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Laura R. Abad

Researcher at Purdue University

Publications -  6
Citations -  536

Laura R. Abad is an academic researcher from Purdue University. The author has contributed to research in topics: Trichoderma longibrachiatum & Hyphal growth. The author has an hindex of 6, co-authored 6 publications receiving 523 citations.

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Antifungal activity of tobacco osmotin has specificity and involves plasma membrane permeabilization

TL;DR: Osmotin either induced spore lysis, inhibited spore germination or reduced germling viability in seven fungal species that exhibited some degree of sensitivity in hyphal growth inhibition tests, suggesting that the cell wall may be a component of the mechanism by which osmotin permeabilizes the plasma membrane and kills fungal cells.
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Stress proteins on the yeast cell surface determine resistance to osmotin, a plant antifungal protein

TL;DR: It is demonstrated that fungal cell wall proteins are determinants of resistance to antifungal PR-5 proteins, indicating that the cell membrane interacts specifically with osmotin and facilitates its action.
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Novel osmotically induced antifungal chitinases and bacterial expression of an active recombinant isoform.

TL;DR: The purified recombinant protein exhibited antifungal activity comparable to a class I chitinase purified from NaCl-adapted tobacco cells.
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In vivo and in vitro activity of truncated osmotin that is secreted into the extracellular matrix

TL;DR: It is shown that transgenic tobacco and potato plants that overexpressed the truncated osmotin protein exhibited resistance to Phytophthora infestans and that in plants overexpressing a C-terminal 20 amino acid truncated Osmotin gene, osmoton was totally secreted into the extracellular matrix.
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Induction of pathogen resistance and pathogenesis‐related genes in tobacco by a heat‐stable Trichoderma mycelial extract and plant signal messengers

TL;DR: The results suggest that the signal transduction pathways for elicitation of defense responses by exogenously applied heat-stable nonpathogenic mycelial extract and SA/MeJA overlap at the point of PR protein induction but are not identical.