Department of Ecology, Environment and Plant Sciences, Stockholm Universitygrid.10548.38, Stockholm, Sweden.
Instituto de Bioquímica Vegetal y Fotosíntesis, CSIC and Universidad de Sevilla, Seville, Spain.
mBio. 2021 Aug 31;12(4):e0131421. doi: 10.1128/mBio.01314-21. Epub 2021 Aug 17.
Under diazotrophic conditions, the model filamentous, heterocyst-forming cyanobacterium sp. strain PCC 7120 develops a metabolic strategy based on the physical separation of the processes of oxygenic photosynthesis, in vegetative cells, and N fixation, in heterocysts. This strategy requires the exchange of carbon and nitrogen metabolites and their distribution along the filaments, which takes place through molecular diffusion via septal junctions involving FraCD proteins. Here, was incubated in a time course (up to 20 h) with [C]bicarbonate and N and analyzed by secondary ion mass spectrometry imaging (SIMS) (large-geometry SIMS [LG-SIMS] and NanoSIMS) to quantify C and N assimilation and distribution in the filaments. The C/C and N/N ratios measured in wild-type filaments showed a general increase with time. The enrichment was relatively homogeneous in vegetative cells along individual filaments, while it was reduced in heterocysts. Heterocysts, however, accumulated recently fixed N at their poles, in which the cyanophycin plug [multi-l-arginyl-poly(l-aspartic acid)] is located. In contrast to the rather homogeneous label found along stretches of vegetative cells, C/C and N/N ratios were significantly different between filaments both at the same and different time points, showing high variability in metabolic states. A mutant did not fix N, and the C/C ratio was homogeneous along the filament, including the heterocyst in contrast to the wild type. Our results show the consumption of reduced C in the heterocysts associated with the fixation and export of fixed N and present an unpredicted heterogeneity of cellular metabolic activity in different filaments of an culture under controlled conditions. Filamentous, heterocyst-forming cyanobacteria represent a paradigm of multicellularity in the prokaryotic world. Physiological studies at the cellular level in model organisms are crucial to understand metabolic activities and qualify specific aspects related to multicellularity. Here, we used stable isotopes (C and N) coupled to LG-SIMS and NanoSIMS imaging to follow single-cell C and N fixation and metabolic dynamics along the filaments in the model heterocyst-forming cyanobacterium sp. strain PCC 7120. Our results show a close relationship between C and N fixation and distribution in the filaments and indicate that wild-type filaments in a culture can exhibit a substantial variability of metabolic states. This illustrates how some novel properties can be appreciated by studying microbial cultures at the single-cell level.
在固氮条件下,模式丝状异形胞形成蓝藻 sp. 菌株 PCC 7120 发展出一种代谢策略,基于光合作用和固氮过程在营养细胞和异形胞中的物理分离。这种策略需要交换碳和氮代谢物,并通过涉及 FraCD 蛋白的隔膜连接进行分布,这是通过分子扩散来实现的。在这里,用 [C] 碳酸氢盐和 N 培养 ,并通过二次离子质谱成像(SIMS)(大几何 SIMS [LG-SIMS] 和 NanoSIMS)进行分析,以定量分析丝状体内 C 和 N 的同化和分布。在野生型丝状体内测量的 C/C 和 N/N 比值随时间呈普遍增加。在单个丝状体内的营养细胞中,富集相对均匀,而在异形胞中则减少。然而,异形胞在其极积累最近固定的 N,其中位于蓝藻精蛋白塞[多 l-精氨酰-聚(l-天冬氨酸)]。与在营养细胞的延伸段中发现的相当均匀的标记相反,C/C 和 N/N 比值在同一和不同时间点的丝状体内差异显著,表现出代谢状态的高度可变性。一个 突变体不能固定 N,C/C 比值在丝状体内均匀,包括异形胞,与野生型相比。我们的结果表明,在与固定 N 的固定和输出相关的异形胞中消耗了还原 C,并在受控条件下的 培养物的不同丝状体内呈现出细胞代谢活动的出乎意料的异质性。丝状异形胞形成蓝藻代表原核世界多细胞性的范例。在模式生物中进行细胞水平的生理研究对于理解代谢活动和确定与多细胞性相关的特定方面至关重要。在这里,我们使用稳定同位素(C 和 N)与 LG-SIMS 和 NanoSIMS 成像相结合,跟踪模型异形胞形成蓝藻 sp. 菌株 PCC 7120 中丝状体内单个细胞的 C 和 N 固定和代谢动态。我们的结果表明,在丝状体内 C 和 N 的固定和分布之间存在密切关系,并表明培养物中的野生型丝状体内可以表现出代谢状态的很大可变性。这说明了通过在单细胞水平研究微生物培养物如何可以欣赏到一些新的特性。