| pubmed-article:20346349 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20346349 | lifeskim:mentions | umls-concept:C1624577 | lld:lifeskim |
| pubmed-article:20346349 | lifeskim:mentions | umls-concept:C0010383 | lld:lifeskim |
| pubmed-article:20346349 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
| pubmed-article:20346349 | lifeskim:mentions | umls-concept:C0443288 | lld:lifeskim |
| pubmed-article:20346349 | lifeskim:mentions | umls-concept:C1551359 | lld:lifeskim |
| pubmed-article:20346349 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:20346349 | pubmed:dateCreated | 2010-4-26 | lld:pubmed |
| pubmed-article:20346349 | pubmed:abstractText | The shape and compaction of the bacterial nucleoid may affect the accessibility of genetic material to the transcriptional machinery in natural and synthetic systems. To investigate this phenomenon, the nature and contribution of RNA and protein to the compaction of nucleoids that had been gently released from Escherichia coli cells were investigated using fluorescent and transmission electron microscopy. We propose that the removal of RNA from the bacterial nucleoid affects nucleoid compaction by altering the branching density and molecular weight of the nucleoid. We show that a common detergent in nucleoid preparations, Brij 58, plays a previously unrecognized role as a macromolecular crowding agent. RNA-free nucleoids adopt a compact structure similar in size to exponential-phase nucleoids when the concentration of Brij 58 is increased, consistent with our hypothesis. We present evidence that control and protein-free nucleoids behave similarly in solutions containing a macromolecular crowding agent. These results show that the contribution to DNA compaction by nucleoid-associated proteins is small when compared to macromolecular crowding effects. | lld:pubmed |
| pubmed-article:20346349 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20346349 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20346349 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20346349 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20346349 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20346349 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20346349 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20346349 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20346349 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20346349 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:20346349 | pubmed:issn | 1090-2104 | lld:pubmed |
| pubmed-article:20346349 | pubmed:author | pubmed-author:WilsonDavid... | lld:pubmed |
| pubmed-article:20346349 | pubmed:author | pubmed-author:ShulerMichael... | lld:pubmed |
| pubmed-article:20346349 | pubmed:author | pubmed-author:FoleyPatricia... | lld:pubmed |
| pubmed-article:20346349 | pubmed:copyrightInfo | 2010 Elsevier Inc. All rights reserved. | lld:pubmed |
| pubmed-article:20346349 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20346349 | pubmed:day | 23 | lld:pubmed |
| pubmed-article:20346349 | pubmed:volume | 395 | lld:pubmed |
| pubmed-article:20346349 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20346349 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20346349 | pubmed:pagination | 42-7 | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:meshHeading | pubmed-meshheading:20346349... | lld:pubmed |
| pubmed-article:20346349 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20346349 | pubmed:articleTitle | Macromolecular crowding can account for RNase-sensitive constraint of bacterial nucleoid structure. | lld:pubmed |
| pubmed-article:20346349 | pubmed:affiliation | School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853-5201, USA. | lld:pubmed |
| pubmed-article:20346349 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20346349 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:20346349 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
