EFFECT OF NUTRITION ON GROWTH AND CHLAMYDOSPORE FORMATION IN BROWN AND GRAY CULTURES OF THIELAVIOPSIS BASICOLA

1956 ◽  
Vol 34 (4) ◽  
pp. 459-472 ◽  
Author(s):  
R. H. Stover

Physiological differences between brown and gray wild type cultures of Thielaviopsis basicola were sought in order to develop selective media for use in mutational studies, and as a basis for pathogenicity and ecological studies. The gray wild type was more thiamine-deficient, yielded less mycelium, and grew more slowly than the brown on all media tested regardless of composition and thiamine content. In liquid media both types were more thiamine-deficient on sucrose than on glucose, but the reverse was true on agar media. The gray type was inhibited more than the brown by malachite and methyl green. A two-layered thiamine-deficient agar medium, and one containing dyes, was selective for the brown type. Gray and brown types grew better on thiamine-deficient water agar and soil extract agar than on thiamine-deficient agar media containing 20 gm/l. of sugar and 1 gm./l. of nitrogen compounds. On thiamine-deficient media, distortion and extrusion of the contents of endoconidia and hyphae were more common with the gray wild type than the brown.Endoconidia, but not chlamydospores, were formed in varying amounts on all thiamine-deficient media. The addition of thiamine resulted in the abundant production of chlamydospores and greatly increased growth. Chlamydospore production was also influenced by the source of nitrogen. Certain amino acids were more inhibitory to chlamydospore formation by the brown than gray type and vice versa. Asparagine, for example, blocked chlamydospore formation by the brown but not the gray type, even though growth and endoconidial production were abundant. Mutants capable of overcoming this blockage were readily produced in culture.


1959 ◽  
Vol 5 (5) ◽  
pp. 431-439 ◽  
Author(s):  
Norman James

Numbers of bacteria and of fungi in a saline soil were about one-fifth of numbers in a Red River clay soil. Bacterial counts on two soil-extract agar media, one prepared from the saline soil and the other from Red River soil, were the same, and the populations on the two were the same as shown by the replica plating technique. They were larger than counts on sodium albuminate agar or on asparagin–mannitol agar. Likewise, fungal counts on either soil-extract agar, with 0.02% dipotassmm phosphate, 0.1% glucose, and 0.1% peptone, were higher than counts on Waksman's acidified medium, or on Martin's medium, or on Smith and Dawson's medium. Interestingly, fungal counts on a medium with the same three chemicals as the soil-extract media but with the soil extract replaced by water were as high as those on the soil-extract media. Different levels of potassium phosphate were tested in each of the above media. In each medium for bacteria, and in each for fungi, counts varied inversely as the amount of potassium phosphate. The same held true when sodium phosphate was used instead of potassium phosphate in each medium.



Author(s):  
M. H. Wheeler ◽  
W. J. Tolmsoff ◽  
A. A. Bell ◽  
R. D. Stipanovic

Melanin formation in the fungus Thielaviopsis basicola was examined by light and electron-transmission microscopy with methods described previously in studies of Verticillium dahliae (1,2). A wild-type isolate and an albino mutant of T. basicola were grown on potato-carrot-dextrose-agar medium at 24°C prior to chemical treatment. The wild-type isolate was examined and compared with the albino mutant before and after treatment with each of the following compounds that have been proposed as melanin intermediates in various fungi (3): (+)-scytalone [3,4-dihydro-3,6,8-trihydroxy-l-(2H)- naphthalenone]; 1,8-dihydroxynaphthalene (DHN); L-3,4-dihydroxyphenylalanine (DOPA); and catechol.



Microbiology ◽  
2006 ◽  
Vol 152 (12) ◽  
pp. 3691-3700 ◽  
Author(s):  
Xi Chen ◽  
Carol A. Kumamoto

During infection, the opportunistic fungal pathogen Candida albicans grows invasively into the tissues of its host, forming filaments that penetrate the host tissue. To search for genes that are important for invasive filamentation, a screen for mutants that were defective in invasion of agar medium was conducted. A mutant carrying an insertion mutation in the locus of a gene, termed here DRG1, was identified. DRG1 encodes a highly conserved cytoplasmic G protein, with orthologues in the genomes of organisms from humans to yeast and archaea. C. albicans strains lacking Drg1p were defective in producing filaments that penetrated agar media, but produced filaments normally under other conditions, such as during liquid growth. When inoculated intravenously into mice, the drg1 null mutant caused delayed lethality accompanied by delayed invasive growth in the kidneys of the host, in comparison with those of the wild-type strain. These results implicate Drg1p in the control of invasive filamentation in the laboratory, and in the progression of invasive disease in the host.



2005 ◽  
Vol 99 (5) ◽  
pp. 485-492 ◽  
Author(s):  
Takefumi Hamaki ◽  
Motomasa Suzuki ◽  
Ryosuke Fudou ◽  
Yasuko Jojima ◽  
Takayuki Kajiura ◽  
...  


Author(s):  
M. H. Wheeler ◽  
W. J. Tolmsoff ◽  
A. A. Bell

(+)-Scytalone [3,4-dihydro-3,6,8-trihydroxy-l-(2Hj-naphthalenone] and 1,8-di- hydroxynaphthalene (DHN) have been proposed as intermediates of melanin synthesis in the fungi Verticillium dahliae (1, 2, 3, 4) and Thielaviopsis basicola (4, 5). Scytalone is enzymatically dehydrated by V. dahliae to 1,3,8-trihydroxynaphthalene which is then reduced to (-)-vermelone [(-)-3,4- dihydro-3,8-dihydroxy-1(2H)-naphthalenone]. Vermelone is subsequently dehydrated to DHN which is enzymatically polymerized to melanin.Melanin formation in Curvularia sp., Alternaria sp., and Drechslera soro- kiniana was examined by light and electron-transmission microscopy. Wild-type isolates of each fungus were compared with albino mutants before and after treatment with 1 mM scytalone or 0.1 mM DHN in 50 mM potassium phosphate buffer, pH 7.0. Both chemicals were converted to dark pigments in the walls of hyphae and conidia of the albino mutants. The darkened cells were similar in appearance to corresponding cells of the wild types under the light microscope.



1988 ◽  
Vol 55 (4) ◽  
pp. 579-583 ◽  
Author(s):  
Lucas Dominguez ◽  
José Francisco Fernández ◽  
Victor Briones ◽  
José Luis Blanco ◽  
Guillermo Suárez

SummaryDifferent selective agar media were compared for the recovery and isolation of five species ofListeriafrom raw milk and cheese. The selective media examined were Beerens medium, MacBride medium and that described by Dominguezet al.(1984) with 6 mg/1 acriflavine, listeria selective agar medium (LSAM), and LSAM with 12 mg/1 acriflavine (LSAM × 2A); a non-selective yeast glucose Lemco agar was included for comparison. When the difference between listeria and the natural microflora of raw milk and cheese was 102cfu/ml, listeria could be isolated by direct plating on all media tested. When it was lower than 103–104cfu/ml, listeria were isolated by direct plating only on LSAM and LSAM × 2A. When the difference was greater than 104cfu/ml, a previous enrichment was necessary to isolate them. LSAM and LSAM × 2A media performed better than the other media tested for isolating listeria by direct plating and improved their isolation from dairy products. This superior performance was evaluated by the ability of these media to support colony formation of different species ofListeriatested, the easy recognition of these colonies from those formed by other microorganisms and by their capacity to inhibit the natural microflora of these foods.



2000 ◽  
Vol 182 (5) ◽  
pp. 1304-1312 ◽  
Author(s):  
Angeles Zorreguieta ◽  
Christine Finnie ◽  
J. Allan Downie

ABSTRACT Rhizobium leguminosarum secretes two extracellular glycanases, PlyA and PlyB, that can degrade exopolysaccharide (EPS) and carboxymethyl cellulose (CMC), which is used as a model substrate of plant cell wall cellulose polymers. When grown on agar medium, CMC degradation occurred only directly below colonies of R. leguminosarum, suggesting that the enzymes remain attached to the bacteria. Unexpectedly, when a PlyA-PlyB-secreting colony was grown in close proximity to mutants unable to produce or secrete PlyA and PlyB, CMC degradation occurred below that part of the mutant colonies closest to the wild type. There was no CMC degradation in the region between the colonies. By growing PlyB-secreting colonies on a lawn of CMC-nondegrading mutants, we could observe a halo of CMC degradation around the colony. Using various mutant strains, we demonstrate that PlyB diffuses beyond the edge of the colony but does not degrade CMC unless it is in contact with the appropriate colony surface. PlyA appears to remain attached to the cells since no such diffusion of PlyA activity was observed. EPS defective mutants could secrete both PlyA and PlyB, but these enzymes were inactive unless they came into contact with an EPS+ strain, indicating that EPS is required for activation of PlyA and PlyB. However, we were unable to activate CMC degradation with a crude EPS fraction, indicating that activation of CMC degradation may require an intermediate in EPS biosynthesis. Transfer of PlyB to Agrobacterium tumefaciens enabled it to degrade CMC, but this was only observed if it was grown on a lawn ofR. leguminosarum. This indicates that the surface ofA. tumefaciens is inappropriate to activate CMC degradation by PlyB. Analysis of CMC degradation by other rhizobia suggests that activation of secreted glycanases by surface components may occur in other species.



1963 ◽  
Vol 9 (2) ◽  
pp. 187-197 ◽  
Author(s):  
E. C. S. Chan ◽  
H. Katznelson ◽  
J. W. Rouatt

These studies are concerned with the growth interrelationships of mixed cultures of five soil organisms in soil extract and root extracts of 2-, 4-, and 8-week-old oats, soybeans, and wheat. Population changes of Agrobacterium radiobacter, Arthrobacter citreus, Azotobacter chroococcum, Bacillus cereus, and a Pseudomonas sp. in pure and mixed culture were followed by plating on selective media. B. cereus and A. chroococcum grew poorly alone or in mixed culture in the extracts. In soil extract, A. citreus predominated over, or was nearly equal in number to, the Gram-negative forms (Pseudomonas and Agrobacterium). In root extracts, Pseudomonas sp. always predominated over A. citreus in mixed culture. A. radiobacter was inhibited in mature root extracts (8-week-old plants) although in pure culture it recovered after a period. An antagonistic effect of Pseudomonas sp. on A. chroococcum plated on nitrogen-free agar medium was found to be related to the kind of agar used.



Author(s):  
Владимир Ермаков ◽  
Vlyadimir Ermakov ◽  
Оксана Датченко ◽  
Oksana Datchenko ◽  
Юлия Курлыкова ◽  
...  

The purpose of the study is to improve the selective supplement for selective media with the purpose to produce enterobacteria. Tasks of the study are to identify the sensitivity of strains obtained of enterobacteria in regard to an-tibiotics; develop a new selective supplement with antibiotics to the nutrient medium Drigalski Lactose Agar. Media should have a content that in the best way possible ensures the growth and reproduction of microorganisms of cer-tain species or family. Intensive biotechnology development and Microbiology allows today to develop new nutrient media and modify the already existing content of media. The object of the study was a new selective additive with antibiotics to the nutrient medium Drigalski Lactose Agar. 253 isolates of bacteria produced from the intestinal mi-crobiotope of different animal species have been the Material for research. The study was conducted in the period from 2010 to 2017. Carbenicillin 30±2.3 from the group of carboxypenicillins and piperacillin 37±2.5 from the group of ureidopenicillins, kanamycin 24±1.5, amikacin 26±1.7 and gentamicin 25±0,8, cefepime 38±3.2 from the group of IV generation cephalosporins, tetracycline 28±1.6, doxycycline 34±2.3 and chloramphenicol 31±2.5, nalidixic acid 37±2.8, trimethoprim 35±3,4 demonstrated the greatest antimicrobial activity against all cultures of enterobac-teria that has been achieved. The high resistance of enterobacteria was shown to benzylpenicillin from the group of natural penicillins, to streptomycin, cephalotine from the group of cephalosporins of the first generation, to polymyx-in B, to ofloxacin (tarivid) and metronidazole. Antibacterial drugs effective against the accompanying gram-positive and gram-negative microflora were considered as the samples of the selective components. Vancomycin from the group of glycopeptides, linezolid from the group of oxazolidinones, and telithromycin from the group of ketolides were chosen. Antibiotics vancomycin and telithromycin in a dose of 0.008 g/dm3, linezolid 0.004 g/dm3 were cho-sen as the selective additive to Drigalski Lactose Agar medium.



1989 ◽  
Vol 52 (5) ◽  
pp. 360-362 ◽  
Author(s):  
ZHEKO KOUNEV

A new three-step procedure (TSP) for the recovery of Yersinia enterocolitica 0:3 from frozen meat, salted and dried meat products, raw dried meat products, and cooked perishable sausages, has been developed. The TSP is based mainly on enrichment in 0.15 M phosphate-buffered saline at 25°C. In the TSP, selected dilutions of samples are enriched for 1, 2, 3, 4, 24, and 48 h and then plated onto nonselective and selective agar media after or without alkali treatment. Additional enrichment was performed with half of the samples at 25°C for 24 h, and the rest at 4°C for up to 2 wk, followed by alkali treatment and plating on selective agar medium. Recovery of Y. enterocolitica was better using the TSP than the other method used for isolating the organism from meats.



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