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1.
Chem Biol ; 7(8): 611-21, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11048952

ABSTRACT

BACKGROUND: Agrobacterium tumefaciens has been successfully harnessed as the only natural vector for the incorporation of foreign genes into higher plants, but its use in the grain crops is often limited. Low transformation efficiency has been partly attributed to a failure in the initial events in the transformation process, specifically in the capacity of the VirA/VirG two-component system to induce expression of the virulence genes. RESULTS: Here we show that the root exudate of Zea mays seedlings specifically inhibits virulence gene expression, determine that 2-hydroxy-4,7-dimethoxybenzoxazin-3-one (MDIBOA), which constitutes > 98% of the organic exudate of the roots of these seedlings, is the most potent and specific inhibitor of signal perception in A. tumefaciens-mediated gene transfer yet discovered, and develop a model that is able to predict the MDIBOA concentration at any distance from the root surface. Finally, variants of A. tumefaciens resistant to MDIBOA-mediated inhibition of vir gene expression have been selected and partially characterized. CONCLUSIONS: These results suggest a strategy in which a plant may resist pathogen invasion by specifically blocking virulence gene activation and yet ensure that the 'resistance factor' does not accumulate to levels sufficient to impose toxicity and selection pressure on the pathogen. The data further establish that naturally occurring inhibitors directed against signal perception by the VirA/VirG two-component regulatory system can play an important role in host defense. Finally, selected variants resistant to specific MDIBOA inhibition may now be used to extend the transformation efficiency of maize and possibly other cereals.


Subject(s)
Agrobacterium tumefaciens/drug effects , Agrobacterium tumefaciens/pathogenicity , Oxazines/pharmacology , Transformation, Genetic/drug effects , Virulence Factors , Zea mays/genetics , Zea mays/microbiology , Agrobacterium tumefaciens/genetics , Anti-Bacterial Agents/analysis , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Bacterial Proteins/genetics , Benzoxazines , Coculture Techniques , Diffusion , Dose-Response Relationship, Drug , Drug Resistance, Microbial/genetics , Gene Expression Regulation, Bacterial/drug effects , Genes, Reporter , Mutation/genetics , Oxazines/analysis , Oxazines/chemistry , Plant Roots/chemistry , Plant Roots/microbiology , Plants, Genetically Modified , Transcriptional Activation , Virulence/drug effects , Virulence/genetics , Zea mays/chemistry
2.
Chem Biol ; 5(2): 103-17, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9495831

ABSTRACT

BACKGROUND: The temporal and spatial control of the transition from vegetative to parasitic growth is critical to any parasite, but is essential to the sessile parasitic plants. It has been proposed that this transition in Striga spp. is controlled simply by an exuded oxidase that converts host cell-surface phenols into benzoquinones which act as developmental signals that mediate the transition. An understanding of this mechanism may identify the critical molecular events that made possible the evolution of parasitism in plants. RESULTS: PoxA and PoxB are identified as the only apoplastic phenol oxidases in Striga asiatica seedlings, and the genes encoding them have been cloned and sequenced. These peroxidase enzymes are capable of oxidizing the 60 known inducing phenols into a small set of benzoquinones, and it is these quinones that induce parasitic development. Analysis of the reaction requirements and comparisons to host enzymes, however, lead us to argue that PoxA and PoxB are not necessary for host recognition. CONCLUSIONS: A new model is proposed where constitutive production of an activated oxygen species (in the case of Striga, H2O2) mediates host recognition. This strategy would allow a parasite to exploit abundant host enzymes to produce the diffusible recognition signals by converting a standard host defense into a parasitic offense.


Subject(s)
Cell Wall/enzymology , Peroxidases/chemistry , Phenols/metabolism , Plants/parasitology , Amino Acid Sequence , Base Sequence , Benzoquinones/pharmacology , Cell Wall/chemistry , Cloning, Molecular , Conserved Sequence/genetics , Gallic Acid/analogs & derivatives , Gallic Acid/pharmacology , Gene Expression Regulation, Developmental/genetics , Histocytochemistry , Hydrogen-Ion Concentration , Molecular Sequence Data , Phylogeny , Plants/chemistry , RNA, Messenger/analysis , Seeds/cytology , Seeds/metabolism , Sequence Alignment , Sequence Analysis, DNA
3.
Bioorg Med Chem Lett ; 8(18): 2463-6, 1998 Sep 22.
Article in English | MEDLINE | ID: mdl-9873562

ABSTRACT

The program DOCK was used to search for novel inhibitors for alpha-thrombin. Four among the top twelve best scoring compounds from the Cambridge Structural Data Base inhibited this enzyme, and three of them inhibited alpha-thrombin in a competitive mode. These molecules are expected to serve as general templates for structural elaboration in targeting diverse serine proteases for selective inhibition.


Subject(s)
Drug Design , Serine Proteinase Inhibitors/chemical synthesis , Software , Thrombin/antagonists & inhibitors , Binding Sites , Databases, Factual , Models, Chemical , Models, Molecular , Protein Conformation , Templates, Genetic
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