• Title/Summary/Keyword: incubation method

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Studies on Water Metabolism in Developing Chick Embryos - II. Water Distribution to Different Tissues and Organs of Developing Chick Embryos in Various Incubating Stage (부화계태아의 수분대사에 관한 연구 - II. 부화일령에 따른 계태아의 각조직 및 기관에 대한 수분분포)

  • Kim Young-Hong
    • Journal of the korean veterinary medical association
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    • v.16 no.4_5
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    • pp.193-198
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    • 1980
  • The studies were under taken with the objective to observe water distribution and its content of developing embryo by dry method during the incubation periods. The results obtained were summarized as follows: 1. For the first time each developing embryoni

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Studies on Water Metabolism in Developing Chick Embryos - I. Water Division of Developing Chick Embryos in Various Incubating Stages (부화계태아의 수분대사에 관한 연구 - I. 부화일령에 따른 계태야의 수분분할)

  • Kim Young-Hong
    • Journal of the korean veterinary medical association
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    • v.16 no.4_5
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    • pp.189-192
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    • 1980
  • The studies were undertaken with the objective to observe water distribution and its content in egg during the incubation periods by dry method. The resalts obtained were sammarized as follows: 1. Chick embryo was not recogenizable on second and third day

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NOS(Nitric Oxide Synthase) 작용 검색법

  • 이종화
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1993.04a
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    • pp.151-151
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    • 1993
  • A. 1. 중추신경계에서 일어나는 병변들, Alzheimer's disease, Parkinsonism 및 정상적인 노화현상들을 구명하는 연구의 일부분으로 뇌내의 신경세포들의 세포내물질의 변화를 관찰하고자, 이 실험을 시도하였다. 2. 중추신경계에 작용하는 각종 약물들의 작용기전, 그리고 부작용을 구명하여 그의 예방 및 치료방법을 모색하고자 한다. B. 1.Preparations: rat brain cytosol & culture cell-line(NIE-115) 2. Method: NO or NOS의 생성함량을 직접측정 할 수 없으므로 간접방법을 택한다. [3Hlarginine 및 [3Hlguanine을 Preparation에 incubation시켜 일정한 시간 후 생성되는 [3H]citrulline 또는 cyclic GMP을 scintillation counter로 측정하여 그 함량으로 NO or NOS의 생성을 측정한다.

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Plant Regeneration from Mesophyll Protoplast of Nicotiana africana (Nicotiana africana의 엽육 원형질체로부터 식물체 재분화)

  • 최상주;이승철
    • Journal of the Korean Society of Tobacco Science
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    • v.15 no.2
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    • pp.130-136
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    • 1993
  • Protoplasts of palisade cells were aseptically isolated from leaves of Nicotiono apicona Merxm. by the one step enzymatic method. Efficiency of colony formation were depended on cell density and light condition during incubation, but an intensity of 47 ft-c during a period of 2 weeks after isolation of the protoplasts in the Nagata and Takebe's medium promoted the planting efficiency. Protoplast - derived calli of N. africana can be differentiated into shoot when cultured on Murashige and skoog's medium containing IAA(0.Smg/$\ell$) and zeatin(5.0mg/$\ell$).

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Xylanase Activity of Bacillus pumilus H10-1 Isolated from Ceratotherium simum Feces (흰 코뿔소 배설물로부터 분리한 Bacillus pumilus H10-1의 Xylanase 활성)

  • Yoon, Young Mi;An, Gi Hong;Kim, Jung Kon;Ahn, Seung-Hyun;Cha, Young-Lok;Yang, Jungwoo;Yu, Kyeong-Dan;Moon, Youn-Ho;Ahn, Jong-Woong;Koo, Bon-Cheol;Choi, In-Hoo
    • KSBB Journal
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    • v.29 no.5
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    • pp.316-322
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    • 2014
  • Xylanase have been used to convert the polymetric xylan into fermentable sugars from the production of ethanol and xylitol from plant biomass. The aim of this study was to isolate and identify xylanolytic bacterium from herbivore feces and was to used the xylanase for enzymatic hydrolysis of biomass. Xylanolytic strains were isolated from 59 different feces of herbivores from Seoul Grand Park located in Gwacheon Gyeonggi-do. The xylanolytic strains were selected by congo red staining and DNS method. Total 67 strains isolated from the herbivores feces were tested for xylanase activity. Among the strains, H10-1, which has the highest xylanase activity, was isolated from feces of Ceratotherium simum. The H10-1 strain was identified as Bacillus pumilus based on its morphological/biochemical characteristics and partial 16S rDNA gene sequences. Culture conditions of B. pumilus H10-1 such as initial medium pH, incubation temperature and incubation time were optimized for maximum xylanase production. And also xylanase produced by B. pumilus H10-1 was applied for the saccharification of Miscanthus sacchariflorus cv. 'Geodae 1', which was pretreated with 1.5M NaOH. The optimized culture conditions of B. pumilus H10-1 were pH 9, $30^{\circ}C$ incubation temperature, and 7 day incubation time, respectively. This xylanase activity under the optimized conditions was $20.4{\pm}3.3IU$. The crude xylanase produced by B. pumilus H10-1 was used for the saccharification of xylan derived from pretreated 'Geodae 1'. The saccharification conditions were $50^{\circ}C$, 200 rpm, and 5 days. Saccharification efficiency of pretreated 'Geodae 1' by B. pumilus H10-1 was 8.2%.

Effects of Lactose and Yeast on the Changes of Oligosaccharides during the Fermentation of Soy Yogurts (Lactose와 효모의 첨가가 대두요구르트 발효 중 올리고당의 변화에 미치는 영향)

  • Park, Mi-Jung;Lee, Sook-Young
    • Korean Journal of Food Science and Technology
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    • v.29 no.3
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    • pp.539-545
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    • 1997
  • Lactobacillus bulgaricus and Kluyveromyces lactis were inoculated to Jangyeob and Jinpum soy milks together after the addition of different amounts of lactose to increase the contents of oligosaccharides, which were compared with single cultured samples. The contents of stachyose, raffinose, sucrose, and glucose of samples without lactose decreased by single culture method, but the oligosaccharides decreased less than in single cultured samples containing of lactose. The oligosaccharides of single cultured samples were equal or decreased compared with soy milks. While those of mixed cultured Jangyeob and Jinpum samples containing 2% lactose for 24 hr incubation increased 125.0% and 118.1%, respectively and those of samples for 36 hr incubation increased 127.0% and 141.0%, respectively, those of mixed cultured samples containing 4% lactose for 24 hr incubation increased 112.5% and 123.0%, respectively and those of samples for 36 hr incubation increased 120% and 135.9%, respectively. Therefore, the oligosaccharides in samples containing 2% lactose were slightly more than in samples containing 4% lactose. Among the cultured methods, oligosaccharides were produced in the largest amounts by the mixed culture for 36 hr. The addition of lactose in soy milks for soy yogurts was effective in the formation of oligosaccharides since the galactose, produced by the hydrolysis of lactose, was thought to be combined with sucrose by the action of ${\beta}-galactosidase$ in yeast.

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The Dose-Dependent Effects of Nitric Oxide on Human Sperm Cell Function (Nitric Oxide가 인간 정자세포의 기능에 미치는 효과에 대한 연구)

  • Joo, Bo-Sun;Moon, Hwa-Sook;Park, Sue-Jin;Moon, Jae-Yeoun; Cho, Jae-Dong;Kim, Han-Do
    • Clinical and Experimental Reproductive Medicine
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    • v.25 no.1
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    • pp.43-50
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    • 1998
  • This study was performed to determine the effects of nitric oxide on human sperm cell function. Semen samples were obtained from normal healthy volunteers. Motile spermatozoas collected by swim-up method were incubated up to 24 hours in Ham's F-10 medium supplemented with a various concentration of sodium nitroprusside (nitric oxide releasing agent). Sperm motility, hyperactivation, acrosome reaction rate, and acrosin activity were determined. The results are as follows; 1. 1mM of SNP resulted in a significant decrease in sperm motility ($44.8%{\pm}8.9%:78.1%{\pm}6.3%$, and hyperactivation $(10.4%{\pm}6.4%:47.7%:{\pm}9.5%)$ after incubation for 3 hours compared with the control group (Ham's F-10 alone), but had no effect on acrosome reaction. 2. At $100{\mu}M$ SNP, sperm motility was reduced after incubation for 6 hours $(54.8%{\pm}3.2%)$ compared with that of the control group $(82.7%{\pm}8.9%)$, but hyperactivation and acrosome reaction were not affected. 3. However, a lower concentration (less than $10{\mu}M$) of SNP had no effect on sperm motility and hyperactivation for 8 hours of incubation but significantly decreased them when incubation periods were increased up to 24 hours compared with the control group. On the other hand, $1{\mu}M$ and $10{\mu}M$ SNP significantly increased the acrosome reaction rate in both acrosomal status ($17.3%{\pm}5.2%$, $23.5%{\pm}4.7%$, respectively) and acrosin activity ($34.3{\mu}IU{\pm}10.5{\mu}IU,\;45.6{\mu}IU{\pm}5.6{\mu}IU$, respectively) as compared with the control group $(7.0%{\pm}4.0%,\;9.5{\mu}IU{\pm}3.4{\mu}IU)$. These results indicate that SNP, NO releasing agent, has a dose-dependent effects on the sperm cell function. Therefore it may positively affect the fertilization by promoting acrosomal reaction at a lower concentration (less than $10{\mu}M$).

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Algal Growth Potential (AGP) Assay Using Heterosigma akashiwo(Raphidophyceae) in Pukman Bay, Korea (Heterosigma akashiwo(Raphidophyceae)을 이용한 북만의 조류성장잠재력 시험)

  • Kim Mu-Chan
    • Journal of the Korean Society of Marine Environment & Safety
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    • v.12 no.2 s.25
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    • pp.81-87
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    • 2006
  • Algal growth potential(AGP) assay using Heterosigma akashiwo was conducted in Pukman Bay. The effects of nutrients and microorganisms on the growth of H. akashiwo were specifically evaluated by the algal bioassay method. The different types of growth response of H. akashiwo to the addition of nutrients, and the co-incubation with microorganisms were clearly observed. Before H. akashiwo red tide occurrence, the growth of H. akashiwo was significantly stimulated by addition of nitrate of $50{\mu}M$ with phosphate of $5{\mu}M$. The addition of single phosphate had no clear effect on the growth of H. akashiwo. And the co-incubation with microorganisms had no clear effect on the growth of H. akashiwo. This result indicates that nitrate potentially limited the growth of H. akashiwo before red tide occurrence. However, during a bloom of H. akashiwo, the growth was significantly stimulated by addition of either nitrate of $50{\mu}M$ or phosphate of $5{\mu}M$. The addition of trace metals and vitamin $B_{12}$ had no clear effect on the growth of H. akashiwo in the period. This result indicates that both nitrate and phosphate potentially limited the growth of H. akashiwo during the bloom. On the other hand, during the termination period of H. akashiwo bloom, the growth of H. akashiwo was slightly stimulated by addition of phosphate and nitrate. But the growth of H. akashiwo was significantly enervated by the co-incubation with microorganisms. This result indicates that microorganisms potentially limited the growth of H. akashiwo in the period of bloom termination.

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Optimal culture methods for plant regeneration via shoot organogenesis in the 'Fuji' apple (사과 '후지'의 기관형성을 통한 식물체 재생에 효율적인 배양방법)

  • Yoon Kyung Lee;Youngju Kwon;Yong Joon Yang
    • Journal of Plant Biotechnology
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    • v.50
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    • pp.176-182
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    • 2023
  • Plant regeneration protocols for adventitious shoot organogenesis from apple (Malus domestica 'Fuji') leaf explants were developed in the present study. The effects of dark incubation periods in the early stages of culture, pre-treatment methods, the number of explants per culture container, the type of culture containers, and the orientation of the explants on culture media were evaluated to determine the optimal shoot regeneration conditions for 'Fuji' apple leaf explants. Light incubation of explants produced minimal response. However, dark incubation of explants for 4 weeks during the initial culture period enhanced shoot regeneration frequency. Comparing the number of explants per container, a higher percentage of shoot regeneration was obtained with nine explants per container compared with four explants per container. Pre-treatment, before culture, by dipping explants in a liquid regeneration medium containing 40 g/L of sorbitol for 2 hours produced the highest shoot formation rate, and the time of shoot formation was accelerated. The percentage of shoot regeneration and number of shoots per regenerating explant reached a maximum of 87.5% and 4.7, respectively. The regenerated shoots were elongated and rooted on a rooting medium of 1/4 MS with 0.2 mg/L IBA. The plantlets were successfully acclimatized, and the regenerated plants produced normal phenotypes.

Electroless Deposition and Surface-Enhanced Raman Scattering Application of Palladium Thin Films on Glass Substrates

  • Shin, Kuan Soo;Cho, Young Kwan;Kim, Kyung Lock;Kim, Kwan
    • Bulletin of the Korean Chemical Society
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    • v.35 no.3
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    • pp.743-748
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    • 2014
  • In this work, we describe a very simple electroless deposition method to prepare moderate-SERS-active nanostructured Pd films deposited on the glass substrates. To the best of our knowledge, this is the first report on the one-pot electroless method to deposit Pd nanostructures on the glass substrates. This method only requires the incubation of negatively charged glass substrates in ethanol-water mixture solutions of $Pd(NO_3)_2$ and butylamine at elevated temperatures. Pd films are then formed exclusively and evenly on glass substrates. Due to the aggregated structures of Pd, the SERS spectra of benzenethiol and organic isonitrile could be clearly identified using the Pd-coated glass as a SERS substrate. This one-step fabrication method of Pd thin film on glass is cost-effective and suitable for the mass production.