scholarly journals An emerging role of pectic rhamnogalacturonanII for cell wall integrity

2012 ◽  
Vol 7 (2) ◽  
pp. 298-299 ◽  
Author(s):  
Rebecca Reboul ◽  
Raimund Tenhaken
Keyword(s):  
Cell Wall ◽  
Cell Wall Integrity

scholarly journals To preserve or to destroy, that is the question: the role of the cell wall integrity pathway in pollen tube growth

2019 ◽  
Vol 52 ◽  
pp. 131-139 ◽  
Author(s):  
Hannes Vogler ◽  
Gorka Santos-Fernandez ◽  
Martin A Mecchia ◽  
Ueli Grossniklaus
Keyword(s):  
Cell Wall ◽  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Cell Wall Integrity ◽  
Tube Growth ◽  
Cell Wall Integrity Pathway

scholarly journals SUN-Family Protein UvSUN1 Regulates the Development and Virulence of Ustilaginoidea virens

2021 ◽  
Vol 12 ◽  
Author(s):  
Mina Yu ◽  
Junjie Yu ◽  
Huijuan Cao ◽  
Tianqiao Song ◽  
Xiayan Pan ◽  
...  
Keyword(s):  
Cell Wall ◽  
Hyphal Growth ◽  
Cell Wall Integrity ◽  
Signal Recognition ◽  
Phenotypic Analysis ◽  
Ustilaginoidea Virens ◽  
Group I ◽  
Family Protein ◽  
False Smut

Ustilaginoidea virens, the causal agent of rice false smut disease, is an important plant pathogen that causes severe quantitative and qualitative losses in rice worldwide. UvSUN1 is the only member of Group-I SUN family proteins in U. virens. In this work, the role of UvSUN1 in different aspects of the U. virens biology was studied by phenotypic analysis of Uvsun1 knockout strains. We identified that UvSUN1 was expressed during both conidial germination and the infection of rice. Disruption of the Uvsun1 gene affected the hyphal growth, conidiation, morphology of hyphae and conidia, adhesion and virulence. We also found that UvSUN1 is involved in the production of toxic compounds, which are able to inhibit elongation of the germinated seeds. Moreover, RNA-seq data showed that knockout of Uvsun1 resulted in misregulation of a subset of genes involved in signal recognition and transduction system, glycometabolism, cell wall integrity, and secondary metabolism. Collectively, this study reveals that Uvsun1 is required for growth, cell wall integrity and pathogenicity of U. virens, thereby providing new insights into the function of SUN family proteins in the growth and pathogenesis of this pathogen.

scholarly journals Differential Requirement for the Cell Wall Integrity Sensor Wsc1p in Diploids Versus Haploids

2021 ◽  
Vol 7 (12) ◽  
pp. 1049
Author(s):  
Allison E. Hall ◽  
Miriam Lisci ◽  
Mark D. Rose
Keyword(s):  
Cell Wall ◽  
Membrane Integrity ◽  
Wall Stress ◽  
Cell Wall Integrity ◽  
Primary Role ◽  
Stringent Requirement ◽  
Temperature Changes ◽  
Bud Emergence ◽  
Cell Wall Integrity Pathway

The primary role of the Cell Wall Integrity Pathway (CWI) in Saccharomyces cerevisiae is monitoring the state of the cell wall in response to general life cycle stresses (growth and mating) and imposed stresses (temperature changes and chemicals). Of the five mechanosensor proteins monitoring cell wall stress, Wsc1p and Mid2p are the most important. We find that WSC1 has a stringent requirement in zygotes and diploids, unlike haploids, and differing from MID2’s role in shmoos. Diploids lacking WSC1 die frequently, independent of mating type. Death is due to loss of cell wall and plasma membrane integrity, which is suppressed by osmotic support. Overexpression of several CWI pathway components suppress wsc1∆ zygotic death, including WSC2, WSC3, and BEM2, as well as the Rho-GAPS, BEM3 and RGD2. Microscopic observations and suppression by BEM2 and BEM3 suggest that wsc1∆ zygotes die during bud emergence. Downstream in the CWI pathway, overexpression of a hyperactive protein kinase C (Pkc1p-R398P) causes growth arrest, and blocks the pheromone response. With moderate levels of Pkc1p-R398P, cells form zygotes and the wsc1∆ defect is suppressed. This work highlights functional differences in the requirement for Wsc1p in diploids Versus haploids and between Mid2p and Wsc1p during mating.

scholarly journals Candida albicans cell wall integrity transcription factors regulate polymicrobial biofilm formation with Streptococcus gordonii

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7870 ◽  
Author(s):  
Jennifer Chinnici ◽  
Lisa Yerke ◽  
Charlene Tsou ◽  
Sujay Busarajan ◽  
Ryan Mancuso ◽  
...  
Keyword(s):  
Cell Wall ◽  
Candida Albicans ◽  
Transcription Factors ◽  
Biofilm Formation ◽  
Mixed Cultures ◽  
Cell Wall Integrity ◽  
Antibiotic Tolerance ◽  
Streptococcus Gordonii ◽  
Knock Out

Polymicrobial biofilms play important roles in oral and systemic infections. The oral plaque bacterium Streptococcus gordonii is known to attach to the hyphal cell wall of the fungus Candida albicans to form corn-cob like structures in biofilms. However, the role of C. albicans in formation of polymicrobial biofilms is not completely understood. The objective of this study was to determine the role of C. albicans transcription factors in regulation of polymicrobial biofilms and antibiotic tolerance of S. gordonii. The proteins secreted by C. albicans and S. gordonii in mixed planktonic cultures were determined using mass spectrometry. Antibiotic tolerance of S. gordonii to ampicillin and erythromycin was determined in mixed cultures and mixed biofilms with C. albicans. Additionally, biofilm formation of S. gordonii with C. albicans knock-out mutants of 45 transcription factors that affect cell wall integrity, filamentous growth and biofilm formation was determined. Furthermore, these mutants were also screened for antibiotic tolerance in mixed biofilms with S. gordonii. Analysis of secreted proteomes resulted in the identification of proteins being secreted exclusively in mixed cultures. Antibiotic testing showed that S. gordonii had significantly increased survival in mixed planktonic cultures with antibiotics as compared to single cultures. C. albicans mutants of transcription factors Sfl2, Brg1, Leu3, Cas5, Cta4, Tec1, Tup1, Rim101 and Efg1 were significantly affected in mixed biofilm formation. Also mixed biofilms of S. gordonii with mutants of C. albicans transcription factors, Tec1 and Sfl2, had significantly reduced antibiotic tolerance as compared to control cultures. Our data indicates that C. albicans may have an important role in mixed biofilm formation as well as antibiotic tolerance of S. gordonii in polymicrobial biofilms. C. albicans may play a facilitating role than being just an innocent bystander in oral biofilms and infections.

scholarly journals Characterization of theStreptomyces coelicolorGlycoproteome Reveals Glycoproteins Important for Cell Wall Biogenesis

mBio ◽  
2019 ◽  
Vol 10 (3) ◽  
Author(s):  
Tessa Keenan ◽  
Adam Dowle ◽  
Rachel Bates ◽  
Margaret C. M. Smith
Keyword(s):  
Cell Wall ◽  
Abc Transporters ◽  
Streptomyces Coelicolor ◽  
Cell Wall Integrity ◽  
Enzyme Function ◽  
Cell Physiology ◽  
Cell Wall Biosynthesis ◽  
Content Type ◽  
Glycosylation Sites

ABSTRACTThe physiological role of protein O-glycosylation in prokaryotes is poorly understood due to our limited knowledge of the extent of their glycoproteomes. InActinobacteria, defects in protein O-mannosyl transferase (Pmt)-mediated protein O-glycosylation have been shown to significantly retard growth (Mycobacterium tuberculosisandCorynebacterium glutamicum) or result in increased sensitivities to cell wall-targeting antibiotics (Streptomyces coelicolor), suggesting that protein O-glycosylation has an important role in cell physiology. Only a single glycoprotein (SCO4142, or PstS) has been identified to date inS. coelicolor. Combining biochemical and mass spectrometry-based approaches, we have isolated and characterized the membrane glycoproteome inS. coelicolor. A total of ninety-five high-confidence glycopeptides were identified which mapped to thirty-seven newS. coelicolorglycoproteins and a deeper understanding of glycosylation sites in PstS. Glycosylation sites were found to be modified with up to three hexose residues, consistent with what has been observed previously in otherActinobacteria.S. coelicolorglycoproteins have diverse roles and functions, including solute binding, polysaccharide hydrolases, ABC transporters, and cell wall biosynthesis, the latter being of potential relevance to the antibiotic-sensitive phenotype ofpmtmutants. Null mutants in genes encoding a putatived-Ala-d-Ala carboxypeptidase (SCO4847) and anl,d-transpeptidase (SCO4934) were hypersensitive to cell wall-targeting antibiotics. Additionally, thesco4847mutants displayed an increased susceptibility to lysozyme treatment. These findings strongly suggest that both glycoproteins are required for maintaining cell wall integrity and that glycosylation could be affecting enzyme function.IMPORTANCEIn prokaryotes, the role of protein glycosylation is poorly understood due to our limited understanding of their glycoproteomes. In someActinobacteria, defects in protein O-glycosylation have been shown to retard growth and result in hypersensitivity to cell wall-targeting antibiotics, suggesting that this modification is important for maintaining cell wall structure. Here, we have characterized the glycoproteome inStreptomyces coelicolorand shown that glycoproteins have diverse roles, including those related to solute binding, ABC transporters, and cell wall biosynthesis. We have generated mutants encoding two putative cell wall-active glycoproteins and shown them to be hypersensitive to cell wall-targeting antibiotics. These findings strongly suggest that both glycoproteins are required for maintaining cell wall integrity and that glycosylation affects enzyme function.

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