Understanding systems level metabolic adaptation resulting from osmotic stress

Author:

Tremblay AlexandreORCID,Bekiaris Pavlos StephanosORCID,Klamt SteffenORCID,Mahadevan RadhakrishnanORCID

Abstract

AbstractAn organism’s survival hinges on maintaining the right thermodynamic conditions. Osmotic constraints limit the concentration range of metabolites, affecting essential cellular pathways. Despite extensive research on osmotic stress and growth, understanding remains limited, especially in hypo-osmotic environments. To delve into this, we developed a novel modeling approach that considers metabolic fluxes and metabolite concentrations along with thermodynamics. Our analysis ofE. coliadaptation reveals insights into growth rates, metabolic pathways, and thermodynamic bottlenecks during transitions between hypo- and hyper-osmotic conditions. Both experimental and computational findings show that cells prioritize pathways that have higher thermodynamic driving force, like the pentose phosphate or the Entner–Doudoroff pathway, under low osmolarity. This work offers a systematic and mechanistic explanation for reduced growth rates in hypo- and hyper-osmotic conditions. The developed framework is the first of its kind to incorporate genome wide constraints that consider both natural logarithm and actual metabolite concentrations.Abstract Figure

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3