Skip to main content Accessibility help
×
Hostname: page-component-5c6d5d7d68-7tdvq Total loading time: 0 Render date: 2024-08-18T11:47:18.025Z Has data issue: false hasContentIssue false

4 - From simple periodic behaviour to complex oscillations, including bursting and chaos

Published online by Cambridge University Press:  26 February 2010

Albert Goldbeter
Affiliation:
Université Libre de Bruxelles
Get access

Summary

A biochemical model with two instability mechanisms

In the two-variable models studied for glycolytic oscillations and birhythmicity, periodic behaviour originates from a unique instability mechanism based on the autocatalytic regulation of an allosteric enzyme by its reaction product. The question arises as to what happens when two instability-generating mechanisms are present and coupled within the same system: can new modes of dynamic behaviour arise from such an interaction?

An example of such a situation was considered at the end of the preceding chapter: the system with two oscillatory isozymes (fig. 3.23) contains two instability mechanisms coupled in parallel. Compared with the model based on a single product-activated enzyme, new behavioural modes may be observed, such as birhythmicity, hard excitation and multiple oscillatory domains as a function of a control parameter. The modes of dynamic behaviour in that model remain, however, limited, because it contains only two variables. For complex oscillations such as bursting or chaos to occur, it is necessary that the system contain at least three variables.

The coupling in series of two enzyme reactions with autocatalytic regulation (fig. 4.1) permits the construction of a three-variable biochemical prototype containing two instability-generating mechanisms (Decroly, 1987a,b; Decroly & Goldbeter, 1982). As in the model for glycolytic oscillations, the substrate S of the first enzyme is introduced at a constant rate into the system; this substrate is transformed by enzyme E1 into product P1, which serves as substrate for a second enzyme E2 that transforms P1 into P2. The two allosteric enzymes are both activated by their reaction product; P1 and P2 are thus positive effectors of enzymes Ex and E2, respectively.

Type
Chapter
Information
Biochemical Oscillations and Cellular Rhythms
The Molecular Bases of Periodic and Chaotic Behaviour
, pp. 118 - 160
Publisher: Cambridge University Press
Print publication year: 1996

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×