• Title/Summary/Keyword: 2.5% sucrose

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Micromorphological Changes of Waterlogged Archaeological Wood in PEG4000 and Sucrose Treatment (수침출토목재에 PEG4000과 Sucrose처리에 따른 변화)

  • Kang, Ae Kyung;Park, Sang Jin
    • Journal of Conservation Science
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    • v.5 no.2 s.6
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    • pp.3-14
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    • 1996
  • The chemicals are PEG $\#4000$ and sucrose, which have been conventionally used for the treatment of waterlogged wood. The present investigation was undertaken in order to reveal difference of the impregnation between the chemicals, but also to contribute to the explanation of the chemicals penetration process and distribution within wood structure. Comparable observation concerning the deposits shapes of chemicals after treatment, PEG4000 penetrated samples were occurred at the cell wall shrinkage and cracks, whereas the majority of the cells and lumens were entirely filled with a crystalline structure. Sucrose penetrated samples remained almost like sound wood, although the penetration ristricted only the cell walls was filled by amorphous structure.

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Characteristics of Organic Wastewater Degradation on Hydrogen Fermentation (수소발효의 유기성 폐수 분해 특성)

  • 이영준
    • Journal of Environmental Health Sciences
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    • v.26 no.2
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    • pp.1-5
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    • 2000
  • 연속형 혐기성처리 반응조에서 배양된 수소발생 슬러지를 이용하여 증온 조건에서 회분식 혐기성 처리방법으로 유기성 폐수로부터 전환되는 수소가스 및 대사산물들에 대한 연구를 수행하였다. 수소발생에 대한 기질로는 sucrose를 이용하였다. 처리과정에서 발생된 누적수소가스, 휘발성지방산(VFAs) 및 solvents는 Gompertz equation을 이용한 비선형회귀분석을 통하여 계산하였다. 처리과정 중 수소가스는 반응초기에 발생하였고, 발생된 가스내 수소가스가 차지하는 비율은 약 20%이었다. 반응 전과정에서 메탄가스는 발생하지 않았다. 비수소가스발생율은 sucrose 농도가 40 g/l일 때 0.956 ml/g VSs/h이었으며, sucrose 농도가 300g/l의 경우는 0.011 ml/g VSS/h이었다. 수소가 발생하는 기간 동안 VFAs의 생성은 acetate, butyrate의 순으로 높게 생성되었으나, propionate로의 전환은 발견되지 않았다. solvents의 경우 butanol이 가장 높게 발생하였다.

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Effects of Fructo-Oligosaccharide and Isomalto-Oligosaccharide on Quality and Staling of Cake (올리고당의 첨가가 케\ulcorner揚\ulcorner 품질과 노화에 미치는 영향)

  • 김영애
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.27 no.5
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    • pp.875-880
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    • 1998
  • Fructo-oligosaccharide and isomalto-oligosaccharide were used to replace 10%, 20%, or 30% of the sucrose in cake. Replacement with either fructo-oligosaccharide or isomalto-oligosaccharide resulted in cakes with higher volume, browner crust, yellower crumb. Cakes baked with oligoaccharide were softer than 100% sucrose cake. During 9 days storage at 2$0^{\circ}C$, the hardness of both 10% fructooligosaccharide and 10% isomalto-oilgosaccharide cakes was higher than that of 20% and 30% oligosaccharide cake was higher than that of 10% fructo-oligosaccharide cake at the end of storage, there was no difference in hardness among 10%, 20% and 30% isomalto-oligosaccharide cakes. Cakes substituted with isomaltooligosaccharide for sucrose at the level of 20% and 30% or with fructo-oligosaccharide at the level of 30% were significantly moist compared to control. Replacement of sucrose with oligosaccharide, except with fructo-oligosaccharide at the level of 30%, did not affect significantly overall likeness of cakes.

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수용성 황색색소를 분비하는 Bacillus sp. PY123균주의 분리 및 특성

  • 김지연;김광현
    • Microbiology and Biotechnology Letters
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    • v.25 no.5
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    • pp.454-458
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    • 1997
  • To develop a yellow pigment for a food-additive, a strain producing a water-soluble yellow pigment was isolated from phylloplane of tree leaf. The strain PY123 was identified a Bacillus sp. based on morphological and biochemical characterization such as a bacillus form, mortility, spore formation, Gram positive, and catalase production. The pigment production of the strain PY123 was increased about 3 times in patato broth containing 1% sucrose and 0.1 mM CoCl$_{2}$ than in only potato broth after incubation at 30$circ$C, for 2 days. When 0.1 mM CoCl$_{2}$, was added in potato broth containing 1% sucrose at late log phase during incubation of the strain PY123, cell growth was not inhibited, and the period at maximal pigment production of the strain PY123 was about 12hrs faster than in potato broth containing 1% sucrose and 0.1 mM CoCl$_{2}$, simultaniously.

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Proliferation of Embryogenic Callus of Kalopanax pictus through Suspension Culture System (현탁배양을 통한 음나무(Kalopanax pictus) 배발생 캘러스의 증식)

  • Kim, Hye-Jin;Kim, Won-Bea;Yoo, Dong-Lim;Kim, Su-Jeong;Lee, Jun-Gu
    • Korean Journal of Plant Resources
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    • v.21 no.1
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    • pp.60-65
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    • 2008
  • Kalopanax pictus was cultured in vitro to find out optimal condition for embryogenic cells proliferation in liquid media rapidly. Embryogenic cells were induced from leaves and petiols of Kalopanax pictus. Optimum culture medium appeared to be a 1/2MS medium supplemented with 2.0mg/L 2,4-D and 0.1mg/L BA. To find out optimal conditions, embryogenic cells were cultured some condition as different concentrations of 2,4-D, medium and sucrose. There was cultured on 1/2MS liquid medium containing different concentration of 2,4-D. When embryogenic cells were cultured on 1/2MS liquid medium supplemented with 1.0mg/L 2,4-D, cell propagation rate was higher than other concentration of 2,4-D. When embryogenic cells were cultured on different media that MS, Gambols B5, N6, White, SH medium, observed the highest multiplication rate among Gambols B5 and White medium. To find out of effect of sucrose to embryogenic cells propagation, we tested cells under different concentrations. Optimal concentration of sucrose appeared to be a basal medium added 3% sucrose. Above results suggest that optimal conditions for proliferation of embryogenic cells were established Gambols B5 and White medium added 1.0mg/L 2,4-D and 3% sucrose. There is every possibility achieving embryogenic cells proliferation via bioreactor culture system in Kalopanax pictus.

In vitro shoot regeneration from leaf tissue of "Whangkeumbae" pear(Pyrus pyrifolia Nakai) (황금배(Pyrus pyrifolia Nakai) 잎 조직으로부터 기내 신초 재분화)

  • Chun, Jae An;Do, Kyung Ran;Kim, Se Hee;Cho, Kang-Hee;Kim, Hyun Ran;Hwang, Hae Sung;Shin, Il Sheob
    • Journal of Plant Biotechnology
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    • v.39 no.4
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    • pp.288-294
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    • 2012
  • In order to establish an efficient adventitious shoot regeneration conditions from leaf explants for Asian pear 'Whangkeumbae', the effect of concentration and kinds of plant growth regulator and carbon source was investigated. Leaf explants of cultures grown on Murashige and Skoog (MS) medium containing 8 g/L plant agar were used. When the medium contained 0.25 mg/L thidiazuron (TDZ) and 0.3 mg/L indolebutyric acid (IBA), the adventitious shoot regeneration rate (ASRR) was greater as 61.1% than others treated and higher TDZ concentrations (2.5 and 5 mg/L) treatment significantly reduced the ASRR. As the effect of IBA and indoleacetic acid (IAA) concentration on the ASRR, 0.5 mg/L TDZ plus different concentration of IAA exhibited relatively high ASRR and 0.5 mg/L TDZ plus 0.3 mg/L IAA showed the highest ASRR of 76.7%. Also the effect of sucrose and sorbitol as carbon source on regeneration was examined. The highest ASRR and the most shoots per explants averaged 94.4% and 3.49 by treatment of 30 mg/L sorbitol, respectably. Sorbitol is considered better carbon source than sucrose for shoot regeneration of 'Whangkeumbae' pear.

In Vitro Micropropagation of Chinese Yam (Dioscorea opposita Thunb.) through the Culture of Micro-tuber Sections and by Addition of Liquid Medium (영여자 절편체 배양 및 액체배지 첨가에 의한 둥근마의 기내 대량번식)

  • Kim, Young-Ho;Lim, Soon-Taek;Han, Bong-Hee
    • Korean Journal of Medicinal Crop Science
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    • v.20 no.3
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    • pp.190-194
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    • 2012
  • Shoot tips of chinese yam (Dioscorea opposita Thunb.) were cultured on MS medium containing 0.5 mg/L BA to produce micro-tubers in vitro. To stimulate the formation of shoots and micro-tubers, and produce large micro-tubers, the sections of micro-tubers were cultured on MS media with BA and IAA. The shoot multiplication, and the micro-tuber formation and growth were very effective on the media containing 2.0 mg/L BA and 0.5~1.0 mg/L IAA. Sucrose added to MS medium with 2.0 mg/L BA and 0.5 mg/L IAA to stimulate more micro-tuber growth. The medium added 50 g/L sucrose was very effective in the increase of plant fresh weight and micro-tuber growth. After 4 weeks' culture of micro-tuber sections on the medium with 2.0 mg/L BA, 0.5 mg/L IAA and 50 g/L sucrose, the liquid media were added into the same vessels. The micro-tuber growth was stimulated remarkably by the addition of liquid medium. The addition of 25 $m{\ell}$ liquid medium containing 10 g/L activated charcoal, 3x MS salts and 250 g/L sucrose was the most effective in micro-tuber growth.

Lactic Acid Fermentation of Soymilk by Mixed Cultures of Lactobacillus bulgaricus and Kluyveromyces fragilis (Lactobacillus bulgaricus 와 Kluyveromyces fragilis의 혼합배양에 의한 두유의 젖산발효)

  • Yu, Ju-Hyun;Lew, In-Deok;Park, Chung-Kil;Kong, In-Soo
    • Korean Journal of Food Science and Technology
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    • v.19 no.3
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    • pp.263-272
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    • 1987
  • Lactobacillus bulgaricus (KFCC 35463) and Kluyveromyres fragilis (KFCC 35458) were inoculated together in soymilk, and then growth characteristics, acid production and the conditions suitable for acid production were investigated. L. bulgaricus produced more acid and the rate of acid production was more rapid when this organism was incubated with K. fragilis in soymilk than when it was incubated singly. Studying the conditions suitable for acid production in soymilk, optimum acid production by the mixed cultures of L. bulgaricus and K. fragilis was achieved with a temperature of $35{\sim}37^{\circ}C$, a 1:2 (O.D.660) ratio of L. bulgaricus to K. fragilis at inoculum, a 1.0% level of sucrose fortification or a 1.5% level of skim milk powder fortification and a culture time of 24hr. Under these conditions the amount of acid produced by the single culture of L. bulgaricus and the mixed cultures of L. bulgaricus and K. fragilis were 0.14% and 0.41%, respectively, in soymilk, 0.13% and 0.70%, respectively, in soymilk fortified with 1.0% level of sucrose. These indicate that the amount of acid produced by mixed cultures is about 2.9-fold greater in soymilk and about 5.4-fold greater in soymilk fortified with 1.0% level of sucrose than that produced by the single culture of L. bulgaricus. The amount of acid produced in soymilk fortified with 1.5% level of skim milk powder was 0.84% level for both of the single culture of L. bulgaricus and the mixed cultures of L. bulgaricus and K. fragilis after 24hr incubation. However, the amount of acid produced by the mixed culture with K. fragilis was greater than that produced by the single culture of L. bulgaricus onlv in soymilk fortified with lower levels of skim milk powder than 1.5%.

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Studies on the Effect of 2-Chloroethylphosphonic Acid (Ethephon) on the Floral Induction in Photoperiodic Plants (광주기식물의 개화유도에 미치는 2-Chloroethylphosphonic Acid(Ethephon)의 효과에 관한 연구 I. Ethephon에 의한 Lemna perpusilla 6746 개화억제)

  • 맹주선
    • Journal of Plant Biology
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    • v.20 no.2
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    • pp.77-82
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    • 1977
  • The inhibiotory effect of ethphon on the flowering in Lemna perpusilla 6746 was shown to be related to sucrose concentrations and dilution factors of Hutner's medium. When grown in 1/10-strength Hutner's medium under 10(14) cycles, the plants have been completely inhibited in the floral induction by ethephon (>5ppm) in the presence of sucrose (>20 mM) in the meduim. However, in a less diluted Hutner's medium (1/2-strength), the inhibition of flowering by ethephon was observed to be partially diminished by sucrose at a high concentration (30mM), while a low concentration of sucrose enhanced the inhibitory effect of ethephon in flowering. As inductive dark periodswere extended, the effects of both compounds were partially nullified. Since no significant amount of ethylene possibly released in ethephon decomposition in the medium was detected, the inhibitory effect of ethephon in flowering was postulated to be exerted only through ethylene production within the plants. Plants were incubated in 10 ppm ethephon-containing medium during either dark or light periods, singly or periodically. The most effective single treatment with ethephon was observed during the 4th dark period, when formation of floral stimulus was assumed to be completed beyond a critical level. This postulation can be partially supported by a fact that the plants should be exposed to at least more than four consecutive 10(14) cycles for flowering.

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Purification and Characterization of an Extracellular Levansucrase from Zymomonas mobilis ZM1(ATCC 10988). (Zymomonas mobilis ZM1이 생산하는 균체외 Levansucrase의 정제 및 특성)

  • 송기방;서정우;주현규;이상기
    • Microbiology and Biotechnology Letters
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    • v.26 no.4
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    • pp.309-315
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    • 1998
  • An extracellular levansucrase, which catalyzes the formation of levan from sucrose, from the culture broth of Zymomonas mobilis ZM1 was purified by conventional column purification methods. The final purification yield was 18.3 fold of the crude enzyme from Z. mobilis, with 16.5 % of the enzyme recovered in the preparation step. The molecular weight of the enzyme was estimated to be 91,000 by Superose 12 gel filtration, and 45,000 by SDS-PAGE, indicating that levansucrase is a dimer. The optimum pH for the enzyme activity was around pH 4.0 for sucrose hydrolysis, and was around pH 5.0 for levan formation. The enzyme was inhibited by some metal ions, such as Hg$\^$2+/ and Cu2$\^$2+/, and 50% of inhibition was observed with 5mM EDTA. The enzyme activity was enhanced by the presence of detergent Triton X-100, but inhibited by SDS completely The enzyme catalyzes the liberation of reducing sugars, oligosacccharides and the formation of fructose polymer(levan). The enzyme also catalyzes the transfructosylation reaction of fructose moiety from sucrose to various sugar acceptor molecules, including sugar alcohols.

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