June
2001
, Volume
14
, Number
6
Pages
816
-
820
Authors
Venugopal
Valmeekam
,
1
Yen-Lin
Loh
,
2
and
Michael J. D.
San Francisco
2
Affiliations
1Department of Biological Sciences, Texas Tech University, Lubbock 79409, U.S.A.; 2Affymetrix, 6550 Vallejo Street, Emeryville, CA 94608, U.S.A.
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RelatedArticle
Accepted 20 February 2001.
Abstract
The negative regulatory protein ExuR in Erwinia chrysanthemi regulates expression of the galacturonate uptake (exuT) and utilization (uxaA, uxaB, uxaC) genes. We cloned and determined the nucleotide sequence of the exuR gene from E. chrysanthemi EC16. Analysis of the deduced amino acid sequence indicates that this protein possesses a helix-turn-helix motif and belongs to the GntR family of transcriptional repressors. Northern blot analysis and studies with transcriptional fusions of exuT in wild-type and exuR mutant backgrounds indicate that exuT transcription is deregulated in the exuR strain in vivo and in planta. [14C]-galacturonic acid uptake was constitutively high under inducing and noninducing conditions in the exuR mutant. Maximal exuT transcription activity was observed within 8 h of bacterial inoculation into potato tubers, well before any visible symptoms of disease were detected. This suggests that ExuT transport activity in E. chrysanthemi is important in the early stages of disease development.
JnArticleKeywords
Additional keywords:
digalacturonate,
gene regulation,
pectin utilization,
plant disease.
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ArticleCopyright
© 2001 The American Phytopathological Society