Krebs cycle step 3: Difference between revisions

From Proteopedia
Jump to navigationJump to search
New page: <h2>Step three of the Krebs Cycle: Isocitrate Dehydrogenase</h2> Image:isocitrate_3.jpg <p>Figure: Formation of α-ketoglutarate</p> <p>Like the second step of the Krebs cycle, ...
 
No edit summary
 
(One intermediate revision by one other user not shown)
Line 1: Line 1:
<h2>Step three of the Krebs Cycle: Isocitrate Dehydrogenase</h2>
<h2>Step three of the Krebs Cycle: [[Isocitrate dehydrogenase]]</h2>


[[Image:isocitrate_3.jpg]]
[[Image:isocitrate_3.jpg]]
<p>Figure: Formation of &alpha;-ketoglutarate</p>
<p>Figure: Formation of &alpha;-ketoglutarate</p>


<p>Like the second step of the Krebs cycle, the third reaction (see Figure) is a two-step reaction sequence. In the first step,  
<p>Like the second step of the [[Citric Acid Cycle|Krebs cycle]], the third reaction (see Figure) is a two-step reaction sequence. In the first step,  
the secondary OH group of isocitrate (highlighted in yellow) is oxidised by the coenzyme NAD<sup>+</sup>, and a ketone is formed. At this point it becomes apparent why citrate was previously isomerised to isocitrate: Without  
the secondary OH group of isocitrate (highlighted in yellow) is oxidised by the coenzyme NAD<sup>+</sup>, and a ketone is formed. At this point it becomes apparent why citrate was previously isomerised to isocitrate: Without  
this step, the oxidation would not have taken place, since tertiary alcohols can not be oxidised. In the second step of the  
this step, the oxidation would not have taken place, since tertiary alcohols can not be oxidised. In the second step of the  
reaction, the intermediate product is decarboxylated and thus  CO<sub>2</sub> (in green) and   
reaction, the intermediate product is decarboxylated and thus  CO<sub>2</sub> (in green) and   
&alpha;-ketoglutarate, the salt of &alpha;-ketoglutaric acid, are released. With this step, the carbon chain is shortened for the first time because &alpha;-ketoglutarate has a C5 body. </p>
&alpha;-ketoglutarate, the salt of &alpha;-ketoglutaric acid, are released. With this step, the carbon chain is shortened for the first time because &alpha;-ketoglutarate has a C5 body. </p>

Latest revision as of 09:22, 18 December 2019

Step three of the Krebs Cycle: Isocitrate dehydrogenase

Figure: Formation of α-ketoglutarate

Like the second step of the Krebs cycle, the third reaction (see Figure) is a two-step reaction sequence. In the first step, the secondary OH group of isocitrate (highlighted in yellow) is oxidised by the coenzyme NAD+, and a ketone is formed. At this point it becomes apparent why citrate was previously isomerised to isocitrate: Without this step, the oxidation would not have taken place, since tertiary alcohols can not be oxidised. In the second step of the reaction, the intermediate product is decarboxylated and thus CO2 (in green) and α-ketoglutarate, the salt of α-ketoglutaric acid, are released. With this step, the carbon chain is shortened for the first time because α-ketoglutarate has a C5 body.

Proteopedia Page Contributors and Editors (what is this?)

Verena Pietzner, Alexander Berchansky, Jaime Prilusky