scholarly journals Antifungal Activity of Rye (Secale cereale) Seed Chitinases: the Different Binding Manner of Class I and Class II Chitinases to the Fungal Cell Walls

2002 ◽  
Vol 66 (5) ◽  
pp. 970-977 ◽  
Author(s):  
Toki TAIRA ◽  
Takayuki OHNUMA ◽  
Takeshi YAMAGAMI ◽  
Yoichi ASO ◽  
Masatsune ISHIGURO ◽  
...  
2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Kátia Santana Cruz ◽  
Emerson Silva Lima ◽  
Marcia de Jesus Amazonas da Silva ◽  
Erica Simplício de Souza ◽  
Andreia Montoia ◽  
...  

Background. Cryptococcosis is a fungal disease of bad prognosis due to its pathogenicity and the toxicity of the drugs used for its treatment. The aim of this study was to investigate the medicinal potential of carbazole and β-carboline alkaloids and derivatives against Cryptococcus neoformans and C. gattii. Methods. MICs were established in accordance with the recommendations of the Clinical and Laboratory Standards Institute for alkaloids and derivatives against C. neoformans and C. gattii genotypes VNI and VGI, respectively. A single active compound was further evaluated against C. neoformans genotypes VNII, VNIII, and VNIV, C. gattii genotypes VGI, VGIII, and VGIV, Candida albicans ATCC 36232, for cytotoxicity against the MRC-5 lineage of human fibroblasts and for effects on fungal cells (cell wall, ergosterol, and leakage of nucleic acids). Results. Screening of 11 compounds revealed 8-nitroharmane as a significant inhibitor (MIC 40 μg/mL) of several C. neoformans and C. gattii genotypes. It was not toxic to fibroblasts (IC50 > 50 µg/mL) nor did it alter fungal cell walls or the concentration of ergosterol in C. albicans or C. neoformans. It increased leakage of substances that absorb at 260 nm. Conclusions. The synthetic β-carboline 8-nitroharmane significantly inhibits pathogenic Cryptococcus species and is interesting as a lead compound towards new therapy for Cryptococcus infections.


2001 ◽  
Vol 67 (12) ◽  
pp. 5833-5839 ◽  
Author(s):  
Hassane Ait-Lahsen ◽  
Andrés Soler ◽  
Manuel Rey ◽  
Jesús de la Cruz ◽  
Enrique Monte ◽  
...  

ABSTRACT Trichoderma harzianum secretes α-1,3-glucanases when it is grown on polysaccharides, fungal cell walls, or autoclaved mycelium as a carbon source (simulated antagonistic conditions). We have purified and characterized one of these enzymes, named AGN13.1. The enzyme was monomeric and slightly basic. AGN13.1 was an exo-type α-1,3-glucanase and showed lytic and antifungal activity against fungal plant pathogens. Northern and Western analyses indicated that AGN13.1 is induced by conditions that simulated antagonism. We propose that AGN13.1 contributes to the antagonistic response of T. harzianum.


1993 ◽  
Vol 39 (3) ◽  
pp. 318-328 ◽  
Author(s):  
Nicole Benhamou ◽  
Karen Broglie ◽  
Richard Broglie ◽  
Ilan Chet

A chitinase, purified to homogeneity from ethylene-treated bean leaves, was applied to actively growing mycelial cells of Rhizoctonia solani to evaluate a potential antifungal activity. Light microscopic investigations at 30-min intervals following enzyme exposure revealed the induction of morphological changes such as swelling of hyphal tips and hyphal distortions. More precise information concerning fungal cell alteration was obtained by ultrastructural observation and cytochemical detection of chitin distribution in fungal cell walls. Chitin breakdown was found to be an early event preceding wall disruption and cytoplasm leakage. The large amounts of chitin present in the walls of control R. solani cells and the rapid chitin hydrolysis upon chitinase treatment lead us to suggest that this polysaccharide is one of the main components of this fungal cell wall and is readily accessible to chitinase, especially in the apical zone. By 60 min after enzyme treatment, labeled molecules were observed in the vicinity of some fungal cells, suggesting the release of chitin oligosaccharides from fungal cell walls. The antifungal activity of the bean chitinase on cells of R. solani grown in culture is discussed in relation to the potential of genetically modified transgenic plants to resist attack by R. solani through an antimicrobial activity in planta.Key words: gold labeling, wheat germ agglutinin, cytochemistry, Rhizoctonia solani, bean endochitinase.


2018 ◽  
Vol 31 (5) ◽  
pp. 505-515 ◽  
Author(s):  
Hyo-Hyoun Seo ◽  
Ae Ran Park ◽  
Hyun-Hwa Lee ◽  
Sangkyu Park ◽  
Yun-Jeong Han ◽  
...  

Colletotrichum species are major fungal pathogens that cause devastating anthracnose diseases in many economically important crops. In this study, we observed the hydrolyzing activity of a fungus-inducible pepper carboxylesterase (PepEST) on cell walls of C. gloeosporioides, causing growth retardation of the fungus by blocking appressorium formation. To determine the cellular basis for the growth inhibition, we observed the localization of PepEST on the fungus and found the attachment of the protein on surfaces of conidia and germination tubes. Moreover, we examined the decomposition of cell-wall materials from the fungal surface after reaction with PepEST, which led to the identification of 1,2-dithiane-4,5-diol (DTD) by gas chromatography mass spectrometry analysis. Exogenous DTD treatment did not elicit expression of defense-related genes in the host plant but did trigger the necrosis of C. gloeosporioides. Furthermore, the DTD compound displayed protective effects on pepper fruits and plants against C. gloeosporioides and C. coccodes, respectively. In addition, DTD was also effective in preventing other diseases, such as rice blast, tomato late blight, and wheat leaf rust. Therefore, our results provide evidence that PepEST is involved in hydrolysis of the outmost layer of the fungal cell walls and that DTD has antifungal activity, suggesting an alternative strategy to control agronomically important phytopathogens.


The Analyst ◽  
2018 ◽  
Vol 143 (21) ◽  
pp. 5255-5263 ◽  
Author(s):  
Stephan Vogt ◽  
Marco Kelkenberg ◽  
Tanja Nöll ◽  
Benedikt Steinhoff ◽  
Holger Schönherr ◽  
...  

Chitin present in fungal cell walls has been considered as a diagnostic polymer for the detection of fungal infections.


1966 ◽  
Vol 42 (1) ◽  
pp. 39-42 ◽  
Author(s):  
R. MITCHELL ◽  
N. SABAR

1979 ◽  
Vol 71 (1) ◽  
pp. 51-64 ◽  
Author(s):  
Jaap Jelsma ◽  
Dirk R. Kreger

2020 ◽  
Vol 16 (1) ◽  
pp. e1007927 ◽  
Author(s):  
Ingrida Vendele ◽  
Janet A. Willment ◽  
Lisete M. Silva ◽  
Angelina S. Palma ◽  
Wengang Chai ◽  
...  

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