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	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Michaelis_menten_equation&amp;diff=11335</id>
		<title>Michaelis menten equation</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Michaelis_menten_equation&amp;diff=11335"/>
		<updated>2014-10-22T10:36:38Z</updated>

		<summary type="html">&lt;p&gt;130066442: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The Michaelis-Menten equation is used to work out the &#039;&#039;&#039;rate&#039;&#039;&#039; &#039;&#039;&#039;of [[Enzyme|enzyme]] reactions&#039;&#039;&#039; and is written as follows:&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp; V = &amp;lt;u&amp;gt;V&amp;lt;sub&amp;gt;max&amp;lt;/sub&amp;gt; [S]&amp;lt;/u&amp;gt;&amp;lt;br&amp;gt;&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp;&amp;amp;nbsp; K&amp;lt;sub&amp;gt;m&amp;lt;/sub&amp;gt; + [S]&#039;&#039;&#039;&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;V&#039;&#039;&#039;&amp;lt;sub&amp;gt;&#039;&#039;&#039;max&#039;&#039;&#039;&amp;lt;/sub&amp;gt; is the maximum rate of an [[Enzyme|enzyme]] reaction, occurs when all substrate is saturated.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;K&amp;lt;sub&amp;gt;m&amp;lt;/sub&amp;gt;&#039;&#039;&#039; is the Michaelis-Menten constant and is the substrate concentration at half V&amp;lt;sub&amp;gt;max&amp;amp;nbsp;&amp;lt;/sub&amp;gt;. (Higher the&amp;amp;nbsp;Km value, lower the affinity)&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&amp;lt;sub&amp;gt;&amp;lt;/sub&amp;gt;V&amp;lt;sub&amp;gt;max&amp;lt;/sub&amp;gt; and K&amp;lt;sub&amp;gt;m&amp;lt;/sub&amp;gt; can&amp;amp;nbsp;also be&amp;amp;nbsp;shown on a graph, the&amp;amp;nbsp;graph which shows this best is a&amp;amp;nbsp;&#039;&#039;&#039;double&amp;amp;nbsp;reciprocal plot &#039;&#039;&#039;([[Lineweaver-Burk|Lineweaver-Burk]] plot).&amp;amp;nbsp;You can&amp;amp;nbsp;obtain&amp;amp;nbsp;the results&amp;amp;nbsp;by plotting 1/V against 1/[S]&amp;amp;nbsp;&amp;lt;ref&amp;gt;Molecular Biology of the Cell, Alberts et al., 5th Edition (2007) Garland Science, New York Chapter 3 p162-163&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
=== References  ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;/div&gt;</summary>
		<author><name>130066442</name></author>
	</entry>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=F_plasmid&amp;diff=11334</id>
		<title>F plasmid</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=F_plasmid&amp;diff=11334"/>
		<updated>2014-10-22T10:34:17Z</updated>

		<summary type="html">&lt;p&gt;130066442: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The F plasmid is an example of a large [[Plasmid|plasmid]] which contains genes that allow the plasmids [[DNA|DNA]] to be transferred between cells. It is found in the bacterium [[E. coli|&#039;&#039;E. coli&#039;&#039;]]; [[E. coli|&#039;&#039;E. coli&#039;&#039;]] containing this F factor are known as F&amp;lt;sup&amp;gt;+ &amp;lt;/sup&amp;gt;and those without are known as F&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt;. The F stands for fertility and the F factor is around 100000 bases in length. The F&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; cells have a tube like structure called a [[Pilus|pilus]] which allows it to make contact with F&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; cells. This joining via a pilus in order to transfer DNA between bacteria&amp;amp;nbsp;is known as [[Reproduction by Conjugation|conjugation]]. Therefore the F plasmid is known as a [[Conjugative plasmid|conjugative plasmid]]. Within the&amp;amp;nbsp;[[E. coli|&#039;&#039;E. coli&#039;&#039;]] cells, the F plasmid has one or two copies making it a low-copy number plasmid. During the cell cycle, it replicates once and segregates to both daughter cells&amp;amp;nbsp;&amp;lt;ref&amp;gt;Information and ideas gained from chapter 9, pgs304-305, HartlL. and RuvoloM., (2011) Genetics: Analysis of Genes and Genomes, 8th Edition, Burlington, Jones &amp;amp;amp;amp;amp;amp;amp; Bartlett Learning.&amp;lt;/ref&amp;gt;.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
=== Transmission of the F plasmid.&amp;lt;br&amp;gt;  ===&lt;br /&gt;
&lt;br /&gt;
Within the F factor are genes which governs the maintenance and transmission of the F plasmid. As already mentioned, the F plasmid is transferred via [[Reproduction by Conjugation|conjugation]] which occurs due the [[Pilus|pilus]] known as the F pilus. All the proteins that are associated with the F pilus are [[Transcription|transcribed]] and [[Translation|translated]] from genes within the F factor. The F plasmid is not transferred to a F&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; cell via the F pilus, the F pilus merely pulls the two cells together allowing a [[Conjugative junction|conjugative junction]] to form which contains a pore that allows the DNA to pass from the F&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; cell to the F&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; cell. During transfer, the F plasmid unwinds and the outer strand breaks which will be the one that is transferred to the F&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; cell via the pore in the [[Conjugative junction|conjugative junction]]. Replication of the plasmid then takes place in order to make both single strands of DNA into double stranded DNA plasmids. In the original F&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; cell, the sigle strand merely undergoes [[Rolling circle replication|rolling circle replication]] to once again become double stranded. In the recipeint cell, the linear single stranded DNA&amp;amp;nbsp;is replicated into a double strand and becomes a circular F plasmid containing the F factor&amp;amp;nbsp;&amp;lt;ref&amp;gt;Information and Ideas gained from chapter 9, pgs304-305, HartlL. and RuvoloM. (2011) Genetics: Analysis of Genes and Genomes, 8th edition, Burlington, Jones &amp;amp;amp;amp;amp;amp;amp;amp; Bartlett Learning.&amp;lt;/ref&amp;gt;.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
Both &#039;&#039;[[E. coli|E. coli]]&#039;&#039; cells are now considered to be F&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; cells and therefore can both now transfer the F plasmid and therefore the F factor. This transfer only requires a few minutes although is not effiecent in natural conditions meaning only 10% of naturally occurring &#039;&#039;E. coli&#039;&#039; cells contain the F plasmid and hence the F factor&amp;amp;nbsp;&amp;lt;ref&amp;gt;Information and ideas gained from Chapter 9, pgs 304-305, HartlL. and RuvoloM.(2011)Genetics: Analysis of Genes and Genomes, 8th edition, Burlington, Jones &amp;amp;amp;amp;amp;amp;amp;amp; Bartlett Learning.&amp;lt;/ref&amp;gt;.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
NB: F plasmids are unusally large and can accept large scale inserts (up to 300kB)&amp;amp;nbsp;&lt;br /&gt;
&lt;br /&gt;
=== References:  ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;/div&gt;</summary>
		<author><name>130066442</name></author>
	</entry>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Plasmid&amp;diff=11333</id>
		<title>Plasmid</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Plasmid&amp;diff=11333"/>
		<updated>2014-10-22T10:32:54Z</updated>

		<summary type="html">&lt;p&gt;130066442: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Plasmids are [[Supercoiled|supercoiled]] [[DNA|DNA]] molecules present in most species of [[Bacteria|bacteria]]. These are not integrated into the host&amp;amp;nbsp;[[Chromosome|chromosome]] and are much smaller in length. &lt;br /&gt;
&lt;br /&gt;
Plasmids are not necessary for the survival of a [[Bacteria|bacteria]] but can contain [[Gene|genes]] that are advantageous in changing environmental conditions, an example would be [[Antibiotic resistance|antibiotic resistance]]&amp;amp;nbsp;[[Gene|genes]]&amp;amp;nbsp;&amp;lt;ref&amp;gt;Maloy  (1987), Microbial Genetics, 2nd edition, Jones and Bartlett Publishers.&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Plasmids have no replication machinery of their own and are reliant upon the host for duplication. &lt;br /&gt;
&lt;br /&gt;
Plasmids are very useful as vectors and in&amp;amp;nbsp;[[Recombinant DNA Technology|recombinant DNA techniques]]. Desired [[Genes|genes]] can be inserted in and amplified up. &lt;br /&gt;
&lt;br /&gt;
Examples of plasmids include the puC18, or the F plasmid. Note that the F plasmids are unusually large. This property allows large scale genetic exchange between bacteria.&amp;amp;nbsp;&lt;br /&gt;
&lt;br /&gt;
=== References  ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&amp;lt;br&amp;gt;&lt;/div&gt;</summary>
		<author><name>130066442</name></author>
	</entry>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Glutamic_acid&amp;diff=9980</id>
		<title>Glutamic acid</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Glutamic_acid&amp;diff=9980"/>
		<updated>2013-11-27T16:37:59Z</updated>

		<summary type="html">&lt;p&gt;130066442: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Glutamic acid (also known as [[Glutamate|Glutamate]]) is a negatively charged [[amino acid|amino acid]] with an [[acidic side chain|acidic side chain]]. It is a vital component in the excitatory pathways of the nervous system in mammals with it&#039;s [[gated ion channel|gated ion channels]] being the most common [[ion channels|ion channels]] found in the [[brain|brain]]. Glutamate ion channels found in the [[hippocampus|hippocampus]] are responsible for most of the depolarizing currents of [[Excitatory_postsynaptic_potential|Excitatory PostSynaptic Potentials]] (EPSPs)&amp;lt;ref&amp;gt;ALBERTS, B. (2008). Molecular biology of the cell. New York [etc.], Garland Science. p691&amp;lt;/ref&amp;gt;.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
===  ===&lt;br /&gt;
&lt;br /&gt;
Furthermore, Glutamic acid (Glutamate) is involved in Long Term Potentiation (LTP.) LTP is an example of synaptic plascitity. &amp;amp;nbsp;Glutamate is firstly released from the pre-synaptic neuron. Glutamate then binds to 2 inotropic receptors AMPA and NMDA (the NMDA at this point is currently blocked by magnesium ions though.)&amp;amp;nbsp;&lt;br /&gt;
&lt;br /&gt;
The AMPA receptor is a Na+ channel so an EPSP is triggers. The EPSP is converted to an action potential is the threshold value (-55mV) is reached. &amp;amp;nbsp;The depolarization caused as a result trigges the Mg2+ to be ejected from the NMDA receptor. This causes the NMDA receptor to open. As a result, Ca2+ ions flow through the NMDA receptor.&amp;amp;nbsp;&lt;br /&gt;
&lt;br /&gt;
The Ca2+ activates secondary messenger pathways, and so post-synaptic cell becomes more sensitive to glutamate. The release of Ca2+ causes enhanced neurotransmitter release (so enhanced glutatmate from the pre-synaptic cell.) For example, the Ca2+ can trigger a phorphorylation cascade, causing the phosphorylation of the glutamate receptor channels (AMPA and NMDA.)&amp;amp;nbsp;&lt;br /&gt;
&lt;br /&gt;
LTP leads to an increase in the quality (and quantity) of synaptic transmission.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=== References&amp;lt;br&amp;gt;  ===&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&amp;lt;u&amp;gt;&amp;lt;/u&amp;gt;&#039;&#039;&#039;(not mentioned). (2013). The Molecular Basis of Learning and Memory. Available: http://www.learner.org/courses/biology/textbook/neuro/neuro_9.html. Last accessed 27th November, 2013.&lt;/div&gt;</summary>
		<author><name>130066442</name></author>
	</entry>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Gram_negative&amp;diff=9947</id>
		<title>Gram negative</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Gram_negative&amp;diff=9947"/>
		<updated>2013-11-27T11:42:45Z</updated>

		<summary type="html">&lt;p&gt;130066442: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Bacteria are categorised into two main subgroups &#039;Gram negative&#039;&amp;amp;nbsp;and &#039;[[Gram positive]]&#039; bacteria (with the exception of&amp;amp;nbsp;[[Mycobacterium Tuberculosis]] which falls into neither of the two groups.) The Gram method of classification is dependent upon cell&amp;amp;nbsp;wall structure. In this article I am going to focus on the &#039;Gram negative&#039;&amp;amp;nbsp;wall structure. &lt;br /&gt;
&lt;br /&gt;
A Gram negative bacteria has a base lipid bi-layer similar to an [[Eukaryotic|eukaryotic]]&amp;amp;nbsp;plasma membrane, surrounded by the [[Periplasmic space|periplasmic space]]. A thin&amp;amp;nbsp;[[Peptidoglycan|peptidoglycan]] layer, much thinner in comparison&amp;amp;nbsp;to that of the gram positive bacteria then arises seperating the two periplasmic compartments.&amp;amp;nbsp;Peptidoglycan is a&amp;amp;nbsp;polymer made up of two repeating units of [[N-acetylmumaric acid|N-acetylmumaric acid and]] [[N-acetylglucosamine|N-acetylglucosamine which]] form linear chains due to cross linkages formed by the tetrapeptide side chains of the monomers. The outermost external barrier of a gram negative bacteria is a lipid like bi-layer, but this is highly disimilar from that of an eukaryotic plasma membrane. The inner leaflet of this outer membrane is studded with [[Lipoproteins|lipoproteins]] which associate to the [[Cytoskelton|cytoskelton]] and peptidoglycan layer. The outer leaflet is made up of [[LPS lipidpolysaccharide|LPS lipidpolysaccharide]]; composed of [[Lipid A|Lipid A]] a fucntional [[Endotoxin|endotoxin]] when released and an [[O polysacharide tail|O polysacharide tail]]. &lt;br /&gt;
&lt;br /&gt;
Due to the lipid characteristics of the outermost membrane of the cell wall the gram negative bacteria are stained pink when [[Gram staining|gram stained]]. &lt;br /&gt;
&lt;br /&gt;
Gram-negative refers to a classification of bacteria based upon their cell wall structure. Gram-negative bacteria appear red as a result of Gram testing, whereas Gram-positive stain purple. &lt;br /&gt;
&lt;br /&gt;
The structure of the Gram-negative bacterial cell wall is what distinguishes it from [[Gram positive|Gram-positive]] bacteria. Gram-negative bacteria contain a much thinner layer of [[Peptidoglycan|Peptidoglycan]] in comparison to a Gram-positive bacterial cell wall. The Gram-negative cell wall consists of a unique outer membrane, containing [[Lipopolysaccharides|lipopolysaccharides]], murein [[Lipoproteins|lipoproteins]] and porin channels. There is also a periplasmic space between the peptidoglycan cell wall, and the cell membrane. &lt;br /&gt;
&lt;br /&gt;
Gram-negative bacteria exhibit stronger resistance to Antibiotics such as [[Lysozyme|Lysozyme]] and pennicillin G, as well as greater resistance to dyes and detergents. The lipopolysaccharide consists of a core polysaccharide, Lipid A and O-antigen. This lipolysaccharide layer is important in excluding large hydrophobic susbstances from interacting with the cell. Lipid A attaches to the outer membrane ensuring that the lipopolysaccharide remains attached to the cell .&amp;lt;br&amp;gt;References&amp;lt;br&amp;gt;&lt;/div&gt;</summary>
		<author><name>130066442</name></author>
	</entry>
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