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PMID: 1846853 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Characterization of three Agrobacterium tumefaciens avirulent mutants with chromosomal mutations that affect induction of vir genes.

Journal of bacteriology ·Vol. 173 ·No. 3 ·1991-02-00 ·Pages 1080-7

Metts J, West J, Doares SH, Matthysse AG

Abstract

Three Agrobacterium tumefaciens mutants with chromosomal mutations that affect bacterial virulence were isolated by transposon mutagenesis. Two of the mutants were avirulent on all hosts tested. The third mutant, Ivr-211, was a host range mutant which was avirulent on Bryophyllum diagremontiana, Nicotiana tabacum, N. debneyi, N. glauca, and Daucus carota but was virulent on Zinnia elegans and Lycopersicon esculentum (tomato). That the mutant phenotype was due to the transposon insertion was determined by cloning the DNA containing the transposon insertion and using the cloned DNA to replace the wild-type DNA in the parent bacterial strain by marker exchange. The transposon insertions in the three mutants mapped at three widely separated locations on the bacterial chromosome. The effects of the mutations on various steps in tumor formation were examined. All three mutants showed no alteration in binding to carrot cells. However, none of the mutants showed any induction of vir genes by acetosyringone under conditions in which the parent strain showed vir gene induction. When the mutant bacteria were examined for changes in surface components, it was found that all three of the mutants showed a similar alteration in lipopolysaccharide (LPS). LPS from the mutants was larger in size and more heavily saccharide substituted than LPS from the parent strain. Two of the mutants showed no detectable alteration in outer membrane and periplasmic space proteins. The third mutant, Ivr-225, was missing a 79-kDa surface peptide. The reason(s) for the failure of vir gene induction in these mutants and its relationship, if any, to the observed alteration in LPS are unknown.

Related Genes
vir
MeSH Terms
Bacterial Proteins/analysis Chromosome Mapping Chromosomes, Bacterial Cloning, Molecular DNA Transposable Elements Electrophoresis, Polyacrylamide Gel Gene Expression Regulation, Bacterial Genes, Bacterial Lipopolysaccharides/analysis Membrane Proteins/analysis Mutagenesis, Insertional Mutation Phenotype Plants/microbiology Rhizobium/genetics Transcriptional Activation Virulence/genetics
Chemicals
Bacterial Proteins DNA Transposable Elements Lipopolysaccharides Membrane Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Metts J
Department of Biology, University of North Carolina, Chapel Hill 27599.
West J
Doares S H
Matthysse A G
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1991-02-00
Pages
1080-7
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC207227
Subset
IM
Grants
NCI NIH HHS · CA18604 · United States
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