• 제목/요약/키워드: Sterile medium

검색결과 62건 처리시간 0.025초

구강암에 대해 항암효과를 나타내는 methanol 자화 방선균의 분리 및 동정 (Isolation and Identification of Methylotrophic Actinomycetes capable of Producing Anti-oral Cancer Activity)

  • 김정;김선숙
    • 한국치위생학회지
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    • 제1권2호
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    • pp.193-200
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    • 2001
  • An appropriate amount of samples, collected from three each paddy forest, field and riverside soil near Taegu city, was suspended in sterile water and then diluted in order to isolation of antagonistic to oral cancer. The diluted samples were inoculated on separating medium in the routing spreading method. So, seven hundred and eighteen strains were isolated on HV agar and 220 strains were on methanol medium from soil samples. So, during the screening of anti-oral cancer activity from soil, we isolated microorganisms showing powerful antagonistic activity. Among them, No. 78 strain exhibited the most strongly anti-oral cancer activity. Microbiological properties were investigated by the methods described in the Bergey's Manual of Systematic Bacteriology and experimental methods of identification of actinomycetes by Hamada et al. As a result, a methylotrophic actinomycetes strain No. 79 was estimated as Amycolatopsis sp. based on taxonomic studies.

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Establishment of Cell Suspension Cultures and Plant Regeneration in White Dandelion (Taraxacum coreanum NAKAI.)

  • Sun, Yan-Lin;Kim, Jae-Hak;Hong, Soon-Kwan
    • 한국자원식물학회지
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    • 제24권3호
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    • pp.280-285
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    • 2011
  • In this study, we established a novel somatic embryogenesis and plant regeneration system through cell suspension culture of white dandelion (Taraxacum coreanum NAKAI.). Embryogenic calli could be initiated from leaf and root explants of sterile seedlings on solid Murashige and Skoog (MS) medium supplemented with 1.0 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) after 3-week cultures. To proliferate embryogenic calli rapidly, cell suspension culture was performed with transferred to liquid MS medium with various combinations of plant growth regulators (PGRs) including 2,4-D, ${\alpha}$-naphthalene acetic acid (NAA), indole-3-acetic acid (IAA), $N^6$-benzylamino purine (BAP), thidiazuron (TDZ), and kinetin. During suspension cultures, embryogenic calli not only greatly proliferated, but shoot organogenesis also simultaneously occurred from the surface of somatic embryos. Among them, TDZ at lower concentration, 0.1 mg/L produced the highest efficiency of somatic embryo formation and shoot organogenesis. Rooting of embryogenic calli with adventitious shoots was done on solid MS medium containing 0.1 mg/L NAA and 0.3% activated carbon. Nearly 80% of embryogenic calli with shoot organogenesis could be rooted normal. Well-rooted plantlets were transferred into pots under a greenhouse condition, and plants derived from this system appeared phenotypically normal.

웅성불임기술을 이용한 쇠파리 구제에 관한 연구 1) 쇠파리의 인공대량사육에 관하여 (Study on Stable Fly Eradication by :Sterile-Male Technique. 1) Mass Rearing of the Stable Fly. Stemoxys calcitrans L.)

  • 정규회;유준;김용래;권신한;박정덕;강태숙
    • 한국응용곤충학회지
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    • 제12권1호
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    • pp.41-46
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    • 1973
  • 1) 쇠파리의 누대 실내사육을 위한 온도는 약 $26^{\circ}C$가 좋으며, 이때 유충기간은 약 6.8일, 용기간은 5.3일, 산란전기간은 10.4일, 성충의 수명은 약 30일이었다. 2) 인공사육에 있어서 용화율은 $80.7\%$ 우화율은 $84.3\%$였으며 성비는 1 : 1이었다. 3) 용의 체중량은 약 14.5mg이었으며, Wheat bran medium 보다 Standard medium이 사육성적이 좋았다. 4) medium 125gr에 대한 난의 접종수는 약 310개가 가장 적합하였다. 5) rectangular cage를 사용할 경우, 성충의 resting place는 $2inch^2/adult$가 적합할 것으로 본다.

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녹두 갈색무늬병균(Cercospora canescens Ellis & Martin)의 분생포자 형성에 관한 연구 (Sporulation or Cercospora canescens Ellis & Martin in culture)

  • 권신한;오정행
    • 한국응용곤충학회지
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    • 제20권1호
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    • pp.21-24
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    • 1981
  • 녹두 돌연변이계통의 갈색무늬병에 대한 저항성검정을 위하여 접종실험에 필요한 다량의 분생포자를 얻을 수 있는 배양조건 실험결과를 요약하면 다음과 같다. 1. 갈색무늬병균의 분생포자 형성에 적합한 배지는 기주식물조직배지인 녹두엽즙배지였으며 약 2500Lux의 형광조사는 분생포자 형성을 촉진시켰다. 2. 배양기상의 기중균사 거는 분생포자 형성을 현저히 증가시켜 OA배지에서도 MOA에서와 같은 량의 많은 분생포자 형성이 가능하였다. 3. 포자형성의 최적조건은 색소생성 및 균사장의 최적조건과 일치하지 않는 것으로 보였다.

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Cryopreservation of Capsicum annum var. grossum using encapsulation/dehydration of apices produced in vitro

  • Senarath, Wtpsk;Lee, Kui-Jae;Rehman, S.;Lee, Wang-Hyu
    • 한국자원식물학회:학술대회논문집
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    • 한국자원식물학회 2002년도 제9차 국제심포지움 및 추계정기학술발표회
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    • pp.53-53
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    • 2002
  • Shoot tips of in vitro propagated plantlets were cryopreserved using encapsulation/dehydration procedures. Shoot tips were excised under filter sterilized antioxidants solution (0.2M phosphate buffer, pH 5.7 supplemented with 5g/1 ascorbic acid and 15g/1 sodium borate). They were drawn up into a sterile 10 $\textrm{cm}^3$disposable pipette and were dropped into the culture medium with 2.5w/v Na-alginate, then into 100mM CaCl$_2$.2$H_2O$. Encapsulated shoot tips were transferred into 10㎤ of liquid culture medium with a range of sucrose concentrations (0.25-1.0M) and were incubated in dark for 24 hours in 18C at 40rpm. Beads were then dehydrated in silica gel for different time intervals (1-24 hours). Then they were freeze dried either rapidly (plunge directly into liquid N2 or in two stages (samples were kept at 20C for 10 minutes, then reduced to 35C at 1C per minute. Then, plunge into liquid $N_2$). The influence of sucrose and silica gel pre-treatment on pre- and post-freeze shoot growth was examined.(중략)

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An Efficient Micropropagation to Obtain the Disease-free Bulbs from Scales for Cryopreservation in Lilium

  • Song, Jae-young;Yi, Jung-yoon;Yoon, Mun-sup;Lee, Jung-ro;Lee, Young-yi
    • 한국자원식물학회:학술대회논문집
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    • 한국자원식물학회 2019년도 추계학술대회
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    • pp.37-37
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    • 2019
  • Cryopreservation is one of the ideal and suitable methods for long-term storage of plant germplasm. The plant contaminated with diseases and pathogens are decreased the multiplication rate, survival rate and high quality of plants after cryopreservation. The aim of this work was to improve a micropropagation method for lily in Korea, which are cultivars and indigenous plant. In the last process of rinsing scales after surface-sterilization, we tried to control the diseases and pathogens lived within the tissue by rinsing in 0.03% sodium hypochlorite (NaClO) instead of sterile distilled water. Bulb scales of Lilium were cultured in vitro on MS medium supplemented with Plant Preservative Mixture (PPM). The newly small bulb formed from bulb-scales was transferred to MS medium. We checked the non-contamination and survival rate after 2 weeks in culture. Non-contamination was shown to be 70 to 90% in formed small bulbs. This study will help to mitigate microbial contamination in Lilium species micropropagation for cryopreservation.

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Effects of Temperature and Moisture on the Survival of Colletotrichum acutatum, the Causal Agent of Pepper Anthracnose in Soil and Pepper Fruit Debris

  • Kang, Beum-Kwan;Kim, Joo-Hyeong;Lee, Kyeong-Hee;Lim, Sang-Cheol;Ji, Jae-Jun;Lee, Jong-Won;Kim, Heung-Tae
    • The Plant Pathology Journal
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    • 제25권2호
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    • pp.128-135
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    • 2009
  • The survival of Colletotrichum acutatum was investigated in soil, infected fruits, and infected fruit debris incorporated into soil at several temperatures with different soil moisture levels. Samples were examined at 2-week intervals for 18 weeks to determine the survival of the pathogen based on the number of colony forming unit (CFU) of C. acutatum recovered on a semi-selective medium. C. acutatum conidia survived in both sterile and non-sterile soil at 4 and $10^{\circ}C$ for 18 weeks. If infected pepper fruits were completely dried, C. acutatum survived for 18 weeks at temperature from 4 to $20^{\circ}C$. Soil temperature and moisture affected the survival of C. acutatum in infected fruit debris incorporated into soil after air-drying. The effect of soil moisture on survival was weaker at low temperatures than at high temperatures. For up to 16 weeks, conidia were recovered from fruit debris in soil that had been kept at 4 to $20^{\circ}C$ and below 6% soil moisture. Conidia were recovered from fields until approximately 6 months after pepper fruits were harvested. Using PCR with species-specific primers and a pathogenicity test, we identified conidia recovered from soil and infected fruit from both the laboratory and field as C. acutatum and as the primary inoculum causing pepper anthracnose.

Validation of aseptic processes for pharmaceuticals

  • Joseph, Lincy;George, Mathew;Jain, Saurabh Kumar
    • Advances in Traditional Medicine
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    • 제10권4호
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    • pp.231-238
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    • 2010
  • Sterile Products may be broadly classified into two main categories, according to the manner in which they are produced: those which are sterilized after the product has been filled and sealed in the final container(s) ("terminally sterilized" products) and those where the sterilization stage (or stages) takes place is it before or after the bulk product filled in to final container. In this latter instance, all subsequent processing (typically, the filling and sealing operations) must be conducted aseptically in order to prevent recontamination of the sterilized product. The two most common pharmaceutical applications of aseptic processing methods are (a) the filling of liquid products following sterilization by filtration and (b) the filling of previously sterilized bulk powder products. An aseptic processing operation should be tested using a microbiological growth medium (media fill) during lyophilized injection formulation, filling, loading, lyophilisation, stoppering, and unloading activities.

Impact of Massive Neutrinos and Dark Radiation on the High-Redshift Cosmic Web

  • Rossi, Graziano
    • 천문학회보
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    • 제43권1호
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    • pp.38.1-38.1
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    • 2018
  • With upcoming high-quality data from surveys such as eBOSS or DESI, improving the theoretical modeling and gaining a deeper understanding of the effects of neutrinos and dark radiation on structure formation at small scales are necessary, to obtain robust constraints free from systematic biases. Using a novel suite of hydrodynamical simulations that incorporate dark matter, baryons, massive neutrinos, and dark radiation, we present a detailed study of their impact on Lyman-Alpha forest observables. In particular, we accurately measure the tomographic evolution of the shape and amplitude of the small-scale matter and flux power spectra and search for unique signatures along with preferred scales where a neutrino mass detection may be feasible. We then investigate the thermal state of the intergalactic medium (IGM) through the temperature-density relation. Our results indicate that the IGM at z ~ 3 provides the best sensitivity to active and sterile neutrinos.

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Culture Characteristics of Streptomyces spp. on Improved Polyacrylamide Gel and Agar Media

  • Han, Hong ui;Baek, Ji-Ho;Yang, Moon
    • Journal of Microbiology
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    • 제34권4호
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    • pp.384-386
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    • 1996
  • Application of polyacrylamide gel (PAG) instead of agar to solid cultures of Streptomyces spp. was studied. The improved media were prepared by 1) gelling 20 ml of 5% acrylamide in a glass petri dish at room temperature, 2) washing by running water for more than 8 hr to remove residual reaction reagents, 3) drying at 5$0^{\circ}C$ for 12 hr to make a gel film, 4) autoclaving at 121$^{\circ}C$ for 15 min, and 5) swelling gel for about 4 hr by adding sterile liquid medium. In PAG media there were no differences from the observation of morphological characteristics showing during the cellular differentiation on agar media, whereas the ability to utilize carbohydrates differed somewhat from agar media. Agar media thus were little favorable for biochemical tests which the growth was determined depending on the formation of colony, but washed PAG was superior to serve as a solidifying agent.

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