Madsen Mary Ann, Hamilton Graham, Herzyk Pawel, Amtmann Anna
College of Medical, Veterinary and Life Sciences, Institute of Molecular, Cell and Systems Biology, University of Glasgow, Glasgow, United Kingdom.
Glasgow Polyomics, Wolfson Wohl Cancer Research Centre, University of Glasgow, Glasgow, United Kingdom.
Front Bioeng Biotechnol. 2021 Jan 19;8:619055. doi: 10.3389/fbioe.2020.619055. eCollection 2020.
Cyanobacteria are photosynthetic prokaryotes being developed as sustainable platforms that use renewable resources (light, water, and air) for diverse applications in energy, food, environment, and medicine. Despite the attractive promise that cyanobacteria offer to industrial biotechnology, slow growth rates pose a major challenge in processes which typically require large amounts of biomass and are often toxic to the cells. Two-stage cultivation strategies are an attractive solution to prevent any undesired growth inhibition by de-coupling biomass accumulation (stage I) and the industrial process (stage II). In cyanobacteria, two-stage strategies involve costly transfer methods between stages I and II, and little work has been focussed on using the distinct growth and stationary phases of batch cultures to autoregulate stage transition. In the present study, we identified and characterised a growth phase-specific promoter, which can serve as an auto-inducible switch to regulate two-stage bioprocesses in cyanobacteria. First, growth phase-specific genes were identified from a new RNAseq dataset comparing two growth phases and six nutrient conditions in sp. PCC 6803, including two new transcriptomes for low Mg and low K. A type II NADH dehydrogenase () showed robust induction when the cultures transitioned from exponential to stationary phase growth. Behaviour of a 600-bp promoter sequence (PndbA600) was then characterised in detail following the expression of PndbA600:GFP in sp. PCC 7002. Culture density and growth media analyses showed that PndbA600 activation was not dependent on increases in culture density but on N availability and on another activating factor present in the spent media of stationary phase cultures (Factor X). PndbA600 deactivation was dependent on the changes in culture density and in either N availability or Factor X. Electron transport inhibition studies revealed a photosynthesis-specific enhancement of active PndbA600 levels. Our findings are summarised in a model describing the environmental regulation of PndbA600, which can now inform the rational design of two-stage industrial processes in cyanobacteria.
蓝细菌是光合原核生物,正被开发为可持续平台,利用可再生资源(光、水和空气)在能源、食品、环境和医学等领域进行多种应用。尽管蓝细菌为工业生物技术带来了诱人的前景,但生长速度缓慢在通常需要大量生物质且往往对细胞有毒的过程中构成了重大挑战。两阶段培养策略是一种有吸引力的解决方案,通过将生物质积累(第一阶段)和工业过程(第二阶段)解耦来防止任何不期望的生长抑制。在蓝细菌中,两阶段策略涉及第一阶段和第二阶段之间成本高昂的转移方法,并且很少有工作专注于利用分批培养的不同生长和稳定期来自动调节阶段转换。在本研究中,我们鉴定并表征了一个生长阶段特异性启动子,它可以作为一种自动诱导开关来调节蓝细菌中的两阶段生物过程。首先,从一个新的RNAseq数据集鉴定出生长阶段特异性基因,该数据集比较了聚球藻属PCC 6803在两个生长阶段和六种营养条件下的情况,包括低镁和低钾的两个新转录组。当培养物从指数生长期过渡到稳定期生长时,一种II型NADH脱氢酶()表现出强烈的诱导。然后,在聚球藻属PCC 7002中表达PndbA600:GFP后,详细表征了一个600 bp启动子序列(PndbA600)的行为。培养密度和生长培养基分析表明,PndbA600的激活不依赖于培养密度的增加,而是依赖于氮的可用性以及稳定期培养物的废培养基中存在的另一种激活因子(因子X)。PndbA600的失活依赖于培养密度以及氮可用性或因子X的变化。电子传递抑制研究揭示了活性PndbA600水平的光合作用特异性增强。我们的发现总结在一个描述PndbA600环境调节的模型中,该模型现在可以为蓝细菌中两阶段工业过程的合理设计提供信息。