首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Increased cytoplasm viscosity hampers aggregate polar segregation in Escherichia coli
Authors:Samuel M D Oliveira  Ramakanth Neeli‐Venkata  Nadia S M Goncalves  João A Santinha  Leonardo Martins  Huy Tran  Jarno Mäkelä  Abhishekh Gupta  Marilia Barandas  Antti Häkkinen  Jason Lloyd‐Price  José M Fonseca  Andre S Ribeiro
Institution:1. Laboratory of Biosystem Dynamics, Department of Signal Processing, Tampere University of Technology, Tampere, Finland;2. UNINOVA, Instituto de Desenvolvimento de Novas Tecnologias, Campus FCT‐UNL, Caparica, Portugal
Abstract:In Escherichia coli, under optimal conditions, protein aggregates associated with cellular aging are excluded from midcell by the nucleoid. We study the functionality of this process under sub‐optimal temperatures from population and time lapse images of individual cells and aggregates and nucleoids within. We show that, as temperature decreases, aggregates become homogeneously distributed and uncorrelated with nucleoid size and location. We present evidence that this is due to increased cytoplasm viscosity, which weakens the anisotropy in aggregate displacements at the nucleoid borders that is responsible for their preference for polar localisation. Next, we show that in plasmolysed cells, which have increased cytoplasm viscosity, aggregates are also not preferentially located at the poles. Finally, we show that the inability of cells with increased viscosity to exclude aggregates from midcell results in enhanced aggregate concentration in between the nucleoids in cells close to dividing. This weakens the asymmetries in aggregate numbers between sister cells of subsequent generations required for rejuvenating cell lineages. We conclude that the process of exclusion of protein aggregates from midcell is not immune to stress conditions affecting the cytoplasm viscosity. The findings contribute to our understanding of E. coli's internal organisation and functioning, and its fragility to stressful conditions.
Keywords:
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号