Self-engineering capabilities of bacteria

Author:

Ben-Jacob Eshel12,Levine Herbert2

Affiliation:

1. School of Physics and Astronomy, Raymond and Beverly Sackler, Faculty of Exact Sciences, Tel-Aviv University69978 Tel-Aviv, Israel

2. Center for Theoretical Biological Physics, University of California at San DiegoLa Jolla, CA 92093-0319, USA

Abstract

Under natural growth conditions, bacteria can utilize intricate communication capabilities (e.g. quorum-sensing, chemotactic signalling and plasmid exchange) to cooperatively form (self-organize) complex colonies with elevated adaptability—the colonial pattern is collectively engineered according to the encountered environmental conditions. Bacteria do not genetically store all the information required for creating all possible patterns. Instead, additional information is cooperatively generated as required for the colonial self-organization to proceed. We describe how complex colonial forms (patterns) emerge through the communication-based singular interplay between individual bacteria and the colony. Each bacterium is, by itself, a biotic autonomous system with its own internal cellular informatics capabilities (storage, processing and assessment of information). These afford the cell plasticity to select its response to biochemical messages it receives, including self-alteration and the broadcasting of messages to initiate alterations in other bacteria. Hence, new features can collectively emerge during self-organization from the intracellular level to the whole colony. The cells thus assume newly co-generated traits and abilities that are not explicitly stored in the genetic information of the individuals.

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

Reference86 articles.

1. Bacterial Persistence as a Phenotypic Switch

2. Ball P The self-made tapestry—pattern formation in nature. 1999 Oxford:Oxford University Press.

3. MicroRNAs

4. Small Talk

5. Stress-Induced Mutagenesis in Bacteria

Cited by 105 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Evolution of predators and prey kills Turing patterns;2024-03-30

2. Emergence of collective adaptive response based on visual variation;Information Sciences;2024-01

3. Beauty;Proceedings of the ACM on Computer Graphics and Interactive Techniques;2023-08-12

4. Simulation of various biofilm fractal morphologies by agent-based model;Colloids and Surfaces B: Biointerfaces;2023-07

5. Rotating cluster formations emerge in an ensemble of active particles;Chaos, Solitons & Fractals;2023-07

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