scholarly journals Functional Analysis of an Essential GSP1/Ran Ortholog Gene, CpRan1, from the Chestnut Blight Fungus Cryphonectria parasitica Using a Heterokaryon

2021 ◽  
Vol 7 (5) ◽  
pp. 332
Author(s):  
Dae-Hyuk Kim ◽  
Yo-Han Ko ◽  
Jeesun Chun
Keyword(s):  
Amino Acids ◽  
Functional Analysis ◽  
Mutant Allele ◽  
Microscopic Analysis ◽  
Essential Amino Acids ◽  
Cryphonectria Parasitica ◽  
Complementation Analysis ◽  
Null Mutant ◽  
Wild Type ◽  
Chestnut Blight Fungus

Functional analysis of a GSP1/Ran ortholog, CpRan1, from Cryphonectria parasitica was conducted. Genotype analysis revealed that the putative CpRan1-null mutant was a heterokaryotic transformant harboring two different types of nuclei, one with the wild-type CpRan1 allele and the other with the CpRan1-null mutant allele. The mycelial growth and colony morphology of the heterokaryotic transformant was normal. Microscopic analysis of the resulting conidia (aseptate and monokaryotic asexual spores) demonstrated that although normal germinating spores were observed from conidia harboring a nucleus with the wild-type CpRan1 allele, a number of residual conidia that did not germinate existed. Complementation analysis using protoplasts from the heterokaryon with the wild-type CpRan1 allele confirmed that the CpRan1 gene is essential to C. parasitica. Complementation analysis using the various CpRan1 chimera constructs allowed us to perform a functional analysis of essential amino acids of the CpRan1. Among the four suggested essential amino acids, Lys-97 for ubiquitination was determined to not be an essential residue. Moreover, the CpRan1-null mutant allele was successfully complemented with mouse Ran gene, which suggested that the biological function of Ran gene is evolutionary conserved and that our heterokaryon rescue can be applied for the functional analysis of heterologous genes.

scholarly journals Characterization of a Hypovirus-Regulated Septin Cdc11 Ortholog, CpSep1, from the Chestnut Blight Fungus Cryphonectria parasitica

2019 ◽  
Vol 32 (3) ◽  
pp. 286-295 ◽  
Author(s):  
Myeongjin Jo ◽  
Kum-Kang So ◽  
Yo-Han Ko ◽  
Jeesun Chun ◽  
Jung-Mi Kim ◽  
...  
Keyword(s):  
Cryphonectria Parasitica ◽  
Chestnut Blight ◽  
Null Mutant ◽  
Wild Type ◽  
Chestnut Blight Fungus ◽  
Germination Process ◽  
Cryphonectria Hypovirus ◽  
Null Mutants

We identified a protein spot showing downregulation in the presence of Cryphonectria hypovirus 1 and tannic acid supplementation as a septin subunit with the highest homology to the Aspergillus nidulans aspA gene, an ortholog of the Saccharomyces cerevisiae Cdc11 gene. To analyze the functional role of this septin component (CpSep1), we constructed its null mutant and obtained a total of eight CpSep1-null mutants from 137 transformants. All CpSep1-null mutants showed retarded growth, with fewer aerial mycelia and intense pigmentation on plates of potato dextrose agar supplemented with L-methionine and biotin. When the marginal hyphae were examined, hyperbranching was observed in contrast to the wild type. The inhibition of colonial growth was partially recovered when the CpSep1-null mutants were cultured in the presence of the osmostabilizing sorbitol. Conidia production of the CpSep1-null mutants was significantly increased by at least 10-fold more. Interestingly, the conidial morphology of the CpSep1-null mutants changed to circular in contrast to the typical rod-shaped spores of the wild type, indicating a role of septin in the spore morphology of Cryphonectria parasitica. However, no differences in the germination process were observed. Virulence assays using excised chestnut bark, stromal pustule formation on chestnut stems, and apple inoculation indicated that the CpSep1 gene is important in pathogenicity.

Untersuchungen über den Kaliumtransport in E. coli B

1971 ◽  
Vol 26 (9) ◽  
pp. 887-893 ◽  
Author(s):  
U. Zimmermann ◽  
G. Pilwat
Keyword(s):  
Amino Acids ◽  
Incubation Medium ◽  
Potassium Level ◽  
Potassium Concentration ◽  
Essential Amino Acids ◽  
Type B ◽  
Wild Type ◽  
E Coli ◽  
Stabilization Effect ◽  
Intracellular Potassium Concentration

An intracellular concentration of potassium in E. coli B 525 stationary for several hours is only attained by addition of the essential amino acids histidine and leucine, or ammonium chloride, to the incubation medium. The level of the stationary intracellular potassium concentration is dependent upon the concentration of these substances.The two other combinations of the essential amino acids (leucine/methionine and histidine/methionine) and the single amino acids show no stabilization effect upon the internal stationary potassium level.In the case of the wild type B 163, the instability of the stationary internal potassium concentration, and the corresponding effect of the above mentioned substances, is not so significant. Therefore the instability which is observed in the case of B 525 can be deduced from the mutation.

scholarly journals A Host Factor Involved in Hypovirus Symptom Expression in the Chestnut Blight Fungus, Cryphonectria parasitica

2007 ◽  
Vol 82 (2) ◽  
pp. 740-754 ◽  
Author(s):  
M. Iqbal Faruk ◽  
Ana Eusebio-Cope ◽  
Nobuhiro Suzuki
Keyword(s):  
Insertion Site ◽  
Cryphonectria Parasitica ◽  
Inverse Pcr ◽  
Chestnut Blight ◽  
Wild Type ◽  
Targeted Disruption ◽  
Chestnut Blight Fungus ◽  
Virulence Attenuation ◽  
Symptom Modulation ◽  
Sequence Similarities

ABSTRACT The prototype hypovirus CHV1-EP713 causes virulence attenuation and severe suppression of asexual sporulation and pigmentation in its host, the chestnut blight fungus, Cryphonectria parasitica. We identified a factor associated with symptom induction in C. parasitica using a transformation of C. parasitica strain EP155 with a full-length cDNA clone from a mild mutant virus strain, Cys(72). This was accomplished by using mutagenesis of the transformant fungal strain TCys(72)-1 by random integration of plasmid pHygR, conferring hygromycin resistance. The mutant, namA (after nami-gata, meaning wave shaped), showed an irregular fungal morphology with reduced conidiation and pigmentation while retaining similar levels of virulence and virus accumulation relative to TCys(72)-1- or Cys(72)-infected strain EP155. However, the colony morphology of virus-cured namA (VC-namA) was indistinguishable from those of EP155 and virus-cured TCys(72)-1 [VC-TCys(72)-1]. The phenotypic difference between VC-namA and VC-TCys(72)-1 was found only when these strains infected with the wild type or certain mutant CHV1-EP713 strains but not when infected with Mycoreovirus 1. Sequence analysis of inverse-PCR-amplified genomic DNA fragments and cDNA identified the insertion site of the mutagenic plasmid in exon 8 of the nam-1 gene. NAM-1, comprising 1,257 amino acids, shows sequence similarities to counterparts from other filamentous fungi and possesses the CorA domain that is conserved in a class of Mg2+ transporters from prokaryotes and eukaryotes. Complementation assays using the wild-type and mutant alleles and targeted disruption of nam-1 showed that nam-1 with an extension of the pHygR-derived sequence contributed to the altered phenotype in the namA mutant. The molecular mechanism underlying virus-specific fungal symptom modulation in VC-namA is discussed.

Accumulation of casein-derived peptides during growth of proteinase-positive strains of Lactococcus lactis in milk: their contribution to subsequent bacterial growth is impaired by their internal transport

2000 ◽  
Vol 67 (2) ◽  
pp. 233-240 ◽  
Author(s):  
CATHERINE FOUCAUD ◽  
VINCENT JUILLARD
Keyword(s):  
Amino Acids ◽  
Lactococcus Lactis ◽  
Nutritional Value ◽  
Essential Amino Acids ◽  
Peptide Transport ◽  
Wild Type ◽  
Transport Mutants ◽  
Time Courses ◽  
Internal Transport ◽  
Type Strains

To explain the limited nutritional value of milk cultured with proteinase-positive (Prt+) strains of Lactococcus lactis for the subsequent growth of dairy lactococci, we investigated further the time courses of modifications in the free amino acid and peptide contents of cultured milk. When growing in milk for up to 24 h, Prt+ strains of Lc. lactis progressively accumulated amino acids and casein-derived peptides. The growth of proteinase-negative (Prt−) wild-type strains and peptide transport mutants of Lc. lactis in cultured milk showed that casein-derived peptides could sustain growth up to 5×108 cfu/ml, depending on the extent of casein degradation during the preliminary growth of Prt+ strains and the Prt− strains. Of the casein-derived oligopeptides, <25% were transported into the cell and used for Lc. lactis growth. However, they played a prominent role, contributing 90% to growth. In contrast, di- and tripeptides did not contribute to growth, suggesting that either few were released from caseins or they did not supply essential amino acids.

scholarly journals Role of Cystathionine β-Lyase in Catabolism of Amino Acids to Sulfur Volatiles by Genetic Variants of Lactobacillus helveticus CNRZ 32

2007 ◽  
Vol 73 (9) ◽  
pp. 3034-3039 ◽  
Author(s):  
Won-Jae Lee ◽  
Dattatreya S. Banavara ◽  
Joanne E. Hughes ◽  
Jason K. Christiansen ◽  
James L. Steele ◽  
...  
Keyword(s):  
Amino Acids ◽  
Genetic Variants ◽  
Solid Phase ◽  
Dimethyl Disulfide ◽  
Lactobacillus Helveticus ◽  
Gas Chromatography Mass Spectrometry ◽  
Null Mutant ◽  
Wild Type ◽  
Sulfur Containing

ABSTRACT Catabolism of sulfur-containing amino acids plays an important role in the development of cheese flavor. During ripening, cystathionine β-lyase (CBL) is believed to contribute to the formation of volatile sulfur compounds (VSCs) such as methanethiol and dimethyl disulfide. However, the role of CBL in the generation of VSCs from the catabolism of specific sulfur-containing amino acids is not well characterized. The objective of this study was to investigate the role of CBL in VSC formation by Lactobacillus helveticus CNRZ 32 using genetic variants of L. helveticus CNRZ 32 including the CBL-null mutant, complementation of the CBL-null mutant, and the CBL overexpression mutant. The formation of VSCs from methionine, cystathionine, and cysteine was determined in a model system using gas chromatography-mass spectrometry with solid-phase microextraction. With methionine as a substrate, CBL overexpression resulted in higher VSC production than that of wild-type L. helveticus CNRZ 32 or the CBL-null mutant. However, there were no differences in VSC production between the wild type and the CBL-null mutant. With cystathionine, methanethiol production was detected from the CBL overexpression variant and complementation of the CBL-null mutant, implying that CBL may be involved in the conversion of cystathionine to methanethiol. With cysteine, no differences in VSC formation were observed between the wild type and genetic variants, indicating that CBL does not contribute to the conversion of cysteine.

Characterization of the ERK homologue CpMK2 from the chestnut blight fungus Cryphonectria parasitica

Microbiology ◽  
2005 ◽  
Vol 151 (5) ◽  
pp. 1349-1358 ◽  
Author(s):  
Eun-Sil Choi ◽  
Hea-Jong Chung ◽  
Myoung-Ju Kim ◽  
Seung-Moon Park ◽  
Byeong-Jin Cha ◽  
...  
Keyword(s):  
Growth Conditions ◽  
Cryphonectria Parasitica ◽  
Mitogen Activated Protein Kinase ◽  
Wild Type ◽  
Growth Defects ◽  
Chestnut Blight Fungus ◽  
Phosphorylation Level ◽  
Solid Media ◽  
Mitogen Activated Protein ◽  
Hypovirulent Strain

The Cryphonectria parasitica gene cpmk2, which encodes a mitogen-activated protein kinase belonging to the yeast extracellular signalling-regulated kinase (YERK1) subfamily, was isolated and its biological function was examined. Disruption of cpmk2 resulted in impaired pigmentation and abolished conidiation. Growth defects were observed in the cpmk2 mutant grown on solid plates, but growth of the mutant appeared normal in liquid media, including EP complete and PD broth, suggesting that the cpmk2 gene is involved in sensing and responding to growth conditions. The mutant's production of laccase, as measured by the size of the coloured area produced on tannic-acid-supplemented plates, was significantly reduced compared with the wild-type, but the intensity of the coloured area was unchanged, suggesting that the reduced laccase activity was owing to reduced growth on solid media rather than transcriptional downregulation. A dramatic reduction observed in the canker area produced by the cpmk2 mutant compared with the wild-type, even more severe than that of a hypovirulent strain, can also be ascribed to defective growth on solid surfaces rather than to impairments in a virulence factor(s). Downregulation of the pheromone gene Mf2/1 was also observed in the mutant, indicating a possible explanation for the regulation of the pheromone precursor gene in filamentous fungi and suggesting the presence of the yeast-like pheromone-responsive pathway in C. parasitica. Immunoblot analyses revealed that the phosphorylation level of CpMK2 increased in both virus-free and virus-containing strains in liquid cultures of up to 5 days old and decreased in older cultures. Moreover, the CpMK2 phosphorylation level increased in both strains after transfer from liquid to solid medium. However, levels of phosphorylated CpMK2 were similar in the two strains, suggesting that CpMK2, unlike CpMK1, is not under the direct control of a hypovirus.

scholarly journals Hypovirulence-associated traits induced by a mycovirus of Cryphonectria parasitica are mimicked by targeted inactivation of a host gene.

1993 ◽  
Vol 13 (12) ◽  
pp. 7782-7792 ◽  
Author(s):  
L Zhang ◽  
A C Churchill ◽  
P Kazmierczak ◽  
D H Kim ◽  
N K Van Alfen
Keyword(s):  
Type Strain ◽  
Wild Type Strain ◽  
Cryphonectria Parasitica ◽  
Apple Fruit ◽  
Host Gene ◽  
Fruiting Bodies ◽  
Null Mutant ◽  
Wild Type ◽  
Fungal Virulence ◽  
Double Stranded Rna

Expression of the Vir2 gene of Cryphonectria parasitica is down-regulated in strains of the fungus containing a double-stranded RNA genetic element that reduces fungal virulence (W. A. Powell and N. K. Van Alfen, Mol. Cell. Biol. 7:3688-3693, 1987). We have sequenced the Vir2 gene and characterized its structure; the mRNA contains a short open reading frame whose product has structural similarities to several fungal pheromones. A null mutant was constructed by homologous recombination to determine the function of the Vir2 gene and whether its disruption resulted in any of the altered phenotypes exhibited by many hypovirulent strains, such as reductions in virulence, pigmentation, and sporulation. The Vir2 null mutant (18dm) exhibited a wild-type phenotype with respect to gross colony morphology, growth rate, pigmentation, asexual spore viability, and virulence in apple fruit and chestnut trees. However, numbers of asexual fruiting bodies (pycnidia) and conidia were reduced significantly in comparison with the wild-type strain EP155/2. In sexual crosses of 18dm with a wild-type strain of the opposite mating type, perithecia (sexual fruiting bodies) developed but were barren. Deletion of the Vir2 gene results in a phenotype that mimics that of many double-stranded-RNA-containing hypovirulent strains; i.e., the null mutant exhibits significant reductions in asexual sporulation and pycinidum production as well as impaired sexual crossing ability. To our knowledge, this is the first report of the partial reproduction of a virus-induced phenotype by deletion of a virus-perturbed host gene.

scholarly journals Communicating the nutritional value of sugar in Drosophila

2018 ◽  
Vol 115 (12) ◽  
pp. E2829-E2838 ◽  
Author(s):  
Farhan Abu ◽  
Justin G. Wang ◽  
Yangkyun Oh ◽  
Jingjing Deng ◽  
Thomas A. Neubert ◽  
...  
Keyword(s):  
Amino Acids ◽  
Fatty Acids ◽  
Real Time ◽  
Olfactory System ◽  
Nutritional Value ◽  
Essential Amino Acids ◽  
Wild Type ◽  
Correlation Analyses

Sweet-insensitive Drosophila mutants are unable to readily identify sugar. In presence of wild-type (WT) flies, however, these mutant flies demonstrated a marked increase in their preference for nutritive sugar. Real-time recordings of starved WT flies revealed that these flies discharge a drop from their gut end after consuming nutritive sugars, but not nonnutritive sugars. We proposed that the drop may contain a molecule(s) named calorie-induced secreted factor (CIF), which serves as a signal to inform other flies about its nutritional value. Consistent with this, we observed a robust preference of flies for nutritive sugar containing CIF over nutritive sugar without CIF. Feeding appears to be a prerequisite for the release of CIF, given that fed flies did not produce it. Additionally, correlation analyses and pharmacological approaches suggest that the nutritional value, rather than the taste, of the consumed sugar correlates strongly with the amount (or intensity) of the released CIF. We observed that the release of this attractant signal requires the consumption of macronutrients, specifically nutritive sugars and l-enantiomer essential amino acids (l-eAAs), but it is negligibly released when flies are fed nonnutritive sugars, unnatural d-enantiomer essential amino acids (d-eAAs), fatty acids, alcohol, or salts. Finally, CIF (i) is not detected by the olfactory system, (ii) is not influenced by the sex of the fly, and (iii) is not limited to one species of Drosophila.

scholarly journals A Mutant of the Bck1 Homolog from Cryphonectria parasitica Resulted in Sectorization with an Impaired Pathogenicity

2016 ◽  
Vol 29 (4) ◽  
pp. 268-276 ◽  
Author(s):  
Jung-Mi Kim ◽  
Joong-Gi Lee ◽  
Suk-Hyun Yun ◽  
Kum-Kang So ◽  
Yo-Han Ko ◽  
...  
Keyword(s):  
Cell Wall ◽  
Signal Transduction Pathway ◽  
Cryphonectria Parasitica ◽  
Cell Wall Integrity ◽  
Mitogen Activated Protein Kinase ◽  
Null Mutant ◽  
Genetic Changes ◽  
Chestnut Blight Fungus ◽  
Mitogen Activated Protein ◽  
Protein Kinase Kinase

CpBck1, an ortholog of the cell-wall integrity mitogen-activated protein kinase kinase kinase of Saccharomyces cerevisiae, was cloned and characterized from the chestnut blight fungus Cryphonectria parasitica. The CpBck1-null mutant displayed cell wall integrity–related phenotypic changes such as abnormal cell morphology and wall formation and hypersensitivity to cell wall-disrupting agents. In addition, the mutant showed severely retarded growth without any sign of normal development, such as hyphal differentiation, conidiation, or pigmentation. As the culture proceeded, the mutant colony showed sporadic sectorization. Once sectored, the sectored phenotype of robust mycelial growth without differentiation was stably inherited. Compared with the wild type, both the parental CpBck1-null mutant and the sectored progeny exhibited marked impaired virulence. The present study revealed that a mutation in a signaling pathway component related to cell-wall integrity resulted in sporadic sectorization and these sectored phenotypes were stably inherited, suggesting that this signal transduction pathway is implicated in adaptive genetic changes for sectorization.

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