scholarly journals ENZYME ACTIVITIES DURING THE ASEXUAL CYCLE OF NEUROSPORA CRASSA

1968 ◽  
Vol 37 (1) ◽  
pp. 81-88 ◽  
Author(s):  
G. J. Stine
Keyword(s):  
Neurospora Crassa ◽  
Mycelial Growth ◽  
Germ Tube ◽  
Enzyme Synthesis ◽  
Nicotinamide Adenine ◽  
Glutamic Dehydrogenase ◽  
Specific Activities ◽  
Early Phases ◽  
Asexual Cycle ◽  
Logarithmic Growth

Three enzymes, (a) nicotinamide adenine diphosphate-dependent glutamic dehydrogenase (NAD enzyme), (b) nictoinamide adenine triphosphate-dependent glutamic dehydrogenase (NADP enzyme), and (c) nicotinamide-adenine dinucleotidase (NADase), were measured in separate extracts of Neurospora crassa grown in Vogel's medium N and medium N + glutamate. Specific activities and total units per culture of each enzyme were determined at nine separate intervals phased throughout the asexual cycle. The separate dehydrogenases were lowest in the conidia, increased slowly during germination, and increased rapidly during logarithmic mycelial growth. The amounts of these enzymes present during germination were small when compared with those found later during the production of the conidiophores. The NAD enzyme may be necessary for pregermination synthesis. The NADP-enzyme synthesis was associated with the appearance of the germ tube. Although higher levels of the dehydrogenases in the conidiophores resulted in more enzyme being found in the differentiated conidia, the rate of germination was uneffected. The greatest activity for the NADase enzyme was associated with the conidia, early phases of germination, and later production of new conidia. NADase decreased significantly with the onset of logarithmic growth, remained low during the differentiation of conidiophores, and increased considerably as the conidiophores aged.

ENZYME ACTIVITIES DURING THE ASEXUAL CYCLE OF NEUROSPORA CRASSA: I. SUCCINIC DEHYDROGENASE

1967 ◽  
Vol 13 (9) ◽  
pp. 1203-1210 ◽  
Author(s):  
G. J. Stine
Keyword(s):  
Neurospora Crassa ◽  
Enzyme Activities ◽  
Soluble Protein ◽  
Mycelial Growth ◽  
Germ Tube ◽  
Succinic Dehydrogenase ◽  
Growth Yield ◽  
Conidial Germination ◽  
Germination And Growth ◽  
Asexual Cycle

Separate extracts of Neuorospora crassa grown either in Vogel's medium N, medium N + glutamate, or medium N which had been made deficient in zinc, were assayed for succinic dehydrogenase and soluble protein at intervals throughout the asexual cycle. Succinic dehydrogenase, although apparently unnecessary for either the formation of conidia or conidial germination, does appear to be necessary for mycelial growth and for the production of conidiophores. Differences in the amount of enzyme during morphologically distinct states of differentiation (i.e. production of the germ tube and production of the conidiophore) may serve as an indicator of significant changes in the physiology of Neurospora at these times during development.The level of succinic dehydrogenase in the conidiophore before its differentiation into conidia appears to influence the amount of this enzyme found in the conidia. This is in keeping with the idea that conditions prevailing in the cytoplasm before the formation of conidia may directly influence the constituents subsequently found in the conidia which determine conidial viability, rate of germination, and growth yield.

Enzyme activities during the asexual cycle of Neurospora crassa. III. Nicotinamide adenosine diphosphate glycohydrolase

1969 ◽  
Vol 15 (11) ◽  
pp. 1249-1254 ◽  
Author(s):  
G. J. Stine
Keyword(s):  
Neurospora Crassa ◽  
Growth Medium ◽  
Mycelial Growth ◽  
Specific Activity ◽  
Adenosine Diphosphate ◽  
Water Soluble ◽  
Wild Type ◽  
Liquid Environment ◽  
Normal Differentiation ◽  
Asexual Cycle

The level and specific activity of nicotinamide adenosine diphosphate glycohydrolase (NADase) were followed throughout the asexual cycle in Neurospora crassa. A large quantity of NADase associated with the conidia was water soluble. NADase activity rapidly disappeared from the growth medium during conidial germination and from early logarithmic mycelial growth. As the mycelia aged, the enzyme accumulated in the growth medium and in the aging aconidial conidiophores, regardless of their inability to produce conidia. Since the enzyme was synthesized as the culture aged, it appears that the conidiophores age quickly with respect to their production of NADase. Conidia produced from conidiophores of the wild-type culture contained about the same quantity of NADase as the inoculum conidia. The accumulation of NADase in the conidia of wild-type Neurospora is due to the normal differentiation of these conidia in the absence of a liquid environment. The enzyme becomes locked into the conidia being differentiated from conidiophores that contain large amounts of the NADase activity.

scholarly journals Saprophytic microorganisms with potential for biological control of Botrytis cinerea on Geraldton waxflower flowers

2001 ◽  
Vol 41 (5) ◽  
pp. 697 ◽  
Author(s):  
D. R. Beasley ◽  
D. C. Joyce ◽  
L. M. Coates ◽  
A. H. Wearing
Keyword(s):  
Botrytis Cinerea ◽  
Mycelial Growth ◽  
Germ Tube ◽  
Conidial Germination ◽  
Pseudomonas Sp ◽  
Trichoderma Spp ◽  
Fusarium Sp ◽  
Flower Abscission ◽  
Germ Tube Elongation

Saprophytic bacteria, yeasts and filamentous fungi were isolated from Geraldton waxflower flowers and screened to identify potential antagonism towards Botrytis cinerea. Isolates from other sources (e.g. avocado) were also tested. Isolates were initially screened in vitro for inhibition of B. cinerea conidial germination, germ tube elongation and mycelial growth. The most antagonistic bacteria, yeasts and fungi were selected for further testing on detached waxflower flowers. Conidia of the pathogen were mixed with conidia or cells of the selected antagonists, co-inoculated onto waxflower flowers, and the flowers were sealed in glass jars and incubated at 20˚C. The number of days required for the pathogen to cause flower abscission was determined. The most antagonistic bacterial isolate, Pseudomonas sp. 677, significantly reduced conidial germination and retarded germ tube elongation of B. cinerea. None of the yeast or fungal isolates tested was found to significantly reduce conidial germination or retard germ tube elongation, but several significantly inhibited growth of B. cinerea. Fusarium sp., Epicoccum sp. and Trichoderma spp. were the most antagonistic of these isolates. Of the isolates tested on waxflower, Pseudomonas sp. 677 was highly antagonistic towards B. cinerea and delayed waxflower abscission by about 3 days. Trichoderma harzianum also significantly delayed flower abscission. However, as with most of the fungal antagonists used, inoculation of waxflower flowers with this isolate resulted in unsightly mycelial growth.

scholarly journals Mutation in neurospora crassa with leaf extract of citrus aurantifolia and their soluble protein content

1970 ◽  
Vol 19 (2) ◽  
pp. 151-155
Author(s):  
Apurba Lal Ray ◽  
Mahbuba Akhter Jahan ◽  
Tahsina Rahim
Keyword(s):  
Neurospora Crassa ◽  
Protein Content ◽  
Soluble Protein ◽  
Mycelial Growth ◽  
Leaf Extract ◽  
Mutagenic Effect ◽  
Wild Type ◽  
Soluble Protein Content ◽  
Citrus Aurantifolia ◽  
Morphological Mutants

Leaf extract of Citrus aurantifolia exhibited remarkable inhibitor effect on the radial mycelial growth of Neurospora crassa. The extract also showed mutagenic effect and atleast six morphological mutants of the fungus were detected including albino (al 243), vigorous (vg 117), fluffy (fl 220), colonial (cl 232), conidial band (con. band 171) and dirty (dir 83). The mutants were used for estimation of soluble protein in comparison with the wild type (Ema). The soluble protein content increased to some extent in case of the mutants con. band 171 (192.86 μg/ml), cl 232 (188.57 μg/ml) and vg 117 (186.43 μg/ml) as compared to the wild type (182.14 μg/ml). On the other hand, the soluble protein content was remarkably decreased in case of the mutant al 243 (94.28 μg/ml), which was about 50% less than the control. This indicates that the leaf extract not only effect colony morphology but possesses profound effect on growth and metabolism of the fungus. Key words: Neurospora crassa; Mutation; Leaf extract; Soluble protein DOI: http://dx.doi.org/10.3329/dujbs.v19i2.8958 DUJBS 2010; 19(2): 151-155

Catabolite-controlled regulation of glutamate dehydrogenases of Neurospora crassa

1970 ◽  
Vol 16 (1) ◽  
pp. 33-40 ◽  
Author(s):  
M. Kapoor ◽  
A. K. Grover
Keyword(s):  
Neurospora Crassa ◽  
Glutamate Dehydrogenase ◽  
Growth Medium ◽  
Nicotinamide Adenine Dinucleotide ◽  
Nicotinamide Adenine Dinucleotide Phosphate ◽  
Reciprocal Relationship ◽  
The Other ◽  
Nicotinamide Adenine ◽  
Specific Enzyme ◽  
Other Hand

The effect of the presence of catabolites in the growth medium on the synthesis of the two glutamate dehydrogenases of Neurospora crassa is reported. It has been demonstrated that the nicotinamide adenine dinucleotide (NAD) specific glutamate dehydrogenase is subject to repression by sucrose and glucose. Nicotinamide adenine dinucleotide phosphate (NADP) specific glutamate dehydrogenase, on the other hand, is induced by increasing concentrations of the catabolite. These data suggest that a reciprocal relationship exists between these two enzymes during synthesis in the presence of catabolites. Growth in higher concentrations of sucrose led to the formation of two isoenzymes of the NADP-specific enzyme; the second or the minor isozyme is not produced at very low catabolite concentrations. The catabolite effects produced by sucrose are overcome by glutamate, if the latter is incorporated into the growth medium. Glutamate represses both the isozymes of NADP-specific enzyme.

scholarly journals Antifungal Efficacy of Plant Oils Containing Thymol and Carvacrol in Controlling Botrytis cinerea, the Causal Agent of Grape (Vitis vinifera) GrayMould

2018 ◽  
Vol 16 (02) ◽  
pp. 15-24
Author(s):  
Zaker M ◽  
Zaker L
Keyword(s):  
Essential Oils ◽  
Botrytis Cinerea ◽  
Spore Germination ◽  
Mycelial Growth ◽  
Germ Tube ◽  
Plant Diseases ◽  
Plant Oils ◽  
Horticultural Products ◽  
Antifungal Efficacy ◽  
Germ Tube Elongation

The efficacy of a large number of plant extracts and essential oils in controlling plant diseases has been proven worldwide. Botrytis cinerea has attacked a wide host range causing severe loss in the field and at storage. In this study the antifungal efficacy of essential oils of three medicinal plants namely wild marjoram (Zataria multifolia), wild savory (perennial) (Satureja mutica) and savory (annual) (Satureja hortensis) possessing these compounds at three concentrations: 50, 100 and 200 ppm were evaluated in controlling the mycelial growth, spore germination and germ tube elongation of B. cinerea. All treatments except savory (annual) essential oil at 50 ppm showed significant differences with the control in inhibiting the mycelial growth as well as spore germination and germ tube elongation of B. cinerea (p=0.01). It was also noted that wild marjoram at 100 ppm and wild savory (perennial) essential oils at 200 ppm could completely (100%) inhibit the growth of the fungus. Essential oils from wild marjoram and wild savory had higher antifungal activity than annual savory. Their suitable formulations could be prepared and used as safe alternatives for controlling moulds of horticultural products during storage. The Agriculturists 2018; 16(2) 15-24

scholarly journals Cellular and extracellular siderophores of Aspergillus nidulans and Penicillium chrysogenum.

1981 ◽  
Vol 1 (2) ◽  
pp. 94-100 ◽  
Author(s):  
G Charlang ◽  
B Ng ◽  
N H Horowitz ◽  
R M Horowitz
Keyword(s):  
Biological Activity ◽  
Neurospora Crassa ◽  
Aspergillus Nidulans ◽  
Water Activity ◽  
Penicillium Chrysogenum ◽  
Mycelial Growth ◽  
Culture Medium ◽  
Highly Active ◽  
Assay Procedure ◽  
Generally True

Aspergillus nidulans and Penicillium chrysogenum produce specific cellular siderophores in addition to the well-known siderophores of the culture medium. Since this was found previously in Neurospora crassa, it is probably generally true for filamentous ascomycetes. The cellular siderophore of A. nidulans is ferricrocin; that of P. chrysogenum is ferrichrome. A. nidulans also contains triacetylfusigen, a siderophore without apparent biological activity. Conidia of both species lose siderophores at high salt concentrations and become siderophore dependent. This has also been found in N. crassa, where lowering of the water activity has been shown to be the causal factor. We used an assay procedure based on this dependency to reexamine the extracellular siderophores of these species. During rapid mycelial growth, both A. nidulans and P. chrysogenum produced two highly active, unidentified siderophores which were later replaced by a less active or inactive product--coprogen in the case of P. chrysogenum and triacetylfusigen in the case of A. nidulans. N. crassa secreted coprogen only. Fungal siderophore metabolism is varied and complex.

GLUTAMIC DEHYDROGENASE FROM UREDOSPORES OF PUCCINIA HELIANTHI SCHW.

1963 ◽  
Vol 9 (3) ◽  
pp. 345-351 ◽  
Author(s):  
J. E. Smith
Keyword(s):  
Nicotinamide Adenine Dinucleotide ◽  
Chelating Agents ◽  
Nicotinamide Adenine ◽  
Metal Chelating ◽  
Puccinia Helianthi ◽  
Glutamic Dehydrogenase ◽  
Sulphydryl Groups

Glutamic dehydrogenase was extracted from germinated uredospores of Puccinia helianthi and partially purified. The enzyme was specific for nicotinamide-adenine dinucleotide was inhibited by several metal-chelating agents and was shown to possess sulphydryl groups essential for activity.

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