ABSTRACT
En el presente estudio se determinó la producción de cuerpos fructíferos de cinco cepas nativas de Agrocybe cylindracea sobre tres sustratos y dos tratamientos térmicos, a través del porcentaje de eficiencia biológica y la medición del diámetro de los píleos. Se encontró que el mayor porcentaje de eficiencia biológica de las cepas en los sustratos evaluados fue 115.84 %, que correspondió al sustrato constituido por 29% paja de trigo más 1% de harina de soya pasteurizado y obtenido por la cepa 58.01, la cual también produjo las mayores eficiencias biológicas en todos los sustratos evaluados. Al confrontar el porcentaje de eficiencia biológica en los diferentes sustratos, todas las cepas presentaron valores altos en el sustrato compuesto por 28% de paja de trigo, 1% harina de soya y CaCO3. Con respecto al diámetro de los cuerpos fructíferos, las cepas 58.01, 59.01, 60.01 y 638.08 produjeron píleos menores de 2 cm, entre 2-4 cm y mayores a 4.0 cm en los diferentes sustratos y tratamientos, excepto la cepa 59.01 que en el sustrato formulado con 29% de paja de trigo y 1% de harina de soya, solo produjo cuerpos fructíferos con píleos menores a 2 cm y entre 2-4 cm. En el análisis proximal de los basidiomas de las cepas evaluadas se obtuvo un alto porcentaje de proteínas, fibra cruda y carbohidratos, así como bajo porcentaje de grasas. Se recomienda que en futuras investigaciones o transferencia de tecnología a comunidades o entidades interesadas en el cultivo de este hongo, utilizar paja de trigo suplementada con harina de soya y como regulador de pH CaCO3, ya que en dicho sustrato se obtuvieron los mayores porcentajes de eficiencia biológica para la producción de cuerpos fructíferos de A. cylindracea.
This study determined the production of fruiting bodies of five native strains of Agrocybe cylindracea over three different substrates and two heat treatments, by the biological efficiency percentage and the measurement of diameters of pileus. The major percentage of biological efficiency found from the strains in the evaluated substrates was 115.84%, and corresponded to the substrate formulated by 29% of wheat straw and 1% of pasteurized soy flour, and obtained from the strain 58.01, which also produced the major biological efficiencies in all of the evaluated substrates. When confronting the percentage of biological efficiency in the different substrates, all the strains presented high values in the substrate comprising 28% of wheat straw, 1% of soy flour and CaCO3. In relation to the diameter of the fruiting bodies, the strains 58.01, 59.01, 60.01 and 638.08 produced pileus less than 2 cm, between 2-4 cm and greater than 4 cm in the different substrates and treatments, excepting the strain 59.01 which in the substrate formulated with 29% of wheat straw and 1% of soy flour, only produced fruiting bodies with pileus less than 2 cm and between 2-4 cm. In the chemical proximate analysis of the fruiting bodies of the tested strains, a high percentage of proteins, crude fiber and carbohydrates was obtained, and also a low percentage of fats. For future research or when transferring the technology to communities interested in mushroom cultivation, the utilization of wheat straw supplemented with soy flour and as a regulator of pH CaCO3 is recommended, as in this substrate the highest percentages of biological efficiency for the production of fruiting bodies of A. cylindracea where obtained.
Subject(s)
Humans , Agaricales , Agrocybe/growth & development , Fruiting Bodies, Fungal , Whole Foods , Soy Foods , TriticumABSTRACT
Agrocybe cylandracea es un hongo que se consume en el municipio de Técpan Guatemala, Chimaltennago, San Juan Ostuncalco, Quetzaltenango y las aldeas Escuachil y Vista Hermosa de San Antonio Sacatepéquez, San Marcos. En la presente investigación se utilizaron cinco cepas guatemaltecas de A. cylindracea determinándose la morfología colonial y el crecimiento micelial en diferentes medios de cultivo y pH, para obtener la mejor condición en su cultivo a nivel de laboratorio como paso previo a la obtención de biomasa fúngica, producción de inóculo y cuerpos fructíferos. Se determinó que todas las colonias de las cepas evaluadas mostraron las características morfológicas reportadas en la literatura para A. cylandracea (con excepción de la cantidad de micelio aéreo el cual fue abundante) en todos los medios y pH estudiados...
Subject(s)
Agrocybe , Hydrogen-Ion Concentration , MyceliumABSTRACT
<p><b>OBJECTIVE</b>To optimize the techniques for extracting hypotensive active peptides from Agrocybe aegerita.</p><p><b>METHODS</b>The effects of the liquid/solid ratio, extraction time and temperature, pH value of the initial liquid on the extraction percentage (EP) of the hypotensive active peptides were investigated, and inhibition percentage (IP) of the extracts on angiotensin I-converting enzyme was determined.</p><p><b>RESULTS</b>Optimal extraction of the hypotensive active peptides from Agrocybe aegerita was achieved with the liquid/solid ratio of 40:1, extraction time of 3 h, extraction temperature at 30 degrees Celsius;, and pH=8 of the initial liquid. The EP of the hypotensive active peptides from Agrocybe aegerita could reach 87.7% with IP of the extracts on angiotensin I-converting enzyme of 54.0%.</p><p><b>CONCLUSION</b>This method is simple and efficient for extracting hypotensive active peptides from Agrocybe aegerita.</p>
Subject(s)
Agrocybe , Chemistry , Antihypertensive Agents , Pharmacology , Chromatography, High Pressure Liquid , Methods , Dietary Proteins , Pharmacology , Peptides , PharmacologyABSTRACT
This study evaluated the optimal vegetative growth conditions and molecular phylogenetic relationships of eleven strains of Agrocybe cylindracea collected from different ecological regions of Korea, China and Taiwan. The optimal temperature and pH for mycelial growth were observed at 25degrees C and 6. Potato dextrose agar and Hennerberg were the favorable media for vegetative growth, whereas glucose tryptone was unfavorable. Dextrin, maltose, and fructose were the most effective carbon sources. The most suitable nitrogen sources were arginine and glycine, whereas methionine, alanine, histidine, and urea were least effective for the mycelial propagation of A. cylindracea. The internal transcribed spacer (ITS) regions of rDNA were amplified using PCR. The sequence of ITS2 was more variable than that of ITS1, while the 5.8S sequences were identical. The reciprocal homologies of the ITS sequences ranged from 98 to 100%. The strains were also analyzed by random amplification of polymorphic DNA (RAPD) using 20 arbitrary primers. Fifteen primers efficiently amplified the genomic DNA. The average number of polymorphic bands observed per primer was 3.8. The numbers of amplified bands varied based on the primers and strains, with polymorphic fragments ranging from 0.1 to 2.9 kb. The results of RAPD analysis were similar to the ITS region sequences. The results revealed that RAPD and ITS techniques were well suited for detecting the genetic diversity of all A. cylindracea strains tested.
Subject(s)
Agar , Agrocybe , Alanine , Arginine , Carbon , China , DNA , DNA, Ribosomal , Fructose , Genetic Variation , Glucose , Glycine , Histidine , Hydrogen-Ion Concentration , Korea , Maltose , Methionine , Nitrogen , Polymerase Chain Reaction , Solanum tuberosum , Taiwan , UreaABSTRACT
Agrocybe aegerita is an important mushroom cultivated in Korea, with good feel and a peculiar fragrance. A. aegerita can be cultivated throughout the year using culture bottles but is more susceptible to contamination than other mushrooms. Twenty-two pathogens were isolated from the fruiting bodies and compost of A. aegerita, and seven isolates were isolated from Pleurotus ostreatus to compare with the A. aegerita isolates, collected from Gimje, Iksan, Gunsan of Chonbuk, and Chilgok of Gyeongbuk Province in 2009. These isolates were identified based on morphological and molecular characteristics. Of the 29 isolates, 26 were identified as Trichoderma spp. and the remaining three were Aspergillus spp., Mucor spp., and Penicillium spp. A phylogenetic analysis revealed that the 26 isolates of Trichoderma were divided into four taxa, namely T. harzianum, T. pleuroticola, T. longibrachiatum, and T. atroviride. Among the Trichoderma spp., 16 isolates (55.2%) were identified as T. harzianum, six as T. pleuroticola (20.7%), two as T. longibrachiatum, and the remaining two were T. atroviride.
Subject(s)
Agaricales , Agrocybe , Aspergillus , Fruit , Korea , Mucor , Penicillium , Pleurotus , Soil , TrichodermaABSTRACT
The process of biodegradation in lingo-cellulosic materials is critically relevant to biospheric carbon. The study of this natural process has largely involved laboratory investigations, focused primarily on the biodegradation and recycling of agricultural by-products, generally using basidiomycetes species. In order to collect super white rot fungi and evaluate its ability to degrade lingo-cellulosic material, 35 fungal strains, collected from forests, humus soil, livestock manure, and dead trees, were screened for enzyme activities and their potential to decolorize the commercially used Poly-R 478 dye. In the laccase enzymatic analysis chemical test, 33 white rot fungi and 2 brown rot fungi were identified. The degradation ability of polycyclic aromatic hydrocarbons (PAHs) according to the utilized environmental conditions was higher in the mushrooms grown in dead trees and fallen leaves than in the mushrooms grown in humus soil and livestock manure. Using Poly-R 478 dye to assess the PAH-degradation activity of the identified strains, four strains, including Agrocybe pediades, were selected. The activities of laccase, MnP, and Lip of the four strains with PAH-degrading ability were highest in Pleurotus incarnates. 87 fungal strains, collected from forests, humus soil, livestock manure, and dead trees, were screened for enzyme activities and their potential to decolorize the commercially used Poly-R 478 dye on solid media. Using Poly-R 478 dye to assess the PAHdegrading activity of the identified strains, it was determined that MKACC 51632 and 52492 strains evidenced superior activity in static and shaken liquid cultures. Subsequent screening on plates containing the polymeric dye poly R-478, the decolorization of which is correlated with lignin degradation, resulted in the selection of a strain of Coriolus versicolor, MKACC52492, for further study, primarily due to its rapid growth rate and profound ability to decolorize poly R-478 on solid media. Considering our findings using Poly-R 478 dye to evaluate the PAH-degrading activity of the identified strains, Coriolus versicolor, MKACC 52492 was selected as a favorable strain. Coriolus versicolor, which was collected from Mt. Yeogi in Suwon, was studied for the production of the lignin-modifying enzymes laccase, manganese-dependent peroxidase (MnP), and lignin peroxidase (LiP).
Subject(s)
Humans , Agaricales , Agrocybe , Anthraquinones , Basidiomycota , Carbon , Coloring Agents , Fungi , Laccase , Lignin , Lip , Livestock , Manure , Mass Screening , Peroxidase , Peroxidases , Pleurotus , Polycyclic Aromatic Hydrocarbons , Polymers , Recycling , Soil , Sprains and Strains , TreesABSTRACT
Cytoprotective ability of polysaccharides isolated from different edible mushrooms was investigated on the 7-ketocholesterol-induced damaged cell line. Polysaccharide extracts from six different edible mushrooms-Flammulina velutipes, Peurotus ostreatus, Lentinus edodes, Agrocybe aegerita, Agaricus blazei, and Cordyceps militaris- were prepared by hot water extraction and alcohol precipitation. Cytoprotective ability was evaluated by measuring the viable cells of the normal embryonic liver cell line (BNL CL. 2) in the presence of 7-ketocholesterol. At 80 microgram/mL of 7-ketocholesterol, cytotoxicity was very high with a loss of 98% of viable cells after 20 h of incubation. With the addition of 200 microgram/mL of each polysaccharide isolate to the cell line containing 80 microgram/mL of 7-ketocholesterol, polysaccharide isolates from both Flammulina velutipes and Peurotus ostreatus could significantly inhibit the 7-ketochoelsterol-induced cytotoxicity in the cells. But other polysaccharide isolates were not effective in inhibiting cell damage caused by the oxLDL-induced cytotoxicity.
Subject(s)
Animals , Mice , Agaricales , Agaricus , Agrocybe , Cell Line , Cordyceps , Flammulina , Liver , Polysaccharides , Shiitake Mushrooms , WaterABSTRACT
Agrocybe cylindracea, an edible mushroom belonging to Bolbitiaceae, Agaricales, is widely used as invaluable medicinal material in the oriental countries. This study was initiated to find the genes expressed during the fruiting body formation of A. cylindracea. The cDNAs expressed differentially during fruiting body morphogenesis of A. cylindracea were isolated through subtractive hybridization between vegetative mycelia and fruiting bodies. The cDNAs expressed in the fruiting body morphogenesis of A. cylindracea were cloned and twenty genes were identified. Eleven were homologous to genes of known functions, three were homologous to genes in other organism without any function known. Six were completely novel genes specific to A. cylindracea so far examined. Some genes with known functions were a pleurotolysin, a self-assembling poreforming cytolysins; Aa-Pri1 and Pir2p, specifically induced genes during fruiting initiation of other mushroom, Agrocybe aegerita; an amino acid permease; a cytochrome P450; a MADS-box gene; a peptidylprolyl isomerase; and a serine proteinase. For other clones, no clear function was annotated so far. We believe the first report of the differentially expressed genes in fruiting process of A. cylindracea will be great helps for further research.