Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-r6qrq Total loading time: 0 Render date: 2024-04-27T15:50:31.094Z Has data issue: false hasContentIssue false

The genetics of aspartate derived amino acids in higher plants

Published online by Cambridge University Press:  09 April 2010

R. M. Wallsgrove
Affiliation:
Institute of arable Crops Research (IACR), Rothamsted, UK
Get access

Summary

Introduction

Although the central role of amino acid biosynthesis in plant metabolism and development is evident, progress in the understanding of the molecular mechanisms by which such pathways are regulated is only recent. To elucidate the genetic regulation of a pathway, mutants have proved to be invaluable in the analysis of microbial systems. The same is true for plants, but again there are only a few pathways for which mutants with defective or altered essential functions are available. However, the improvements in plant mutant isolation at cell and whole plant levels, and in molecular biology have now provided mutants affected in amino acid metabolism as well as amino acid biosynthetic genes or cDNAs (for a review, see Last, 1992).

The branched biosynthetic pathway of aspartate-derived amino acids (lysine, methionine, threonine) and the related pathway leading to isoleucine, valine and leucine have received much interest for various reasons. First, it gives rise to essential amino acids which, if poorly represented as lysine in cereals and methionine in legumes, limit the nutritional quality of crop plants as diet for human beings and monogastric animals. Secondly, three classes of potent herbicides (sulphonylureas, imidazolinones and triazolopyrimidin) kill plants through the inhibition of acetolactate synthase, an enzyme common to the isoleucine and valine pathways. Key regulatory enzymes of the aspartate-derived amino acid biosynthesis would also be suitable targets for efficient herbicides while little affecting the environment.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 1995

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
×