Difference between revisions of "PMID:23452849"
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!|Phenotype of!!Taxon Information!!Genotype Information (if known)!!Condition Information!!OMP ID!!OMP Term Name!!ECO ID!!ECO Term Name!!Notes!!Status | !|Phenotype of!!Taxon Information!!Genotype Information (if known)!!Condition Information!!OMP ID!!OMP Term Name!!ECO ID!!ECO Term Name!!Notes!!Status | ||
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+ | a mutation or genetic difference within a strain | ||
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+ | *Taxon: Escherichia coli | ||
+ | *Strain: K-12 | ||
+ | *Substrain: LR2 | ||
+ | *NCBI Taxon ID: [http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=83333&lvl=3&lin=f&keep=1&srchmode=1&unlock 83333] | ||
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+ | *Genotype of Reference Strain: LR2 | ||
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+ | *Reference Condition: | ||
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+ | repression of the murE-B operon allowed vigorous L-form growth. | ||
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Latest revision as of 18:25, 8 November 2013
Citation |
Mercier, R, Kawai, Y and Errington, J (2013) Excess membrane synthesis drives a primitive mode of cell proliferation. Cell 152:997-1007 |
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Abstract |
The peptidoglycan cell wall is a hallmark of the bacterial subkingdom. Surprisingly, many modern bacteria retain the ability to switch into a wall-free state called the L-form. L-form proliferation is remarkable in being independent of the normally essential FtsZ-based division machinery and in occurring by membrane blebbing and tubulation. We show that mutations leading to excess membrane synthesis are sufficient to drive L-form division in Bacillus subtilis. Artificially increasing the cell surface area to volume ratio in wild-type protoplasts generates similar shape changes and cell division. Our findings show that simple biophysical processes could have supported efficient cell proliferation during the evolution of early cells and provide an extant biological model for studying this problem. |
Links |
PubMed Online version:10.1016/j.cell.2013.01.043 |
Keywords |
Bacillus subtilis/cytology; Bacillus subtilis/metabolism; Bacterial Proteins/genetics; Bacterial Proteins/metabolism; Cell Division; Cell Membrane/metabolism; Cell Proliferation; Cell Wall/metabolism; Fatty Acid Synthetase Complex/genetics; Fatty Acid Synthetase Complex/metabolism; L Forms/cytology; L Forms/metabolism; Malonyl Coenzyme A/metabolism; Membrane Proteins/genetics; Membrane Proteins/metabolism; Peptidoglycan/metabolism; Polymorphism, Single Nucleotide; Protoplasts/metabolism |
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Main Points of the Paper
Please summarize the main points of the paper.
Materials and Methods Used
Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).
Phenotype Annotations
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Phenotype of | Taxon Information | Genotype Information (if known) | Condition Information | OMP ID | OMP Term Name | ECO ID | ECO Term Name | Notes | Status |
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a mutation or genetic difference within a strain |
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repression of the murE-B operon allowed vigorous L-form growth. |
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Notes
References
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