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1.
Article | IMSEAR | ID: sea-220478

RÉSUMÉ

Quality spawns are an important factor to support the success of button mushroom cultivation. The quality of mushroom spawn is in?uenced by the nutritional composition of the media. The purpose of this study was to determine the best media for the growth of F0 and F1 button mushroom. The research was carried out in March-May 2021 at the Biology Laboratory, Faculty of Agroindustry, University of Mercu Buana Yogyakarta. The study consisted of 2 series of experiments. This study consisted of 2 series of experiments. The ?rst experiment was to test the growth quality of F0 champignon on 3 types media, that is potato dextrose agar (PDA),mung been sprout extract media, and white sweet potato media. The second experiment tested the growth quality of F1 button mushroom grown on three types of media, that is corn, barley and sorghum. Both experiment were single factor trials arranged in a completely randomized design (CRD) with three replications, and each replication consisted of 5 units. The results showed that the growth of F0 button mushroom grown on PDA media and mung bean sprout extract was better than white sweet potato extract media. For the growth of F1 button mushroom, the best media was corn, the second was sorghum and the third was barley

2.
Mycobiology ; : 421-428, 2018.
Article de Anglais | WPRIM | ID: wpr-729733

RÉSUMÉ

The white button mushroom (Agaricus bisporus) is one of the most widely cultivated species of edible mushroom. Despite its economic importance, relatively little is known about the genetic diversity of this species. Illumina paired-end sequencing produced 43,871,558 clean reads and 69,174 contigs were generated from five offspring. These contigs were subsequently assembled into 57,594 unigenes. The unigenes were annotated with reference genome in which 6,559 unigenes were associated with clusters, indicating orthologous genes. Gene ontology classification assigned many unigenes. Based on genome data of the five offspring, 44 polymorphic simple sequence repeat (SSR) markers were developed. The major allele frequency ranged from 0.42 to 0.92. The number of genotypes and the number of alleles ranged from 1 to 4, and from 2 to 4, respectively. The observed heterozygosity and the expected heterozygosity ranged from 0.00 to 1.00, and from 0.15 to 0.64, respectively. The polymorphic information content value ranged from 0.14 to 0.57. The genetic distances and UPGMA clustering discriminated offspring strains. The SSR markers developed in this study can be applied in polymorphism analyses of button mushroom and for cultivar discrimination.


Sujet(s)
Agaricales , Allèles , Classification , 4252 , Oestrone , Fréquence d'allèle , Gene Ontology , Variation génétique , Génome , Génotype , Répétitions microsatellites
3.
Ciênc. rural ; Ciênc. rural (Online);44(2): 241-246, fev. 2014.
Article de Portugais | LILACS | ID: lil-701348

RÉSUMÉ

O cogumelo Agaricus bisporus é um cogumelo de clima temperado que requer baixa temperatura para a indução da frutificação. Essa exigência limita o seu cultivo no Brasil nos meses mais frios do ano ou exige a utilização de ambiente controlado, onerando muito a produção. Por isso, este trabalho teve como objetivo avaliar a produtividade de diferentes linhagens em função da temperatura de cultivo após a indução da frutificação. Diferentes linhagens de A. bisporus foram avaliadas quanto ao efeito da temperatura sobre a colonização do composto e a produtividade do cogumelo. As temperaturas de 21 e 25°C foram utilizadas durante a colonização do composto e, após a indução da frutificação, durante o ciclo de cultivo. Para todas as linhagens testadas, a temperatura de 25°C proporcionou maior velocidade de colonização do composto, favorecendo ciclos de cultivo mais curtos. Além disso, após a indução da frutificação a 18°C, a manutenção do ambiente de cultivo a 25°C proporcionou maior produtividade, quando comparada ao cultivo a 21°C. Para a linhagem mais produtiva, os três primeiros fluxos foram responsáveis por mais de 50% da produção total. Portanto, para um cultivo comercial em que é necessário manter volumes constantes de produção, os ciclos de cultivo poderiam ser limitados a três fluxos de produção.


The Agaricus bisporus is a button mushroom that requires low temperature to induce fruiting. This requirement limits our cultivation in Brazil during the coldest months of the year and requires the use of controlled environment. Therefore, this study aimed to assess the productivity of different strains depending on the growth temperature after induction of fruiting. A. bisporus strains were evaluated for the effect of temperature on the colonization of compost and mushroom productivity. Temperatures of 21 and 25°C were used for the substrate colonization and after induction of fruiting crop cycle. For all strains tested, temperature 25°C gave a quickly colonization of the compound, favoring shorter production cycles. Furthermore, after induction of fruiting at 18°C, maintaining the culture environment at 25°C gave a higher productivity to contrast with culture at 21°C. For the most productive strain, the first three streams were responsible for over 50% of total production. Thus, for a cash crop where it is necessary to maintain constant volumes of production, crop cycles could be limited to three productions flows.

4.
Braz. j. microbiol ; Braz. j. microbiol;43(3): 1137-1146, July-Sept. 2012. ilus, tab
Article de Anglais | LILACS | ID: lil-656684

RÉSUMÉ

Twenty seven bacterial isolates were isolated from superficial brown discolorations on the caps of cultivated Agaricus bisporus. After White Line Assay (WLA) and the assist of Biolog computer-identification system, isolates were divided into groups: (I) comprised ninteen bacterial isolates that positively responded to a Pseudomonas "reactans" reference strain (NCPPB1311) in WLA and were identified as Pseudomonas tolaasii, (II) comprised two isolates which were WLA+ towards the reference strain (JCM21583) of P. tolaasii and were proposed to be P. "reactans". The third group comprised six isolates, two of which weakly responded to the strain of P. tolaasii and were identified as P. gingeri whereas the other four were WLA- and identified as P. fluorescens (three isolates) and P. marginalis (one isolate). Isolates of P. tolaasii showed high aggressiveness compared with those of P. "reactans" in pathogenicity tests. Cubes of 1 cm³ of A. bisporus turned brown and decreased in size when were inoculated with 10 µl of P. tolaasii suspension containing 10(8) CFU ml-1, whereas a similar concentration of P. "reactans" caused only light browning. Fifty µl of the same concentration of P. tolaasii isolates gave typical brown blotch symptoms on fresh mushroom sporophores whereas the two P. "reactans" isolates caused superficial light discoloration only after inoculation with 100 µl of the same concentration. Mixture from both bacterial suspensions increased the brown areas formed on the pileus. This is the first pathogenicity report of P. tolasii and P. "reactans" isolated from cultivated A. bisporus in Egypt.


Sujet(s)
Humains , Agaricales/isolement et purification , Agaricus/isolement et purification , Antibactériens/isolement et purification , Pseudomonas fluorescens/isolement et purification , Échantillons Alimentaires , Méthodes , Virulence
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