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In Vitro Binding of Agrobacterium tumefaciens to Plant Cells from Suspension Culture

TLDR
Autoradiographic analysis and electron micrographs clearly illustrated a tight association of virulent A. tumefaciens strain B6 cells to the Datura cell wall, and that often binding of bacteria was localized.
Abstract
In vitro binding experiments were carried out using 32P-labeled cells of the virulent Agrobacterium tumefaciens strain B6 and Datura innoxia cells from suspension culture. Binding kinetics showed that adherence of bacteria to Datura cells increased gradually during the first 60 minutes and attained a maximum level within 120 minutes of incubation. Maximum binding occurred at pH 6.0. The presence of Ca2+ and Mg2+ reduced binding slightly and EDTA had little effect at concentrations of 0.1 to 10 millimolar. The binding of bacteria to Datura cells was temperature-dependent. Escherichia coli, Salmonella typhimurium, Rhizobium japonicum, and Micrococcus lysodeikticus did not compete with virulent A. tumefaciens strain B6 for binding to Datura cells. The admixture of avirulent A. tumefaciens strain IIBNV6 enhanced adherence of virulent A. tumefaciens strain B6 to Datura cells. Octopine had no effect on the binding of virulent A. tumefaciens strain B6 to Datura cells, but 10 millimolar canavanine was inhibitory. Arginine enhanced the adherence of the bacteria at concentrations higher than 0.1 millimolar. Incubation with DNase, RNase, and lipase did not affect the binding, but protease stimulated the adherence of bacteria to Datura cells. Concanavaline A and soybean lectin had little effect whereas lecithin and lysolecithin enhanced binding slightly. Poly-l-lysine markedly stimulated the bacteria-plant cell adherence. Cells from suspension cultures of pea, vetch, and soybean had a 2- to 3-fold higher binding capacity than Datura cells, whereas cells from wheat, corn, rice, and sorghum had a considerably lower affinity for binding with virulent A. tumefaciens strain B6. Bacterial adherence to plant cells was confirmed by autoradiography and electron microscopy. Autoradiographic analysis showed that bacteria were associated with the cell wall, and that often binding of bacteria was localized. Electron micrographs clearly illustrated a tight association of virulent A. tumefaciens strain B6 cells to the Datura cell wall.

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Journal ArticleDOI

Identification and genetic analysis of an Agrobacterium tumefaciens chromosomal virulence region.

TL;DR: A cosmid clone of the chromosomal virulence region containing a lac fusion in the extreme 3' portion of the 5-kilobase locus was used to demonstrate that expression of this region is dependent on the presence of sequences in the 5' portions of the locus, confirming its operon-like nature.
Journal ArticleDOI

Signal exchange in plant-microbe interactions.

TL;DR: Resistance aux maladies vegetales, crown gall and Agrobacterium, and Symbiose Rhizobium-legumineuses.
Journal ArticleDOI

Elaboration of cellulose fibrils by Agrobacterium tumefaciens during attachment to carrot cells.

TL;DR: Bacterial attachment to heat-killed or glutaraldehyde-fixed carrot cells proceeded with only slightly altered kinetics and unaltered bacterial strain specificity and fibrils developed, surrounded the bacteria, and anchored them to the plant cell surface.
Journal ArticleDOI

Agrobacterium tumefaciens mutants affected in attachment to plant cells.

TL;DR: Six of eight avirulent mutants with Tn5 insertions in chromosomal DNA showed defective attachment, whereas two retained wild-type attachment ability, and the attachment-defective mutants failed to inhibit tumorigenesis when inoculated onto Jerusalem artichoke slices before inoculation of a virulent strain.
References
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Journal ArticleDOI

A revised medium for rapid growth and bio assays with tobacco tissue cultures

TL;DR: In vivo redox biosensing resolves the spatiotemporal dynamics of compartmental responses to local ROS generation and provide a basis for understanding how compartment-specific redox dynamics may operate in retrograde signaling and stress 67 acclimation in plants.
Journal ArticleDOI

Large plasmid in Agrobacterium tumefaciens essential for crown gall-inducing ability

TL;DR: The hypothesis that the genetic information for the tumour-inducing principle in crown gall-inducing Agrobacterium strains is carried by one or several large plasmids is formulated.
Journal ArticleDOI

Supercoiled circular DNA in crown-gall inducing Agrobacterium strains

TL;DR: The hypothesis is formulated that the large plasmid present in crown-gall inducing bacteria could be the “tumor-inducing principle”.
Journal ArticleDOI

Octopine and nopaline synthesis and breakdown genetically controlled by a plasmid of Agrobacterium tumefaciens

TL;DR: Several nopaline degrading strains and one octopine degrading strain are shown to loose oncogenicity as well as the ability to utilize these guanidine compounds when they are cured of their TI plasmid.
Journal ArticleDOI

Bacterial Attachment to a Specific Wound Site as an Essential Stage in Tumor Initiation by Agrobacterium tumefaciens

TL;DR: The data fit a one-particle dose response curve, which indicates that a single IIBNV6 cell can prevent tumor initiation by a single B6 cell, and a specific complementary binding of a virulent bacterium to a host wound site exposed by the inoculation procedure is suggested as an essential early event in the crown-gall tumor initiation process.
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