Linking Cell Size, Vmax and Km in Phototrophs and Chemotrophs: Insights From Bayesian Inference

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Risa Sasaki, Mayumi Seto
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引用次数: 0

Abstract

Microbial growth is often described in terms of resource uptake rates, making the understanding and parameterisation of these rate-limiting processes critical for microbial modelling. In phototrophic plankton, theoretical studies suggest that nutrient uptake is limited by mechanistic processes involving membrane transporters, and it has been observed that the cell-specific maximum resource uptake rate (Vmax) follows a power-law relationship with cell size, as well as a trade-off between Vmax and the half-saturation constant (Km). These constraints may also apply to chemotrophic microorganisms; however, many datasets lack direct cell-size measurements. We therefore leveraged the assumption that prokaryotic cell sizes, Vmax, and Km each follow log-normal distributions, drawing parallels with established phytoplankton scaling laws. Our analysis suggests that chemotrophic organisms generally exhibit higher maximum uptake rate per dry weight (VmaxDW) and Km values than phototrophs, and that VmaxDW and Km are not strongly correlated when all chemotroph data are combined. Furthermore, the Bayesian-derived exponents for VmaxDW and Km exceeded those expected from allometric scaling relationships based on the membrane-transport capacity observed for phototrophs, implying that a range of additional factors likely affect observed kinetic parameters.

光养生物和化养生物细胞大小、Vmax和Km的联系:来自贝叶斯推理的见解
微生物生长通常用资源吸收率来描述,这使得对这些速率限制过程的理解和参数化对微生物建模至关重要。在光营养浮游生物中,理论研究表明,营养摄取受到涉及膜转运体的机制过程的限制,并且已经观察到细胞特异性最大资源摄取速率(Vmax)与细胞大小遵循幂律关系,以及Vmax与半饱和常数(Km)之间的权衡。这些限制也可能适用于化养微生物;然而,许多数据集缺乏直接的细胞大小测量。因此,我们利用了原核细胞大小、Vmax和Km都遵循对数正态分布的假设,与已建立的浮游植物缩放规律相似。我们的分析表明,趋化营养生物的最大每干重吸收率(VmaxDW)和Km值通常高于光养生物,并且当所有趋化营养生物的数据结合起来时,VmaxDW和Km并不强相关。此外,VmaxDW和Km的贝叶斯衍生指数超出了基于光养生物观察到的膜运输能力的异速缩放关系的预期,这意味着一系列其他因素可能影响观察到的动力学参数。
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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