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		<id>https://ecoliwiki.org/colipedia/index.php?title=PMID:6802799&amp;diff=1373895</id>
		<title>PMID:6802799</title>
		<link rel="alternate" type="text/html" href="https://ecoliwiki.org/colipedia/index.php?title=PMID:6802799&amp;diff=1373895"/>
		<updated>2012-12-08T16:21:03Z</updated>

		<summary type="html">&lt;p&gt;122.172.174.184: Fill PMID: Page!&lt;/p&gt;
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{|   id=&amp;quot;T50c368ef1dfdb&amp;quot;  class=&amp;quot; tableEdit PMID_info_table&amp;quot;  &lt;br /&gt;
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!align=left  |Citation&lt;br /&gt;
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&#039;&#039;&#039;Newman, EB, Malik, N and Walker, C&#039;&#039;&#039;  (1982) L-serine degradation in Escherichia coli K-12: directly isolated ssd mutants and their intragenic revertants.&#039;&#039;J. Bacteriol.&#039;&#039; &#039;&#039;&#039;150&#039;&#039;&#039;:710-5&lt;br /&gt;
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!align=left  |Abstract&lt;br /&gt;
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Two methods for the direct isolation of spontaneous ssd mutants of Escherichia coli K-12 strains are described; (i) by growth with L-serine as the carbon source, and (ii) by low-level kanamycin resistance. A newly isolated mutant had the same phenotype as the mutant described previously, including inefficient use of the glucose, inability to growth with succinate, altered transport characteristics, and altered resistance to certain growth effectors. Succinate-utilizing derivatives which appear to be intragenic are characterized in detail. The relation between the mutants isolated here and mutants which are thought to have impairment in a system of coupling respiratory energy to active transport (ecfB mutants) is discussed.&lt;br /&gt;
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;amp;db=pubmed&amp;amp;dopt=Abstract&amp;amp;list_uids=6802799 PubMed]&lt;br /&gt;
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Biological Transport, Active; Drug Resistance, Microbial; Escherichia coli; Genes, Bacterial; Glucose; Kanamycin; Mutation; Serine; Succinates; Succinic Acid&lt;br /&gt;
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==Significance {{HelpIcon|Help:Literature}} ==&lt;br /&gt;
{{LitSignificance}}&lt;br /&gt;
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== Useful Materials and Methods {{HelpIcon|Help:Literature}}==&lt;br /&gt;
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!|Gene product!!Qualifier!!GO ID!!GO term name!!Evidence Code!!with/from!!Aspect!!Notes!!Status&lt;br /&gt;
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&amp;lt;references/&amp;gt;&lt;/div&gt;</summary>
		<author><name>122.172.174.184</name></author>
	</entry>
	<entry>
		<id>https://ecoliwiki.org/colipedia/index.php?title=PMID:6802799&amp;diff=1373894</id>
		<title>PMID:6802799</title>
		<link rel="alternate" type="text/html" href="https://ecoliwiki.org/colipedia/index.php?title=PMID:6802799&amp;diff=1373894"/>
		<updated>2012-12-08T16:21:03Z</updated>

		<summary type="html">&lt;p&gt;122.172.174.184: New PMID: Page!&lt;/p&gt;
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		<author><name>122.172.174.184</name></author>
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	<entry>
		<id>https://ecoliwiki.org/colipedia/index.php?title=PMID:2185221&amp;diff=1373893</id>
		<title>PMID:2185221</title>
		<link rel="alternate" type="text/html" href="https://ecoliwiki.org/colipedia/index.php?title=PMID:2185221&amp;diff=1373893"/>
		<updated>2012-12-08T16:10:08Z</updated>

		<summary type="html">&lt;p&gt;122.172.174.184: Fill PMID: Page!&lt;/p&gt;
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{|   id=&amp;quot;S50c3665f9d86a&amp;quot;  class=&amp;quot; tableEdit PMID_info_table&amp;quot;  &lt;br /&gt;
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&#039;&#039;&#039;Rainwater, S and Silverman, PM&#039;&#039;&#039;  (1990) The Cpx proteins of Escherichia coli K-12: evidence that cpxA, ecfB, ssd, and eup mutations all identify the same gene.&#039;&#039;J. Bacteriol.&#039;&#039; &#039;&#039;&#039;172&#039;&#039;&#039;:2456-61&lt;br /&gt;
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An existing cpxA(Ts) mutant was resistant to amikacin at levels that inhibited completely the growth of a cpxA+ and a cpxA deletion strain and failed to grow as efficiently on exogenous proline. These properties are similar to those of mutants altered in a gene mapped to the cpxA locus and variously designated as ecfB, ssd, and eup. The amikacin resistance phenotype of the cpxA mutant was inseparable by recombination from the cpxA mutant phenotype (inability to grow at 41 degrees C without exogenous isoleucine and valine) and was recessive to the cpxA+ allele of a recombinant plasmid. Using methods that ensured independent mutations in the cpxA region of the chromosome, we isolated six new amikacin-resistant mutants following nitrosoguanidine mutagenesis. Three-factor crosses mapped the mutations to the cpxA locus. When transferred by P1 transduction to a cpxB11 Hfr strain, each of the mutations conferred the Tra- and Ilv- phenotypes characteristic of earlier cpxA mutants. Two of the new mutations led to a significantly impaired ability to utilize exogenous proline, and four led to partial resistance to colicin A. Two of the new cpxA alleles were recessive to the cpxA+ allele, and four were dominant, albeit to different degrees. On the basis of these data, we argue that cpxA, ecfB, eup, and ssd are all the same gene. We discuss the cellular function of the cpxA gene product in that light.&lt;br /&gt;
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;amp;db=pubmed&amp;amp;dopt=Abstract&amp;amp;list_uids=2185221 PubMed]&lt;br /&gt;
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Alleles; Amikacin; Bacterial Proteins; Colicins; Drug Resistance, Microbial; Escherichia coli; Genes, Bacterial; Genetic Linkage; Genotype; Mutation; Plasmids&lt;br /&gt;
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==Significance {{HelpIcon|Help:Literature}} ==&lt;br /&gt;
{{LitSignificance}}&lt;br /&gt;
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== Useful Materials and Methods {{HelpIcon|Help:Literature}}==&lt;br /&gt;
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&amp;lt;references/&amp;gt;&lt;/div&gt;</summary>
		<author><name>122.172.174.184</name></author>
	</entry>
	<entry>
		<id>https://ecoliwiki.org/colipedia/index.php?title=PMID:2185221&amp;diff=1373892</id>
		<title>PMID:2185221</title>
		<link rel="alternate" type="text/html" href="https://ecoliwiki.org/colipedia/index.php?title=PMID:2185221&amp;diff=1373892"/>
		<updated>2012-12-08T16:10:07Z</updated>

		<summary type="html">&lt;p&gt;122.172.174.184: New PMID: Page!&lt;/p&gt;
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		<author><name>122.172.174.184</name></author>
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