATP synthase with higher specific activity, while that of encoded a NAD kinase with significantly improved kinetics. The SNPs cause broad changes in the transcriptional profile, as this gene is the master output regulator of the circadian clock. This pioneering study has revealed the molecular basis for rapid growth, demonstrating that limited genetic changes can dramatically improve the growth rate of a microbe by as much as threefold.
蓝藻作为可持续生物生产的有吸引力的生物而崭露头角。我们之前曾描述过 UTEX 2973 是已知生长最快的蓝藻。2973 表现出对高光的耐受性,光合速率提高,其生物量的产生速度是近亲模式菌株 7942 的三倍。这两个菌株在 55 个遗传基因座上存在差异,其中一些基因座一定包含快速光自养生长和提高光合速率的遗传决定因素。我们使用 CRISPR/Cpf1 对 2973 进行了全面的突变分析,鉴定出三个具有 SNP 的特定基因 、 、 和 ,这些 SNP 赋予了快速生长的能力。然后,每个基因的快速生长相关等位基因被用来替换 7942 中的野生型等位基因。在整合后,每个等位基因都相继提高了 7942 的生长速度;值得注意的是,包含所有三个等位基因使倍增时间从 6.8 小时急剧缩短到 2.3 小时。进一步的分析表明,我们的工程努力使 7942 的光合生产力提高了一倍。我们还确定, 快速生长相关等位基因的 ATP 合酶具有更高的比活性,而 编码的 NAD 激酶具有显著改善的动力学特性。 基因的快速生长相关等位基因导致转录谱发生广泛变化,因为该基因是生物钟的主输出调节剂。这项开创性的研究揭示了快速生长的分子基础,表明有限的遗传变化可以使微生物的生长速度提高三倍。