Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.

This study demonstrates the effects of simulated microgravity on E. coli K 12 MG1655 grown on LB medium supplemented with glycerol. Global gene expression analysis indicated that the expressions of hundred genes were significantly altered in simulated microgravity conditions compared to that of norm...

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Main Authors: Kotakonda Arunasri, Mohammed Adil, Katari Venu Charan, Chatterjee Suvro, Seerapu Himabindu Reddy, Sisinthy Shivaji
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3589462?pdf=render
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spelling doaj-cf96716a131a45f1a21e689e5f7f5d412020-11-25T01:29:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5786010.1371/journal.pone.0057860Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.Kotakonda ArunasriMohammed AdilKatari Venu CharanChatterjee SuvroSeerapu Himabindu ReddySisinthy ShivajiThis study demonstrates the effects of simulated microgravity on E. coli K 12 MG1655 grown on LB medium supplemented with glycerol. Global gene expression analysis indicated that the expressions of hundred genes were significantly altered in simulated microgravity conditions compared to that of normal gravity conditions. Under these conditions genes coding for adaptation to stress are up regulated (sufE and ssrA) and simultaneously genes coding for membrane transporters (ompC, exbB, actP, mgtA, cysW and nikB) and carbohydrate catabolic processes (ldcC, ptsA, rhaD and rhaS) are down regulated. The enhanced growth in simulated gravity conditions may be because of the adequate supply of energy/reducing equivalents and up regulation of genes involved in DNA replication (srmB) and repression of the genes encoding for nucleoside metabolism (dfp, pyrD and spoT). In addition, E. coli cultured in LB medium supplemented with glycerol (so as to protect the cells from freezing temperatures) do not exhibit multiple stress responses that are normally observed when cells are exposed to microgravity in LB medium without glycerol.http://europepmc.org/articles/PMC3589462?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kotakonda Arunasri
Mohammed Adil
Katari Venu Charan
Chatterjee Suvro
Seerapu Himabindu Reddy
Sisinthy Shivaji
spellingShingle Kotakonda Arunasri
Mohammed Adil
Katari Venu Charan
Chatterjee Suvro
Seerapu Himabindu Reddy
Sisinthy Shivaji
Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.
PLoS ONE
author_facet Kotakonda Arunasri
Mohammed Adil
Katari Venu Charan
Chatterjee Suvro
Seerapu Himabindu Reddy
Sisinthy Shivaji
author_sort Kotakonda Arunasri
title Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.
title_short Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.
title_full Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.
title_fullStr Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.
title_full_unstemmed Effect of simulated microgravity on E. coli K12 MG1655 growth and gene expression.
title_sort effect of simulated microgravity on e. coli k12 mg1655 growth and gene expression.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description This study demonstrates the effects of simulated microgravity on E. coli K 12 MG1655 grown on LB medium supplemented with glycerol. Global gene expression analysis indicated that the expressions of hundred genes were significantly altered in simulated microgravity conditions compared to that of normal gravity conditions. Under these conditions genes coding for adaptation to stress are up regulated (sufE and ssrA) and simultaneously genes coding for membrane transporters (ompC, exbB, actP, mgtA, cysW and nikB) and carbohydrate catabolic processes (ldcC, ptsA, rhaD and rhaS) are down regulated. The enhanced growth in simulated gravity conditions may be because of the adequate supply of energy/reducing equivalents and up regulation of genes involved in DNA replication (srmB) and repression of the genes encoding for nucleoside metabolism (dfp, pyrD and spoT). In addition, E. coli cultured in LB medium supplemented with glycerol (so as to protect the cells from freezing temperatures) do not exhibit multiple stress responses that are normally observed when cells are exposed to microgravity in LB medium without glycerol.
url http://europepmc.org/articles/PMC3589462?pdf=render
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