NINHYDRIN-POSITIVE SUBSTANCE ANALYSIS OF LARVAL HEMOLYMPH OF THE EASTERN HEMLOCK LOOPER, LAMBDINA FISCELLARIA FISCELLARIA (LEPIDOPTERA: GEOMETRIDAE) AND GROWTH OF ENTOMOPHTHORA EGRESSA PROTOPLASTS

1977 ◽  
Vol 109 (3) ◽  
pp. 341-346 ◽  
Author(s):  
Gary B. Dunphy ◽  
Richard A. Nolan ◽  
Imre S. Otvos

AbstractA ninhydrin-positive substance analysis of fourth instar larval hemolymph of the eastern hemlock looper, Lambdina fiscellaria fiscellaria (Guenée), was conducted. Two separate larval populations were reared on a defined diet during the early stages and later on fresh, young balsam fir foliage. The results indicated the presence of at least 38 compounds. L-glutamine and(or) L-asparagine, L-histidine, and L-lysine occurred at high concentrations (> 5000 nM/ml). Ammonia, L-arginine, L-threonine, L-serine, L-glutamic acid, glycine, L-alanine, L-valine, L-isoleucine, L-leucine, L-tyrosine, and L-phenylalanine occurred at intermediate levels (1000–5000 nM/ml). The current report of the presence of L-1-methylhistidine and L-3-methylhistidine is the second report of any methylated derivative of histidine in insect hemolymph. The results of the analytical study were used to modify the composition of Grace’s insect tissue culture medium which had previously been found to support growth of protoplasts of the looper pathogen Entomophthora egressa MacLeod and Tyrrell. Fungal growth indicated a shorter generation time (4.7 h) on the medium modified to more closely approximate the looper hemolymph as compared with the generation time (6.2 h) on Grace’s medium.

1977 ◽  
Vol 55 (1) ◽  
pp. 107-113 ◽  
Author(s):  
Gary B. Dunphy ◽  
Richard A. Nolan

The regeneration patterns for protoplasts of Entomophthora egressa MacLeod and Tyrrell grown on modified Grace's insect tissue culture medium supplemented with fetal calf serum (a highly modified version of Grace's medium lacking serum and more closely approximating the hemolymph of the eastern hemlock looper), Müller-Kögler's coagulated egg yolk medium supplemented with Tristearin, and water agar are documented. Protoplasts on liquid and egg yolk media had varying degrees of common developmental patterns. On liquid media, development involving prophyphal spheres and fusion spheres predominated. Hyphae emerged from the prohyphal spheres; however, the fusion spheres did not develop further. On the coagulated egg yolk medium, the individual, non-chain, cells coalesced and developed into pleomorphs which later developed into osmotic shock-resistant postprotoplasts. A postprotoplast gave rise to a hypha which produced a terminal conidium. Later resting spores were detected. Water agar supported scant mycelial growth as compared with that on coagulated egg yolk but more than that on the liquid media. Solid substrates appeared to favor mycelial development. Regeneration could be avoided by the addition of fresh Grace's modified medium to either coagulated egg yolk plates or to cultures with Grace's modified medium. Obtaining protoplasts from hyphae and the reversion of these protoplasts to form hyphae appeared to be a fixed property of E. egressa.This report is believed to be the first for reversion of protoplasts initially produced by non-enzymic means.


1989 ◽  
Vol 35 (2) ◽  
pp. 304-308 ◽  
Author(s):  
Gary B. Dunphy ◽  
Richard A. Nolan

The protoplast stages of Entomophaga aulicae grew in a medium based on the amino acid and amine composition of the hemolymph of the eastern hemlock looper, Lambdina fiscellaria fiscellaria. The optimum temperature and pH ranges for spindle-shaped protoplast growth were 15 to 25 °C and 5.5 to 6.5, respectively. Spindle-shaped protoplast development progressed asynchronously through the formation of mesoprotoplasts, elliptical mesoprotoplasts, and rod-shaped and spherical hyphal bodies. The production of these stages was not influenced by either medium pH or osmolality. Conidia were formed on conidiophores arising from spherical hyphal bodies near the surface of the culture medium. Changes in amino acid and amine levels during growth were correlated with the stage of fungal development. The major amino acids utilized during development included L-glutamine, L-asparagine, L-proline, L-leucine, L-isoleucine, L-tyrosine, and the amine O-phosphoethanolamine.Key words: Entomophaga aulicae, Lambdina fiscellaria fiscellaria, protoplasts, hemolymph, ninhydrin-positive compounds.


1940 ◽  
Vol 72 (6) ◽  
pp. 729-745 ◽  
Author(s):  
Jonas E. Salk ◽  
G. I. Lavin ◽  
Thomas Francis

A study of the antigenic potency of influenza virus inactivated by ultraviolet radiation has been made. Virus so inactivated is still capable of functioning as an immunizing agent when given to mice by the intraperitoneal route. In high concentrations inactivated virus appears to be nearly as effective as active virus but when quantitative comparisons of the immunity induced by different dilutions are made, it is seen that a hundredfold loss in immunizing capacity occurs during inactivation. Virus in suspensions prepared from the lungs of infected mice is inactivated more rapidly than virus in tissue culture medium. A standard for the comparison of vaccines of epidemic influenza virus is proposed.


1984 ◽  
Vol 4 (11) ◽  
pp. 2449-2454 ◽  
Author(s):  
E R Kaufman

A new protocol for inducing mutations in mammalian cells in culture by exposure to the thymidine analog 5-bromodeoxyuridine (BrdUrd) was established. This protocol, called "DNA-dependent" mutagenesis, involved the incorporation of BrdUrd into DNA under nonmutagenic conditions and the subsequent replication of the 5-bromouracil (BrUra)-containing DNA under mutagenic conditions but with no BrdUrd present in the culture medium. The mutagenic conditions were induced by allowing BrUra-containing DNA to replicate in the presence of high concentrations of thymidine. This generated high intracellular levels of dTTP and dGTP, causing nucleotide pool imbalance. The mutagenesis induced by this protocol was found to correlate with the level of BrUra substituted for thymine in DNA.


2018 ◽  
Vol 7 (2) ◽  
pp. 84-91
Author(s):  
Adil Laaziz ◽  
Souad Qjidaa ◽  
Yousra El Hammoudi ◽  
Abdelouahed Hajjaji ◽  
Amina Bouseta

The aim of this study was to evaluate the effect of three fungicides azoxystrobin (Ortiva), hexaconazole (Hexa) and pyrimethanil (Pyrus) for their ability to inhibit the radial growth and ochratoxin A (OTA) production by five ochratoxigenic strains of Aspergillus carbonarius and A. niger previously iso-lated from Moroccan grapes. Our results showed that, the addition of the fungicides to the Czapek Yeast Autolysate agar culture medium reduced the growth of the ochratoxigenic strains. Pyrimethanil caused total inhibition of spore germination and growth of the five strains, for all dose tested. Where-as hexaconazole totally inhibited the growth of 4 strains and gave growth for the MUCL 49227 strain (2.67 mm/day) at sublethal concentration. The reduction in radial growth was less marked for azoxystrobin, with growth rate varying between 0 and 6.37 mm/day depending on the strain and the azoxystrobin concentration. Analysis of variance showed that the effect of single factors (fungicides, concentration and strain) and their interactions on growth and OTA production were highly significant (P=0.000).These findings suggest that the use of tested fungicides have to potential for reduction in production of OTA.


1977 ◽  
Vol 89 (1) ◽  
pp. 235-238 ◽  
Author(s):  
P. E. Russell ◽  
A. E. A. Mussa

SummaryTwo systemic fungicides, benomyl and thiabendazole, were more active than the non-systemic fungicide Drazoxolon in inhibiting fungal growth in vitro. A similar pattern was obtained in glasshouse trials with benomyl and thiabendazole giving adequate protection at low concentrations while Drazoxolon was ineffective unless applied at 50% the commercial product concentration. A field trial using thiabendazole, Drazoxolon and a mixture of benomyl and thiram confirmed the glasshouse results.Some phytotoxicity was noticed with high concentrations of both benomyl and thiabendazole, but satisfactory disease control was achieved using fungicide concentrations which did not induce phytotoxicity.


Author(s):  
Rini Yanti ◽  
Hermina Nurdiawati ◽  
Puji Wulandari ◽  
Yudi Pranoto ◽  
Muhammad Nur Cahyanto

Turmeric rhizomes are commonly used in the culinary, pharmaceutical, herbal medicine, and beverage industries. On the contrary, turmeric leaves are underutilized.  The aims of this study were to extract the essential oil from turmeric leaves, characterize the chemical composition of the oil, and determine its antifungal activities against aflatoxin-producing fungi. Steam distillation was used to extract the essential oil from turmeric leaves. The properties of the oil were identified using GC-MS. Antimicrobial activities against Aspergillus flavus and Aspergillus parasiticus were determined. Spores of the fungi were inoculated into potato dextrose agar plates supplemented with various quantities of turmeric leaves essential oil and incubated at 30°C for 7 days. The oil's primary constituents were α-phelandrene(46.70 %), followed by α-terpinolene (17.39 %), 1,8-cineole (8.78 %), benzene (4.24 %), and 2-β pinene (3.64 %). At low (<1%) concentrations, the oil delayed mycelia formation and at high concentrations it significantly inhibit fungal growth (at 1%) and completely inhibit colony formation (at 2%) Additionally, the result show that turmeric leaves oil can inhibited fungus growth at the lowest concentration (0.25 %) when compared to the control over a seven-day incubation period.


2021 ◽  
Vol 43 ◽  
pp. e51656
Author(s):  
Nara Priscila Barbosa Bravim ◽  
Anatércia Ferreira Alves ◽  
José Fábio França Orlanda ◽  
Patricia Barbosa Rodrigues Silva

The objective of the present study was to isolate fungi from agricultural soils and evaluate fungal growth in culture medium contaminated with atrazine, glyphosate and pendimethalin. Filamentous fungi were isolated from agricultural soils and cultured in a modified culture medium containing 0, 10, 20, 50, and 100 μg mL-1 atrazine, glyphosate and pendimethalin for 14 days at 28°C. The fungi that presented optimal and satisfactory growth were plated in Sabouraud culture medium with 4% dextrose and containing the herbicides at concentrations of 0, 10, 20, 50, and 100 μg mL-1 for seven days at 28°C. The mean mycelial growth values were submitted to analysis of variance and the Tukey test (p < 0.05%) for comparison and relative growth determination, and maximum inhibition rates were calculated. The isolated fungi Aspergillus fumigatus, Fusarium verticillioides and Penicillium citrinum were shown to be resistant to atrazine, glyphosate and pendimethalin. F. verticillioides showed higher mean mycelial growth in the culture media contaminated with atrazine and glyphosate than the other two fungi. In the culture medium contaminated with pendimethalin, F. verticillioides, and A. fumigatus presented the highest mean mycelial growth values.


2020 ◽  
Vol 36 (6) ◽  
Author(s):  
Itaruã Machri Colla ◽  
Olavo Bilac Quaresma de Oliveira Filho ◽  
Janyeli Dorini Silva de Freitas ◽  
Míria Benetati Delgado Bertéli ◽  
Giani Andrea Linde ◽  
...  

Lentinus crinitus is a medicinal basidiomycete, little studied regarding the basic cultivation conditions, which is used in bioremediation and consumed by native Indians from the Brazilian Amazon. Also, it produces a fungal secondary metabolite panepoxydone that has been described as an essential regulator of the inflammatory and immune response. This study aimed to evaluate basic conditions of temperature, pH, and nitrogen concentration and source in the cultivation of L. crinitus mycelial biomass. In order to evaluate fungal growth temperature, 2% malt extract agar (MEA) medium, pH 5.5, was utilized from 19 to 40 °C. For pH, MEA had pH adjusted from 2 to 11 and cultivated at 28 °C. Urea or soybean meal was added to MEA to obtain final concentration from 0.5 and 16 g/L of nitrogen, pH of 5.5, cultivated at 28 °C. The best temperature growth varies from 31 to 34 ºC and the optimal one is 32.7º C, and the best pH ranges from 4.5 to 6.5 and the optimal one is 6.1. Protein or non-protein nitrogen concentration is inversely proportional to the mycelial biomass growth. Nitrogen concentrations of 2.0 g/L soybean meal and urea inhibit mycelial biomass growth in 11% and 12%, respectively, but high concentrations of 16.0 g/L nitrogen inhibit the growth in 46% and 95%, respectively. The fungus is robust and grows under extreme conditions of temperature and pH, but smaller adaptation with increasing nitrogen concentrations in the cultivation medium, mainly non-protein nitrogen.


Sign in / Sign up

Export Citation Format

Share Document