Optimized bacteria are environmental prediction engines

Experimentalists observe phenotypic variability even in isogenic bacteria populations. We explore the hypothesis that in fluctuating environments this variability is tuned to maximize a bacterium's expected log-growth rate, potentially aided by epigenetic (all inheritable nongenetic) markers th...

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Main Authors: Marzen, Sarah E., Crutchfield, James P.
Other Authors: Massachusetts Institute of Technology. Department of Physics
Format: Article
Language:English
Published: American Physical Society 2018
Online Access:http://hdl.handle.net/1721.1/117060
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author Marzen, Sarah E.
Crutchfield, James P.
author2 Massachusetts Institute of Technology. Department of Physics
author_facet Massachusetts Institute of Technology. Department of Physics
Marzen, Sarah E.
Crutchfield, James P.
author_sort Marzen, Sarah E.
collection MIT
description Experimentalists observe phenotypic variability even in isogenic bacteria populations. We explore the hypothesis that in fluctuating environments this variability is tuned to maximize a bacterium's expected log-growth rate, potentially aided by epigenetic (all inheritable nongenetic) markers that store information about past environments. Crucially, we assume a time delay between sensing and action, so that a past epigenetic marker is used to generate the present phenotypic variability. We show that, in a complex, memoryful environment, the maximal expected log-growth rate is linear in the instantaneous predictive information—the mutual information between a bacterium's epigenetic markers and future environmental states. Hence, under resource constraints, optimal epigenetic markers are causal states—the minimal sufficient statistics for prediction—or lossy approximations thereof. We propose new theoretical investigations into and new experiments on bacteria phenotypic bet-hedging in fluctuating complex environments.
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spelling mit-1721.1/1170602022-09-30T22:21:50Z Optimized bacteria are environmental prediction engines Marzen, Sarah E. Crutchfield, James P. Massachusetts Institute of Technology. Department of Physics Marzen, Sarah E. Experimentalists observe phenotypic variability even in isogenic bacteria populations. We explore the hypothesis that in fluctuating environments this variability is tuned to maximize a bacterium's expected log-growth rate, potentially aided by epigenetic (all inheritable nongenetic) markers that store information about past environments. Crucially, we assume a time delay between sensing and action, so that a past epigenetic marker is used to generate the present phenotypic variability. We show that, in a complex, memoryful environment, the maximal expected log-growth rate is linear in the instantaneous predictive information—the mutual information between a bacterium's epigenetic markers and future environmental states. Hence, under resource constraints, optimal epigenetic markers are causal states—the minimal sufficient statistics for prediction—or lossy approximations thereof. We propose new theoretical investigations into and new experiments on bacteria phenotypic bet-hedging in fluctuating complex environments. Templeton Foundation (Grant 52095) Foundational Questions Institute (Grant FQXi-RFP-1609) United States. Army Research Office (Contract W911NF-13-1-0390) 2018-07-24T13:43:54Z 2018-07-24T13:43:54Z 2018-07 2018-06 2018-07-16T18:00:16Z Article http://purl.org/eprint/type/JournalArticle 2470-0045 2470-0053 http://hdl.handle.net/1721.1/117060 Marzen, Sarah E. and Crutchfield, James P. "Optimized bacteria are environmental prediction engines." Physical Review E 98, 1 (July 2018): 012408 © 2018 American Physical Society en http://dx.doi.org/10.1103/PhysRevE.98.012408 Physical Review E Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. American Physical Society application/pdf American Physical Society American Physical Society
spellingShingle Marzen, Sarah E.
Crutchfield, James P.
Optimized bacteria are environmental prediction engines
title Optimized bacteria are environmental prediction engines
title_full Optimized bacteria are environmental prediction engines
title_fullStr Optimized bacteria are environmental prediction engines
title_full_unstemmed Optimized bacteria are environmental prediction engines
title_short Optimized bacteria are environmental prediction engines
title_sort optimized bacteria are environmental prediction engines
url http://hdl.handle.net/1721.1/117060
work_keys_str_mv AT marzensarahe optimizedbacteriaareenvironmentalpredictionengines
AT crutchfieldjamesp optimizedbacteriaareenvironmentalpredictionengines