{"id":637,"date":"2017-04-16T02:54:35","date_gmt":"2017-04-16T02:54:35","guid":{"rendered":"https:\/\/pressbooks.hcfl.edu\/bio1\/chapter\/6-7-feedback-inhibition-in-metabolic-pathways\/"},"modified":"2025-08-29T18:00:00","modified_gmt":"2025-08-29T18:00:00","slug":"6-7-feedback-inhibition-in-metabolic-pathways","status":"publish","type":"chapter","link":"https:\/\/pressbooks.hcfl.edu\/bio1\/chapter\/6-7-feedback-inhibition-in-metabolic-pathways\/","title":{"raw":"Feedback Inhibition in Metabolic Pathways","rendered":"Feedback Inhibition in Metabolic Pathways"},"content":{"raw":"Molecules can regulate enzyme function in many ways. The major question remains, however: What are these molecules and where do they come from? Some are cofactors and coenzymes, as you have learned. What other molecules in the cell provide enzymatic regulation such as allosteric modulation, and competitive and non-competitive inhibition? Perhaps the most relevant sources of regulatory molecules, with respect to enzymatic cellular metabolism, are the products of the cellular metabolic reactions themselves. In a most efficient and elegant way, cells have evolved to use the products of their own reactions for feedback inhibition of enzyme activity. Feedback inhibition <\/strong>involves the use of a reaction product to regulate its own further production (Figure 11<\/strong>). The cell responds to an abundance of the products by slowing down production during anabolic or catabolic reactions. Such reaction products may inhibit the enzymes that catalyzed their production through the mechanisms described above.\n\n[caption id=\"attachment_636\" align=\"alignnone\" width=\"1024\"]\"\" Figure 11 Metabolic pathways are a series of reactions catalyzed by multiple enzymes. Feedback inhibition, where the end product of the pathway inhibits an upstream process, is an important regulatory mechanism in cells.[\/caption]\n\nThe production of both amino acids and nucleotides is controlled through feedback inhibition. Additionally, ATP is an allosteric regulator of some of the enzymes involved in the catabolic breakdown of sugar, the process that creates ATP. In this way, when ATP is in abundant supply, the cell can prevent the production of ATP. On the other hand, ADP serves as a positive allosteric regulator (an allosteric activator) for some of the same enzymes that are inhibited by ATP. Thus, when relative levels of ADP are high compared to ATP, the cell is triggered to produce more ATP through sugar catabolism.\n

References<\/h1>\nUnless otherwise noted, images on this page are licensed under CC-BY 4.0<\/a>\u00a0by\u00a0OpenStax<\/a>.\n\nText adapted from: OpenStax<\/span>, Concepts of Biology. OpenStax CNX. May 18, 2016 http:\/\/cnx.org\/contents\/b3c1e1d2-839c-42b0-a314-e119a8aafbdd@9.10","rendered":"

Molecules can regulate enzyme function in many ways. The major question remains, however: What are these molecules and where do they come from? Some are cofactors and coenzymes, as you have learned. What other molecules in the cell provide enzymatic regulation such as allosteric modulation, and competitive and non-competitive inhibition? Perhaps the most relevant sources of regulatory molecules, with respect to enzymatic cellular metabolism, are the products of the cellular metabolic reactions themselves. In a most efficient and elegant way, cells have evolved to use the products of their own reactions for feedback inhibition of enzyme activity. Feedback inhibition <\/strong>involves the use of a reaction product to regulate its own further production (Figure 11<\/strong>). The cell responds to an abundance of the products by slowing down production during anabolic or catabolic reactions. Such reaction products may inhibit the enzymes that catalyzed their production through the mechanisms described above.<\/p>\n

\"\"
Figure 11 Metabolic pathways are a series of reactions catalyzed by multiple enzymes. Feedback inhibition, where the end product of the pathway inhibits an upstream process, is an important regulatory mechanism in cells.<\/figcaption><\/figure>\n

The production of both amino acids and nucleotides is controlled through feedback inhibition. Additionally, ATP is an allosteric regulator of some of the enzymes involved in the catabolic breakdown of sugar, the process that creates ATP. In this way, when ATP is in abundant supply, the cell can prevent the production of ATP. On the other hand, ADP serves as a positive allosteric regulator (an allosteric activator) for some of the same enzymes that are inhibited by ATP. Thus, when relative levels of ADP are high compared to ATP, the cell is triggered to produce more ATP through sugar catabolism.<\/p>\n

References<\/h1>\n

Unless otherwise noted, images on this page are licensed under CC-BY 4.0<\/a>\u00a0by\u00a0OpenStax<\/a>.<\/p>\n

Text adapted from: OpenStax<\/span>, Concepts of Biology. OpenStax CNX. May 18, 2016 http:\/\/cnx.org\/contents\/b3c1e1d2-839c-42b0-a314-e119a8aafbdd@9.10<\/p>\n","protected":false},"author":130,"menu_order":7,"template":"","meta":{"pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":["lisa-bartee-xj76dny2ij","shriner-waiter-je82lehkfk","catherine-creech-j8t7v8goe4"],"pb_section_license":"cc-by"},"chapter-type":[],"contributor":[82,80,81],"license":[53],"class_list":["post-637","chapter","type-chapter","status-publish","hentry","contributor-catherine-creech-j8t7v8goe4","contributor-lisa-bartee-xj76dny2ij","contributor-shriner-waiter-je82lehkfk","license-cc-by"],"part":610,"_links":{"self":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/637","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/users\/130"}],"version-history":[{"count":1,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/637\/revisions"}],"predecessor-version":[{"id":638,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/637\/revisions\/638"}],"part":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/parts\/610"}],"metadata":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapters\/637\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/media?parent=637"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/pressbooks\/v2\/chapter-type?post=637"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/contributor?post=637"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.hcfl.edu\/bio1\/wp-json\/wp\/v2\/license?post=637"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}