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. 1999 Dec 7;96(25):14647-51.
doi: 10.1073/pnas.96.25.14647.

Herbicide sensitivity determinant of wheat plastid acetyl-CoA carboxylase is located in a 400-amino acid fragment of the carboxyltransferase domain

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Herbicide sensitivity determinant of wheat plastid acetyl-CoA carboxylase is located in a 400-amino acid fragment of the carboxyltransferase domain

T Nikolskaya et al. Proc Natl Acad Sci U S A. .

Abstract

A series of chimeral genes, consisting of the yeast GAL10 promoter, yeast ACC1 leader, wheat acetyl-CoA carboxylase (ACCase; EC 6.4.1.2) cDNA, and yeast ACC1 3'-tail, was used to complement a yeast ACC1 mutation. These genes encode a full-length plastid enzyme, with and without the putative chloroplast transit peptide, as well as five chimeric cytosolic/plastid proteins. Four of the genes, all containing at least half of the wheat cytosolic ACCase coding region at the 5'-end, complement the yeast mutation. Aryloxyphenoxypropionate and cyclohexanedione herbicides, at concentrations below 10 microM, inhibit the growth of haploid yeast strains that express two of the chimeric ACCases. This inhibition resembles the inhibition of wheat plastid ACCase observed in vitro and in vivo. The differential response to herbicides localizes the sensitivity determinant to the third quarter of the multidomain plastid ACCase. Sequence comparisons of different multidomain and multisubunit ACCases suggest that this region includes part of the carboxyltransferase domain, and therefore that the carboxyltransferase activity of ACCase (second half-reaction) is the target of the inhibitors. The highly sensitive yeast gene-replacement strains described here provide a convenient system to study herbicide interaction with the enzyme and a powerful screening system for new inhibitors.

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Figures

Figure 1
Figure 1
Chimeral genes constructed for expression of wheat cytosolic, plastid, and cytosolic/plastid ACCases in yeast. Construct names reflect composition of the encoded proteins (C, cytosolic ACCase, P, plastid ACCase). Locations of key restriction sites used in the constructions are shown. The major functional domains (biotin carboxylase and carboxyltransferase) and the biotin attachment sites are located as described before (3, 4).
Figure 2
Figure 2
Growth inhibition by herbicides of yeast gene-replacement haploid strains (Table 1) expressing chimeric wheat ACCases. Growth without herbicide in medium containing 1% DMSO, 100%. Average values for two strains containing the same construct obtained in two or three experiments are shown. Error bars indicate variation observed for each pair of strains. H, Haloxyfop; X, Cethoxydim, C, Clodinafop, P, Propaquizafop; Q, Quizalafop; S, Sethoxydim.

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