The thermodynamic efficiency of computations made in cells across the range of life

Author:

Kempes Christopher P.1,Wolpert David123,Cohen Zachary4,Pérez-Mercader Juan5

Affiliation:

1. The Santa Fe Institute, 1399 Hyde Park Road, Santa Fe, NM 87501, USA

2. Department of Physics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

3. Beyond Center, Arizona State University, Tempe, AZ 85287, USA

4. Department of Biology, University of Illinois, Urbana Champagne, Urbana, IL 61801, USA

5. Department of Earth and Planetary Sciences, Harvard University, Cambridge, MA 02138, USA

Abstract

Biological organisms must perform computation as they grow, reproduce and evolve. Moreover, ever since Landauer’s bound was proposed, it has been known that all computation has some thermodynamic cost—and that the same computation can be achieved with greater or smaller thermodynamic cost depending on how it is implemented. Accordingly an important issue concerning the evolution of life is assessing the thermodynamic efficiency of the computations performed by organisms. This issue is interesting both from the perspective of how close life has come to maximally efficient computation (presumably under the pressure of natural selection), and from the practical perspective of what efficiencies we might hope that engineered biological computers might achieve, especially in comparison with current computational systems. Here we show that the computational efficiency of translation, defined as free energy expended per amino acid operation, outperforms the best supercomputers by several orders of magnitude, and is only about an order of magnitude worse than the Landauer bound. However, this efficiency depends strongly on the size and architecture of the cell in question. In particular, we show that the useful efficiency of an amino acid operation, defined as the bulk energy per amino acid polymerization, decreases for increasing bacterial size and converges to the polymerization cost of the ribosome. This cost of the largest bacteria does not change in cells as we progress through the major evolutionary shifts to both single- and multicellular eukaryotes. However, the rates of total computation per unit mass are non-monotonic in bacteria with increasing cell size, and also change across different biological architectures, including the shift from unicellular to multicellular eukaryotes. This article is part of the themed issue ‘Reconceptualizing the origins of life’.

Funder

Templeton World Charity Foundation

FQXi Foundation

U.S. National Science Foundation

Publisher

The Royal Society

Subject

General Physics and Astronomy,General Engineering,General Mathematics

Reference114 articles.

1. Transitions from nonliving to living matter;Rasmussen S;Proc. Natl Acad. Sci. USA,2010

2. Davies PEW Tuszynski JA Rieper E. 2013 Self-organization and entropy reduction in a living cell. Biosystems 111 1–10. (doi:10.1016/j.biosystems.2012.10.005)

3. Thermodynamics of natural selection I: Energy flow and the limits on organization

4. Thermodynamics of natural selection II: Chemical Carnot cycles

5. Thermodynamics of natural selection III: Landauer's principle in computation and chemistry

Cited by 42 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

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