scholarly journals Cultivation of Paecilomyces tenuipes using Mini-kit, small culture container

2012 ◽  
Vol 50 (2) ◽  
pp. 116-121 ◽  
Author(s):  
Sung-Hee Nam ◽  
Kwang Gill Lee ◽  
Joo Hong Yeo ◽  
Heui Sam Lee ◽  
Jae Sam Hwang ◽  
...  
Keyword(s):  
1975 ◽  
Vol 191 (1104) ◽  
pp. 387-411 ◽  

The responses of two characters, number of sternopleural chaetae and total yield of offspring (which depends on the mother’s genotype), to change in the temperature at which the flies were raised and type of culture container in which they bred were followed in the two inbred lines, Wellington (Well) and Samarkand (Sam). In respect of chaeta number Well was more sensitive to change of the environment than Sam, which furthermore responded in the opposite direction to Well. In respect of yield of offspring the two lines responded similarly. The genetic control of these responses to environmental change was investigated by using the eight substitution lines which comprise all the possible true breeding combinations of the three major chromosomes (X, II and III) from Well and Sam. Two experiments were carried out, the first a diallel experiment at three temperatures (18, 21.5 and 25 °C), and the second an experiment in which the eight lines were raised in nine environments comprising all combinations of the three temperatures and three types of culture. Chaeta number changes more with temperature than with type of culture, whereas the reverse is true of yield of offspring. In respect of chaeta number the genes chiefly responsible for response to environmental change are borne on a different chromosome (II) than those chiefly responsible for variation in mean chaeta number (III), and there are indications of a similar situation in respect of yield of offspring. It is concluded that different characters are separately adjustable by selection in their responses to enviromental change, that sensitivity of a character to environmental change is adjustable separately from mean expression of the character, and that the detailed patterns of response to a range of environments (e. g. temperatures) are separable from the magnitude of the overall change induced by these environments.


2009 ◽  
Vol 4 (1) ◽  
pp. 139
Author(s):  
Philip Teguh Imanto

Keberhasilan pembenihan ikan sangat dipengaruhi keberhasilan produksi jasad pakan rotifer secara tepat dan efisien. Penelitian kultur rotifer dengan tangki volume kecil bertujuan untuk mendapatkan efisiensi produksi yang paling optimal dan memenuhi prinsip dasar akuakultur low volume high density. Penelitian menggunakan tangki polyethylene dengan volume 500 L dan volume media awal 100 L, padat tebar awal 200 ind. rotifer per mL dengan sediaan pakan dasar fitoplankton Nannocloropsis occulata, ragi roti (0,05 g/mio.rot./feeding) dan suplemen Scott emulsion (0,005 g/mio.rot./feeding). Penelitian dilakukan secara bertahap; tahap pertama (I) tanpa penambahan air laut, peningkatan volume hanya dari penambahan 15 L Nannochloropsis tiap hari sampai hari kelima, tahap kedua (II) dengan penambahan alga 40 L dan air laut 40 L; serta tahap ketiga (III) dengan menggandakan pemberian ragi roti. Hasil penelitian menunjukkan bahwa pada percobaan tahap I: total produksi rata-rata 122,37 x 106 ind. rotifer, pada tahap II: 97,67 x 106 ind. rotifer, dan pada tahap III: dicapai rata-rata total produksi tertinggi dengan 187,17 x 106 ind. rotifer per tanki kultur 500 L. Pengelolaan kultur pada tahap III memberikan hasil terbaik dengan simpangan terkecil antar tangki kultur ulangan, dan membuktikan sebagai pengelolaan terbaik untuk kultur rotifer dengan tangki volume kecil. Success of marine seed production is highly influenced by effective and efficient production performance of life food rotifer. Observation on rotifer culture using small volume tank was aimed to get the optimum production and efficiency, to fulfill the basic principle of aquaculture “low volume high density”. Polyethylene tanks of 500 L. were used as culture container, with initial 100 liter sea water as culture medium and initial density of 200 ind. rotifer per mL. N. occulata, baker yeast (0.05 g/mio.rotifer/feeding) and Scott emulsion (0.005 g/mio.rotifer/feeding) were used as basic feed, and applied differently among three trials. First trial without seawater addition, increasing volume of culture media was only from 15 L. of N. occulata within 5 days culture, second trial was done with addition of seawater of 40 L and 40 L of N. occulata every day; and the last trial with twice dosage of baker yeast from trial I and II. The result showed that the average total production from the first trial was 122.37 x 106 ind. rotifer and the second trial was decreased to 97.67 x 106 ind. rotifer. Highest average total production was achieved by the last trial with 187.17 x 106 ind. rotifer per culture tank 500 L. Culture management on the third trial gave the best result with the lowest deviation among replication tanks, and proved as the best management practice for small-scale culture container.


2004 ◽  
Vol 87 (5) ◽  
pp. 1115-1122 ◽  
Author(s):  
Andrew P Jacobson ◽  
Richard L Thunberg ◽  
Mildred L Johnson ◽  
Thomas S Hammack ◽  
Wallace H Andrews

Abstract Alternative methods of reducing oxygen during anaerobic enrichment in the Bacteriological Analytical Manual (BAM) Shigella culture method were evaluated and compared to the current and less practical GasPak® method. The alternative anaerobic methods included the use of reducing agents in Shigella broth and reducing culture container headspace volume to minimize atmospheric effects on oxygen concentration in Shigella broth during enrichment. The reducing agents evaluated were sodium thioglycollate, L-cystine, L-cysteine, titanium(III) citrate, and dithiothreitol, each at concentrations of 0.1, 0.05, and 0.01%. The use of Oxyrase for Broth® with the enrichment medium (Shigella broth) was evaluated at concentrations of 10, 20 and 30 μL/mL. Recoveries of chill- and freeze-stressed S. sonnei strains 357 and 20143 were determined with each anaerobic method, including the GasPak method, using inoculation levels ranging from 100 to 103 cells. For each anaerobic method, strain, inoculation level, and stress type, 5 replicate enrichments were evaluated by streaking to MacConkey agar for isolation. The numbers of cultures with each method from which S. sonnei was isolated were used to compare the alternative anaerobic methods to the GasPak method. The alternative anaerobic method with which chill- and freeze-stressed S. sonnei strains 357 and 20143 were isolated most consistently was the use of Oxyrase for Broth in Shigella broth at a concentration of 20 μL/mL. This method was compared to the GasPak anaerobic method in evaluations on the recovery of S. sonnei strains 357 and 20143 from artificially contaminated test portions of parsley, cilantro, green onions, strawberries, carrots, and celery. A third anaerobic method included the use of 0.5 cm mineral oil overlay on cultures containing Oxyrase for Broth at concentrations of 20 μL/mL. Recovery rates of strain 357 were significantly greater (p < 0.05) with the GasPak method than with Oxyrase for Broth, with and without the 0.5 cm mineral oil overlay, for test portions of parsley, cilantro, and celery. When Oxyrase for Broth was used with Shigella broth, strain 357 was isolated at higher rates from all produce types, except cilantro, when 0.5 cm mineral oil overlay was applied to enrichment cultures. The use of mineral oil overlay with Oxyrase for Broth also improved recovery of strain 20143 from test portions of all produce types except green onion and strawberries. These differences were significant (p < 0.05) with parsley, carrots, and cilantro (1 of 2 evaluations). No statistically significant differences (p > 0.05) between the GasPak and Oxyrase for Broth anaerobic methods occurred when mineral oil overlay was used with Oxyrase for Broth. The use of Oxyrase for Broth with a 0.5 cm mineral oil overlay is a practical alternative for anaerobic enrichment with the BAM method in the analysis of some produce types. Differences in recovery among the different produce types and methods occurred between S. sonnei strains 357 and 20143, emphasizing the need for additional S. sonnei strains in future evaluations.


2007 ◽  
Vol 2 (3) ◽  
pp. 307-325 ◽  
Author(s):  
Will Minuth ◽  
Lucia Denk ◽  
Kanghong Hu ◽  
Hayo Castrop ◽  
Celso Gomez-Sanchez

AbstractLittle is known about the extra- and intracellular stimuli inducing renal stem/progenitor cells to develop into three-dimensionally structured tubules. To study this specific development in a controlled environment, we used an advanced culture technique. Embryonic tissue derived from neonatal rabbit kidney was placed in a perfusion culture container at the interface of an artificial interstitium made of a polyester fleece. Culture was carried out in chemically defined Iscove’s Modified Dulbecco’s Medium (IMDM) for 13 days. Development of tubules was histochemically detected on cryosections labeled with Soybean Agglutinin (SBA). The experiments showed that aldosterone exerts a specific tubulogenic effect. Application of aldosterone (1 × 10−7 M) raised numerous SBA-labeled tubules, while in the absence of the steroid hormone the development of tubules was lacking. Specificity of hormone action was analyzed by the use of aldosterone antagonists. Administration of spironolactone (1 × 10−4 M) and canrenoate (1 × 10−5 M) completely inhibited the development of tubules. Finally, disrupting the intracellular molecular complex of the mineralocorticoid receptor (MR) and heat shock proteins by geldanamycin (2 μg/ml) prevented the development of tubules. Our results suggest that the tubulogenic effect induced by aldosterone is attributed to both hormone binding and an undisturbed intracellular response of the MR.


2018 ◽  
Vol 7 (1) ◽  
pp. 763
Author(s):  
Suryo Kunindar ◽  
Eko Efendi ◽  
Supono Supono

Liquid waste produced by tofu and tapioca industry was approximately 1,5-2 m3 and 4-6 m3 per day respectively. Tapioca liquid waste has concentration of carbon around 119,11 mg/l, while tofu liquid waste has around 133,03 mg/l of nitrogen in concentration. Therefore both of these waste have the potential to be used as biofloc that utilized as additional feed with high protein content for nile tilapia. The aim of this research was to know interaction between C/N ratio and place of biofloc production to the growth of nile tilapia. This research used completely randomized design based on factorial experiment which consisted of two level of each factor and three repetition. Level of C/N ratio were 15 and 20 whereas level of place of biofloc production were inside and outside fish culture container. The result of this research showed that interaction between place of biofloc production and C/N ratio affected the growth of nile tilapia. The treatment inside biofloc production with 20 C/N ratio gave provided the highest absolute growth (3,26 g) and daily growth rate (0,082 g per day).


2020 ◽  
Vol 3 (1) ◽  
pp. 15-18
Author(s):  
Nur Achmad Saputra ◽  
A. Gusti Tantu ◽  
Machuluddin Amin ◽  
Dahlifa Dahlifa ◽  
Sutia Budi

Pertumbuhan fitoplankton dipengaruhi oleh beberapa faktor fisika seperti suhu, cahaya matahari, kedalaman, kekeruhan, salinitas, dan kandungan oksigen, faktor kimia seperti pH, fosfat, nitrat, nitrit, dan silikat serta warna wadah kultur. Tujuan penelitian untuk mengetahui pengaruh warna wadah terhadap pertumbuhan Nanochloropsis sp. Penelitian didesain menggunakan Rencana Acak Lengkap (RAL). Perlakuan yang diuji adalah penggunaan wadah kultur yang memiliki warna berbeda dengan empat perlakuan dan tiga kali ulangan. Warna wadah yang digunakan adalah merah, kuning, biru dan bening. Hasil penelitian menunjukkan penggunaan warna wadah berpengaruh nyata terhadap pertumbuhan Nannochloropsis sp. Warna wadah terbaik untuk pertumbuhan Nannochloropsis sp. adalah bening. Phytoplankton growth is influenced by several physical factors such as temperature, sunlight, depth, turbidity, salinity, and oxygen content, chemical factors such as pH, phosphate, nitrate, nitrite, and silicate as well as the color of the culture container. The purpose of the study was to determine the effect of container color on the growth of Nanochloropsis sp. The study was designed using a Completely Randomized Plan (CRD). The treatment tested was the use of culture containers that had different colors with four treatments and three replications. The color of the container used is red, yellow, blue and clear. The results showed that the use of container color significantly affected the growth of Nannochloropsis sp. The best container color for the growth of Nannochloropsis sp. is clear.


2019 ◽  
Vol 6 (2) ◽  
pp. 89
Author(s):  
Nur Ajijah ◽  
Cici Tresniawati ◽  
Syafaruddin Syafaruddin

<p><em>Container culture have an important role in determining the success of in vitro culture since it will affect the development of culture, such as the formation of embryonic structures. The study aimed to determine the effect of culture container types on cacao somatic embryogenesis. The study was conducted at Tissue Culture Laboratory, Superior Seed Development Unit of IAARD, Bogor, from April to September 2016. The tests were conducted on the effect of container and explant types as well as the effect of container types and genotypes. The effects of container and explant types were tested using callus induced from petal and staminoid explants of Sca 6, whereas the effects of container types and genotypes were tested using callus induced from petal explants of Sca 6 and ICCRI 4. Afterwards, the somatic embryos were induced using petri dishes or culture bottles according to treatment. The results showed no significant interaction between container and explant types on the average percentage of the formation and number of somatic embryos (10.28% embryos/explants in culture bottles and 7.89% embryos/explants in petri dishes). Meanwhile, there was significant interaction between genotypes and container types in the initial period of somatic embryos formation (15 and 18 weeks after culture), but the effect was not significant in the final period of observation (21 weeks after culture). The results indicate that culture bottles, which have lower prices, can be used to replace petri dishes to induce the formation of somatic embryos in cacao.</em></p>


HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 630f-630
Author(s):  
Carol D. Robacker

Previous studies indicated that the number of shoots formed per nodal explant varied significantly depending upon the type of culture container used. Amount of media per container and amount of time that media was autoclaved were variables that differed among the containers. To determine the cause for the container effect on shoot number, a study was conducted in which autoclave time and amount of media per container were the same for all tested containers. Media was autoclaved in 500-mL batches for 30 min, then poured in 30-mL aliquots into sterile containers. Containers tested were plastic petri plates, GA-7 Magenta vessels and glass jars. Depth of the medium was 5 mm in plates, 8 mm in vessels, and 12 mm in jars. Nodes from in vitro grown shoots of `Triumph', `Regale', and `Fry' were cultured on Murashige and Skoog salts and vitamins with 2 mg·L–1 BA and 8 g·L–1 agar. Results indicated that the greatest number of shoots formed in the jars. In a second study, nodes were cultured on petri plates containing 30 mL of medium (depth 5 mm) or 70 mL (depth 12 mm). Two to three times more shoots formed on the plates with the greater amount of medium. These studies indicate amount and depth of medium are factors influencing shoot number.


2020 ◽  
Vol 9 (2) ◽  
pp. 155
Author(s):  
Lutfiyah Al Adawiyah ◽  
Mohammad Faizal Ulkhaq ◽  
Hapsari Kenconojati

Utilization of Porphyridium sp. began to be developed as an anticancer, anti-inflammatory, antibacterial, antifungal, and production of biogas and biodiesel so that necessary to carry out culture activities for ensure continuity of Porphyridium sp. This study aims to determine the type of culture container that showed the best growth response of Porphyridium sp. with the highest biomass. The stages in this research were preparation of containers and media sterilization, making diatom fertilizers and agar media, Culture of Porphyridium sp. on agar media, Culture of Porphyridium sp. in the test tube, and Culture of Porphyridium sp. in glass and plastic containers. The results showed that the growth response of Porphyridium sp. that cultured in glass containers (18,9 ± 0,21 x 105 cells/mL) was higher than plastic (15.57 ± 0,03 x 105 cells/ml).


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