scispace - formally typeset
O

Ofir Ramot

Researcher at Hebrew University of Jerusalem

Publications -  6
Citations -  571

Ofir Ramot is an academic researcher from Hebrew University of Jerusalem. The author has contributed to research in topics: Trichoderma harzianum & Trichoderma. The author has an hindex of 5, co-authored 5 publications receiving 534 citations.

Papers
More filters
Journal ArticleDOI

Significance of lytic enzymes from Trichoderma spp. in the biocontrol of fungal plant pathogens

TL;DR: An overview is presented of the data currently available on lytic enzymes from the mycoparasitic fungus Trichoderma and effort is being aimed at improving biocontrol agents and plants by introducing Trichodma genes via genetic manipulations.
Journal ArticleDOI

Antifungal activity of a novel endochitinase gene (chit36) from Trichoderma harzianum Rifai TM.

TL;DR: A novel 36-kDa endochitinase named chit36 has been isolated and characterized from Trichoderma harzianum Rifai TM and completely inhibited the germination of Botrytis cinerea conidia.
Journal ArticleDOI

Expression regulation of the endochitinase chit36 from Trichoderma asperellum (T. harzianum T-203)

TL;DR: CHIT36 recombinant protein from the yeast Pichia pastoris was active against different phytopathogens, confirming the importance of this endochitinase in the mycoparasitic activity of Trichoderma antagonistic strains.
Journal ArticleDOI

Regulation of two homodimer hexosaminidases in the mycoparasitic fungus Trichoderma asperellum by glucosamine

TL;DR: Biochemical characterization, Edman degradation, and mass spectrometry demonstrated that EXC1Y and EXC2Y are both active as homodimers, both genes are up-regulated by glucosamine (GlcN), in contrast to two endochitinases of this fungus.
Journal ArticleDOI

Regulation of β-1,3-glucanase by carbon starvation in the mycoparasite Trichoderma harzianum

TL;DR: The β-1,3-glucanase system of the mycoparasitic T. harzianum, isolate T-Y, was found to be composed of at least five different enzymes, and their migration distance in acrylamide gels corresponded to peptides with molecular masses of 30–200 kDa, and they were named accordingly.