scholarly journals Porous assembly of an antifungal protein mediated by zinc and sulfonato-calix[8]arene

2021 ◽  
Vol 213 (2) ◽  
pp. 107711
Author(s):  
Francesca Guagnini ◽  
Anna Huber ◽  
Jimi M. Alex ◽  
Florentine Marx ◽  
Peter B. Crowley
Keyword(s):  
2001 ◽  
Vol 8 (3) ◽  
pp. 209-216 ◽  
Author(s):  
Hu Huang ◽  
Jin-fei Xu ◽  
Zhen-zhen Gong

2021 ◽  
Vol 9 (1) ◽  
pp. 140
Author(s):  
Ruying Wang ◽  
Simin Luo ◽  
Bruce B. Clarke ◽  
Faith C. Belanger

Strong creeping red fescue (Festuca rubra subsp. rubra) is a commercially important low-maintenance turfgrass and is often naturally infected with the fungal endophyte Epichloë festucae. Epichloë spp. are endophytes of several cool-season grass species, often conferring insect resistance to the grass hosts due to the production of toxic alkaloids. In addition to insect resistance, a unique feature of the strong creeping red fescue/E. festucae symbiosis is the endophyte-mediated disease resistance to the fungal pathogen Clarireedia jacksonii, the causal agent of dollar spot disease. Such disease resistance is not a general feature of other grass/ Epichloë interactions. E. festucae isolates infecting red fescue have an antifungal protein gene Efe-afpA, whereas most other Epichloë spp. do not have a similar gene. The uniqueness of this gene suggests it may, therefore, be a component of the unique disease resistance seen in endophyte-infected red fescue. Here, we report the generation of CRISPR-Cas9 Efe-afpA gene knockouts with the goal of determining if absence of the protein in endophyte-infected Festuca rubra leads to disease susceptibility. However, it was not possible to infect plants with the knockout isolates, although infection was possible with the wild type E. festucae and with complemented isolates. This raises the interesting possibility that, in addition to having antifungal activity, the protein is required for the symbiotic interaction. The antifungal protein is a small secreted protein with high expression in planta relative to its expression in culture, all characteristics consistent with effector proteins. If Efe-AfpA is an effector protein it must be specific to certain interactions, since most Epichloë spp. do not have such a gene in their genomes.


2009 ◽  
Vol 135 (1) ◽  
pp. 39-46 ◽  
Author(s):  
Raquel Acosta ◽  
Andrea Rodríguez-Martín ◽  
Alberto Martín ◽  
Félix Núñez ◽  
Miguel A. Asensio

2007 ◽  
Vol 55 (13) ◽  
pp. 5277-5281 ◽  
Author(s):  
Seong-Cheol Park ◽  
Jung Ro Lee ◽  
Sun-Oh Shin ◽  
Ji Hyun Jung ◽  
Young Mee Lee ◽  
...  

IUCrJ ◽  
2019 ◽  
Vol 6 (2) ◽  
pp. 238-247 ◽  
Author(s):  
Jimi M. Alex ◽  
Martin L. Rennie ◽  
Sylvain Engilberge ◽  
Gábor Lehoczki ◽  
Hajdu Dorottya ◽  
...  

Synthetic macrocycles such as calixarenes and cucurbiturils are increasingly applied as mediators of protein assembly and crystallization. The macrocycle can facilitate assembly by providing a surface on which two or more proteins bind simultaneously. This work explores the capacity of the sulfonato-calix[n]arene (sclx n ) series to effect crystallization of PAF, a small, cationic antifungal protein. Co-crystallization with sclx4, sclx6 or sclx8 led to high-resolution crystal structures. In the absence of sclx n , diffraction-quality crystals of PAF were not obtained. Interestingly, all three sclx n were bound to a similar patch on PAF. The largest and most flexible variant, sclx8, yielded a dimer of PAF. Complex formation was evident in solution via NMR and ITC experiments, showing more pronounced effects with increasing macrocycle size. In agreement with the crystal structure, the ITC data suggested that sclx8 acts as a bidentate ligand. The contributions of calixarene size/conformation to protein recognition and assembly are discussed. Finally, it is suggested that the conserved binding site for anionic calixarenes implicates this region of PAF in membrane binding, which is a prerequisite for antifungal activity.


1990 ◽  
Vol 136 (9) ◽  
pp. 1771-1778 ◽  
Author(s):  
W. K. Roberts ◽  
C. P. Selitrennikoff
Keyword(s):  

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