Rubisco and Crop Output

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==Modifying Rubisco to Improve Crop Output==
==Modifying Rubisco to Improve Crop Output==
<StructureSection load='1aus' size='340' side='right' caption='Caption for this structure' scene=''>
<StructureSection load='1aus' size='340' side='right' caption='Caption for this structure' scene=''>
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This is a default text for your page '''Rubisco crop output'''. Click above on '''edit this page''' to modify. Be careful with the &lt; and &gt; signs.
 
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You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.
 
== Function ==
== Function ==
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This enzyme, Rubisco, only works during the day, or when there is a light source, and is turned off at night when it is dark. Carbon dioxide is attached to the binding site which turns it off and then back on again.
This enzyme, Rubisco, only works during the day, or when there is a light source, and is turned off at night when it is dark. Carbon dioxide is attached to the binding site which turns it off and then back on again.
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<scene name='81/814059/Rubisco_activase/1'>Rubisco Activase</scene> is Rubisco’s “chaperone” or “regulator”. It turns Rubisco on and off based off of the amount of carbon intake. ATP is used by rubisco activase to change rubisco structurally, which turns it on and off. “The activase is now recognized to be a member of the AAA(+) family, whose members participate in macromolecular complexes that perform diverse chaperone-like functions. The conserved nucleotide-binding domain of AAA(+) family members appears to have a common fold that when applied to the activase is generally consistent with previous site-directed mutagenesis studies of the activase.” (Portis Jr.)
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<scene name='81/814059/Rubisco_activase/1'>Rubisco Activase</scene> or RCA is Rubisco’s “chaperone” or “regulator”. It turns Rubisco on and off based off of the amount of carbon intake. ATP is used by rubisco activase to change rubisco structurally, which turns it on and off. “The activase is now recognized to be a member of the AAA(+) family, whose members participate in macromolecular complexes that perform diverse chaperone-like functions. The conserved nucleotide-binding domain of AAA(+) family members appears to have a common fold that when applied to the activase is generally consistent with previous site-directed mutagenesis studies of the activase.” (Portis Jr.)

Revision as of 21:54, 1 May 2019

Modifying Rubisco to Improve Crop Output

Caption for this structure

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References

  1. 1.0 1.1 Sharwood RE. Engineering chloroplasts to improve Rubisco catalysis: prospects for translating improvements into food and fiber crops. New Phytol. 2017 Jan;213(2):494-510. doi: 10.1111/nph.14351. Epub 2016 Dec 9. PMID:27935049 doi:http://dx.doi.org/10.1111/nph.14351

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Emily T. Frankenreiter, Michal Harel

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