• 한국버섯학회지
• /
• 제13권1호
• /
• pp.50-55
• /
• 2015

본 연구에서는 꽃송이버섯 건물과 powder를 각각 Yeast Extract broth와 MRS broth에서 Lactoballius 4종(L. plantarum, L. acidophilus, L. helveticus, and L. delbrueckii)과 함께 발효시켰다. 발효액의 final pH는 pH $3.9{\pm}0.02$로 유산균의 일반적인 final pH 값과 일치함을 통해 유산균의 발효를 확인하였고, 유산균에 의한 꽃송이버섯 발효의 효과를 ${\beta}$-glucan 함량을 통하여 확인하였다. Yeast Extract broth 발효액은 YSB-2LP 1.65 g/100 g으로 ${\beta}$-glucan을 거의 함유하고 있지 않았지만 MRS broth 발효액은 Yeast Extract broth 발효액의 10배에 달하는 MPB-1LP 10.84 g/100 g을 함유하고 있었다. MPB-1LP는 꽃송이버섯 powder와 L.actobacillus plantarum으로 발효한 발효액으로 pH stress로 인해 만들어진 L. plantarum의 ${\beta}$-D-glucosidase에 의해 분해된 고분자량의 수용성 ${\beta}$-glucan이라 사료된다. 꽃송이버섯을 powder 상태로 L. plantarum과 함께 발효시켰을 때 꽃송이버섯의 수용성 ${\beta}$-glucan 추출 효율을 높일 수 있으며, 본 연구의 결과는 꽃송이버섯 유산균 발효물의 면역촉진 작용 연구를 위한 기초연구자료로 활용될 수 있을 것이다.

• Natural Product Sciences
• /
• 제1권1호
• /
• pp.43-49
• /
• 1995

Two cucurbitane-compounds were isolated from the roots of Bryonia alba L. and the chemical structures were established as 19-norlanost-5-ene-3,1l,22-trione-$2{\beta}$, $16{\alpha}$,$20{\beta}$,25-tetrahydroxy-9-methyl (23,24-dihydrocucurbitacin D) and 2-O-${\alpha}$-D-glucopyranosyl 19-norlanost-5-ene-3,11,22-trione-$2{\beta}$,$16{\alpha}$,$20{\beta}$,25-tetrahydroxy-9-methyl (arvenin IV), respectively, on the basis of chemical and spectral methods. Both of the compounds showed cytotoxic activity against cancer cell lines, A549, SK-MEL-2, COLO 205 and L1210.

• 한국식품과학회지
• /
• 제43권2호
• /
• pp.169-175
• /
• 2011

[ ${\beta}$ ]Xylosidase 효소활성이 높은 균주를 선발하기 위하여 다양한 김치에서 분리된 Leuconostoc 속 젖산균의 ${\beta}$-xylosidase 활성을 탐색하였다. 김치에서 분리된 55개의 Leuconostoc 속 젖산균 중 36개의 균주만이 자일로스를 탄소원으로 이용하였으며, 배추김치에서 분리된 Leu. lactis KCTC 13344 균주가 가장 높은 세포내 ${\beta}$-xylosidase 효소활성을 나타내었으며, 효소활성은 pH 6, $30^{\circ}C$ 반응조건에서 가장 높게 나타났다. $Zn^{2+}$을 제외한 금속이온은 효소활성을 유의적으로 증가시켰으며, $Fe^{2+}$은 1 mM의 농도에서 ${\beta}$-xylosidase 대조구와 비교하여 효소활성을 약 40% 증가시켰다. 균주를 배양할 때 사용한 탄소원 중 자일로스가 가장 높은 효소활성을 나타내었고, 효소활성을 위한 최적의 자일로스 농도는 30 g/L였다. 단백질 전기영동 및 활성염색을 수행한 결과 분자량이 약 64 kDa인 Leu. lactis KCTC 13344 균주의 ${\beta}$-xylosidase는 자일로스에 의하여 발현이 유도되는 것으로 추정되었다. 자일로스가 30 g/L의 농도로 첨가된 MRS 배지에서 Leu. lactis KCTC 13344 균주의 성장은 20시간 후에 최고에 도달하였고, ${\beta}$-xylosidase 효소활성은 16시간 후에 최대 $7.1{\pm}0.3units/mL$이었다. 배양 초기에 주입한 자일로스는 약 20% 정도 소모하였고, 젖산과 아세트산은 3.0 g/L 수준으로 생성되었지만 에탄올은 생성되지 않았다.

• 대한수학회지
• /
• 제38권3호
• /
• pp.503-521
• /
• 2001

A change of Finsler metric L(x,y)longrightarrowL(x,y) is called a Randers change of L, if L(x,y) = L(x,y) +$\rho$(x,y), where $\rho$(x,y) = $\rho$(sub)i(x)y(sup)i is a 1-form on a smooth manifold M(sup)n. Let us consider the special Randers change of Finsler metric LlongrightarrowL = L + $\beta$ by $\beta$. On the basis of this special Randers change, the purpose of the present paper is devoted to studying the conditions for Finsler space F(sup)n which are transformed by a special Randers change of Finsler spaces F(sup)n with ($\alpha$,$\beta$)-metrics of Douglas type to be also of Douglas type, and vice versa.

• 한국환경보건학회지
• /
• 제8권1호
• /
• pp.1-11
• /
• 1982

A study on the water pollution of Gumho river by the relationship between physio-chemical conditions and water quality level by phytoplankton was examined at 7 sampling positions during the period from Aug. 1 to Nov. 30, 1981. Examination of physio-chemicat water analysis such as temperature, pH, DO, BOD, and biological analysis are as follows: 1. pH was in the range of 6.6-7.3. 2. At all positions DO was0.5-11.9 mg/l. But at Shinchun bridge and Gangchang was 0.5-3.9 mg/l. 3. BOD was in the range of 3.4-29.2 mg/l. Banyawol, Dongchon and Gumdan was shown good condition. But at Shinchun bridge was 21.1-29.2 mg/l. 4. The plankton identification in this study period showed, Cyanophyceae is 7 genera 13 species, Bacillariophyceae is 11 genera 32 species, and Chlorophceae is 17 genera 27 species: total 35 genera 72 species. 5. In the point of phytoplankton classification, upper stream of Banyawol, Dongchon and Gumdan which BOD was 3.4-8.7 mg/l, dominant phytoplanktons were Synedra ulna, Ulothrix sp., Oscillatoria sp. and Frusturia rhomboides. At Shinchun bridge which BOD was 21.1-29.2 mg/l, Microcystis aeruginosa, Closterium acerosum and Oscillatoria sp were found a small. At 3rd gongdan which BOD was 9.2-12.5 mg/l, dominant species were Synedra ulna, Hormidium sp and Actinastrum hantzschii. At Paldal which BOD was 7.8-9.2 mg/l, dominant species were Nitzschia palea, Synedra ulna and Scenedesmus bijuga. At Gangchang of down stream which BOD was 6.9-9.2 mg/l, dominant phytoplanktons were Closterium acerosum, Microcystis aeruginosa and Actnastrum hantzschii. 6. The results of biological water analysis by saprobic system were as follows: Banyawol was from oligosaprobic to $\beta$-mesosaprobic, Dongchon and Gumdan was from $\beta$-mesosaprobic to $\beta$-mesosaprobic, Shinchun bridge was polysaprobic, 3rd gongdan was from $\alpha$-mesosaprobic to $\beta$-polysaprobic, Paldal was $\beta$-polysaprobic and Gangchang was $\alpha$-polysaprobic.

• 한국발생생물학회지:발생과생식
• /
• 제22권2호
• /
• pp.155-163
• /
• 2018

This study aimed to investigate changes in the activity and mRNA expression of plasminogen activators (PAs) induced by $17{\beta}$-estradiol ($E_2$), human chorionic gonadotropin (hCG), and interleukin-$1{\beta}$ ($IL-1{\beta}$) in porcine endometrial cells. Endometrial cells were isolated from the epithelium and cultured to 80% confluence. They were then treated for 24 h with $E_2$ (0.2, 2, 20, and 200 ng/mL), $IL-1{\beta}$ (0.1, 1, 10, and 100 ng/mL), and hCG (0.5, 1, 1.5 and 2 IU/mL). mRNA expressions of urokinase-type (uPA) and tissue-type (tPA) PAs were analyzed using reverse transcription PCR, and activities were measured using a PA activity assay. mRNA expressions of uPA and tPA increased with $E_2$ treatment; however, this was not significant. Similarly, treatment with hCG did not influence the mRNA expressions of PAs. Interestingly, treatment with 0.1 ng/mL $IL-1{\beta}$ significantly reduced the mRNA expression of uPA, but did not affect that of tPA. Treatment with 2, 20, and 200 ng/mL $E_2$ increased PA activity compared with the control group; treatment with 0.1 and 1 ng/mL $IL-1{\beta}$ significantly increased PA activity compared with the other $IL-1{\beta}$ treatment groups, whereas treatment with 10 and 100 ng/mL $IL-1{\beta}$ decreased. Treatment with 2 IU/mL hCG increased PA activity compared with the other treatment groups, although there were no significant differences between the hCG and control groups. In conclusion, the activity and mRNA expression of PAs were differently regulated by the hormone/cytokine and its concentration in porcine endometrial cells. Therefore, understanding PA regulatory mechanisms may help to improve the reproductive potential of domestic animals.

• 한국수정란이식학회지
• /
• 제11권2호
• /
• pp.111-124
• /
• 1996

The present study was carried out to investigate the effects of co-culture cells and growth factors on in vitro culture of Korean native cattle(KNC) embryos fertilized in vitro. Two-eight cell embryos were cultured in vitro using 4 types of co-culture cells and 3 growth factors singly or in combination. The results were as follows, In the co-culture of 2~8 cell embryos with bovine oviductal epithelial cell(BOEC), granulosa cell(BGC), uterine epithelial cell(BUEC) and mouse embryonic fibroblast (MEF) monolayers, the developing rate to blastocysts was significantly(P<0.05) higher with BUEC(32.1%) than with MEF(15.3%), BGC(13.2%) and non co-culture control(11.6%). When the morula co-cultured with BOEC for 5 days following in vitro fertilization were co-cultured with BOEC continuously or with BUEC, respectively, the developing rate to blastocysts was higher with BUEC(73.9%) than with BOEC(56.0%). To examine the effects of growth factors on in vitro development of 2~8 cell embryos, epidermal growth factor(EGF), transforming growth factor-$\beta$l(TGF-$\beta$l) and insulin-like growth factor-1(IGF-1) were added singly or in combination to TCM 199 maturation medium with respective concentration. In a addition of each 10, 30 and SOng /rnl EGF, the developing rate to blastocysts was the highest in lOng /ml EGF(25.3%). In addition of each 1, 2 and Sng /mi TGF-$\beta$1, the developing rate to blastocysts was the highest in lng /ml TGF-$\beta$1(28.8%). In addition of each 50, 100ng/ml JGF-l, the developing rate to blastocysts was higher in 100ng/ml IGF-l(16.5%) than in SOng/mi IGF-1(12.9%). When lOng /ml EGF and lng /ml TGF-$\beta$l was added singly or in combination, the developing rate to blastocysts was similar in groups added singly or in combination with EGF and TGF-$\beta$l (23.l~24.6%), although higher than in control(16.7%). In the co-culture of 2~8 cell embryos Wth BOEC + each 10, 30 and 5Ong /rnl EGF, the developing rate to blastocysts was significantly(p<0.05) higher in BOEC + long /ml EGF(32.3%) than in BOEC + 3Ong /ml EGF(18.9%) and BOEC + song /ml EGF(9.7%). In the co-culture of 2~8 cell embryos with BOEC + each 1, 2, Sng /ml TGF-$\beta$l the developing rate to blastocysts was higher in BOEC + Sng/rnl TGF-$\beta$l(28.2%) than in BOEC + lng /ml TGF-$\beta$l(21.7%) and BOEC + 2ng/ml TGF-$\beta$l(21.4%). In summary, higher developing rate to blastocysts were obtained with co-culture of BUEC for co-culture system, with addition of lOng /ml EGF or lng /ml TGF-$\beta$l for growth factor culture system, and with co-culture of BOEC + lOng /ml EGF or BOEC + Sng /ml TGF-$\beta$l for co-culture + growth factor culture system.

• 생약학회지
• /
• 제44권1호
• /
• pp.16-21
• /
• 2013

The fruits of Pourthiaea villosa were extracted with methanol and its extract was fractionated with n-hexane, methylene chloride, ethyl acetate and n-butanol. Repeated column chromatography of silica gel, sephadex LH-20 and HPLC led to the isolation of nine phenolic compounds from ethyl acetate soluble fraction. The chemical structures were elucidated as kaemferol-3-O-${\beta}$-D-glucopyranoside (astragalin) (1), isorhamnetin-3-O-${\beta}$-D-glucopyranoside (2), kaempferol-3-O-${\beta}$-D-xylopyranosyl($1{\rightarrow}2$)-${\alpha}$-L-rhamnopyranoside (3), caffeic acid (4), quercetin-3-O-${\beta}$-D-xylopyranosyl($1{\rightarrow}2$)-a-L-rhamnopyranoside (5), quercetin-3-O-${\beta}$-D-xylopyranosyl($1{\rightarrow}2$)-${\beta}$-D-glucopyranoside (6), quercetin-3-O-${\beta}$-D-xylopyranosyl($1{\rightarrow}2$)-${\beta}$-D-galactopyranoside (7), quercetin-3-O-${\alpha}$-L-rhamnopyranoside (quercitrin) (8), and kaempferol-3-O-${\alpha}$-L-rhamnopyranoside (afzelin) (9) by spectroscopic techniques. These compounds were isolated from this plant for the first time.

• 한국식품영양과학회지
• /
• 제39권1호
• /
• pp.31-35
• /
• 2010

본 실험에서는 hamster $\beta$-cell인 HIT-T15 cell을 이용하여 돼지감자추출물의 생리활성 및 기능을 검증하고자 하였다. 돼지감자추출물을 첨가한 NC(0 ${\muL/mL$), HT2(1.1 ${\muL/mL$), HT3(1.5 ${\muL/mL$)군과 inulin을 첨가한 NC(0 ${\muL/mL$), IN2(1.8 ${\muL/mL$), IN3(2.5 ${\muL/mL$)군으로 나누어 실험하였다. 세포 viability 측정한 결과 시료를 첨가하지 않은 군을 100%로 보았을 때 돼지감자추출물을 첨가한 HT3(1.5 ${\muL/mL$)군과 inulin을 첨가한 IN2(1.8 ${\muL/mL$), IN3(2.5 ${\muL/mL$) 군에서 세포생존율이 유의적으로 증가하였다(p<0.05). 시료처리 후 췌장 $\beta$-세포 파괴를 유도하지 않고 HIT-T15 cell의 cell culture supernatant를 이용하여 cytotoxicity를 측정한 결과 시료를 첨가하지 않은 NC(0${\muL/mL$)군에 비해 모든 군에서 cytotoxicity가 낮게 나타났다. Alloxan(4 mM)으로 $\beta$-세포 파괴를 유도하여 HIT-T15 cell에서 세포보호 효과를 측정한 결과 시료를 첨가하지 않은 NC(0 ${\muL/mL$)군에 비해 돼지감자추출물을 첨가한 HT2(1.1 ${\muL/mL$), HT3(1.5 ${\muL/mL$)군에서 세포생존율이 유의적으로 증가하였다(p<0.05). 또한 췌장 $\beta$-세포 파괴를 유도하여 HIT-T15 cell이 분비한 인슐린 분비능 및 세포 내 $NAD^+$/NADH 함량을 측정한 결과 시료를 첨가하지 않은 NC(0 ${\muL/mL$)군에 비해 돼지감자추출물을 첨가한 HT3(1.5 ${\muL/mL$)군에서 인슐린 분비량과 $NAD^+$/NADH 함량이 유의적으로 증가하였다(p<0.05). 이상의 연구 결과 돼지감자추출물은 HIT-T15 cell의 생존율을 높이고, 세포보호 효과를 가짐으로써 인슐린 분비능 정상화 및 $NAD^+$ 함량을 증가시켜 혈당 조절 및 당뇨에 긍정적 효과가 있을 것으로 사료된다.

• 약학회지
• /
• 제47권6호
• /
• pp.450-455
• /
• 2003

Synthesis of (lR,5S,6S)-6-[(lR)-1-hydroxyethyl] -2-[(3S,5S)-5-(2-ethoxycarbonyl-1-moxy(hydroxy)iminoethyl)pyrrolidine-3-ylthio]-1-methylcarbapen-2-em-3-carboxylic acids (10a,l0b) were described. Methyl(2S,4S)-4-tritylthio-1-(allyloxycarbonyl)pyrrolidine-2-carboxyla late (I) was prepared from trans-4-hydroxy-L-proline with (2S,4R)-abs olute configuration as starting material. (2S,4S)-1-allyloxycarbonyl-2-(2-ethoxycarbonyl-hydroxy(methoxy )iminoethyl)-4-mercapto- pyrrolidines (6,7) were obtained from the tritylthio compound (I). (lR,5S,6S)-6-[(lR)-1-hydroxyethyl]-2-[(3S,5S)-5-(2-ethoxycarbonyl-1-methoxy(hydroxy)imino-ethyl)pyrrolidine-3-ylthio]-1-methylcarbapem-2-em-3-carboxylic acids (10a,10b) were obtained by the coupling reaction with carbapenem diphenylphosphates (8) and pyrrolidine-thiol moiety (6,7). Their in vitro antibacterial activities against both Gram-positive and Gram-negative were tested. Compounds ( 10a,10b) showed potent antibacterial activity except pseudomonas aerusinosa.