• 식물조직배양학회지
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• 제21권2호
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• pp.111-115
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• 1994

벼(Oryza sativa L. cv Nipponbaie)배양세포에 중력 450,000 x g를 처리하여 cDNA library를 만들고, 무처리 및 고중력을 처리한 cDNA 프로브로 스크리닝을 실시하여 고중력에 특이적으로 양성반응을 나타내는 GSC 13 및 GSC124 cDNA를 선발하였다. 선발된 두 유전자 GSC 13 및 GSC 124의 길이는 각각 1.34 및 0.67 kilobase pairs였으며, 배양세포내에서 관련된 transcript의 크기는 각각 2.0 및 1.9 kilobase pairs인 것으로 나타났다. 두 유전자를 프로브로한 Northern hybridization을 실시한 결과 GSC 13, GSC 124 공히 배양세포내에 고중력처리에 의해 특이적으로 축적되는 mRNA가 나타났으며, 중력강도 300,000 x g 에 비해 450,000 x g 처리에서 더욱 강한 축적을 보였고 450,000 x g 4시간 처리에서 최대의 수준을 보였다.

• 한국환경농학회지
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• 제18권2호
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• pp.126-134
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• 1999

낙동강 수계 농업용수의 수질개선 및 수자원관리를 위한 기초자료를 얻기 위하여 낙동강 본류 4개지점과 지류 3개지점의 수질을 1995년 1월부터 1997년 11월까지 매월 1회 총 36회에 걸쳐 수질특성을 조사한 결과는 다음과 같다. 수온은 본류와 지류의 각 지점별 수온차는 거의 없었으며 동절기는 평균수온이 $5^{\circ}C$이하이고 하절기는 $26^{\circ}C$이상으로 큰 차이를 보였고, 낙동강 본류의 지점별 pH는 $6.3{\sim}9.3$ 범위로서 적포지역과 남지지역은 봄과 가을에 pH8.5 이상으로 대부분 농업용수 허용기준치인 pH $6.0{\sim}8.5$를 초과하였으며, 낙동강 지류의 지점별 pH는 $6.5{\sim}8.5$ 범위였다. 각 지점별 DO는 금호강 하류인 강창지점을 제외하고는 대부분 $8.0{\sim}13mg/l$ 정도의 분포를 나타내었고, BOD는 금호강이 합류되기 전인 다사지점은 $1.5{\sim}4.8mg/l$로서 농업용수 허용기준치인 8mg/l 이하였으나 금호강이 합류된 후인 고령은 $3.8{\sim}8.9mg/l$, 적포는 $3.4{\sim}8.4mg/l$ 그리고 남지는 $3.3{\sim}7.8mg/l$로서 이들 지점은 시기에 따라서 농업용수허용 기준치를 초과하는 경우가 많았다. 특히 낙동강 지류인 금호강 강창지점의 BOD는 $7.6{\sim}18.5mg/l$로서 금호강은 낙동강의 주된 오염원인 것으로 나타났다. COD는 본류의 경우 고령이 $5.2{\sim}13.5mg/l$, 적포의 경우 $5.0{\sim}12.7mg/l$ 그리고 남지는 $5.0{\sim}12.2mg/l$의 범위로서 시기에 따라서 농업용수허용기준치인 8mg/l을 초과하는 경우가 많았으며, COD값은 BOD값에 비하여 훨씬 높게 나타났으며 하류지역으로 갈수록 그 농도차의 폭이 컸다. $NH_4-N$은 본류의 경우 금호강($0.5{\sim}13.1mg/l$)의 영향을 크게 받는 고령지점이 $0.18{\sim}5.0mg/l$로서 가장 높았고, 적포는 $0.03{\sim}4.49mg/l$, 남지는 $0.01{\sim}3.81mg/l$ 범위였으며, 여름철에 비하여 갈수기인 겨울철에 $NH_4-N$가 매우 높게 검출되었다. T-N은 금호강의 영향을 크게 받는 고령이 $4.96{\sim}12.06mg/l$ 범위로서 가장 높았으며, 다사지점 $2.86{\sim}4.86mg/l$, 적포지점 $4.20{\sim}8.20mg/l$, 남지지점 $3.18{\sim}8.64mg/l$로서 대부분이 농업용수기준치인 1.0mg/l을 훨씬 초과하였다. T-P도 고령이 $0.10{\sim}0.58mg/l$ 범위로서 가장 높았으며, 적포지점 $0.07{\sim}0.36mg/l$, 남지지점 $0.08{\sim}0.41mg/l$로서 대부분이 농업용수기준치인 0.1mg/l을 초과하였으며, 낙동강 수계의 T-N 및 T-P 농도는 매년 증가하는 경향이었다. 중금속은 Cu가 $ND{\sim}0.047mg/l$, Zn는 $ND{\sim}0.041mg/l$ 범위의 농도로 검출되었고 Cd, Pb, Cr, Hg 및 As는 검출되지 않았다.

• Mycobiology
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• 제51권3호
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• pp.148-156
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• 2023

Penicillium oxalicum strain can be isolated from the Bletilla striata (Thunb.) Reichb. f. tubers. Its solid-state fermentation products are concentrated by percolation extraction. Separation and purification have been conducted to the ethyl acetate extracts by preparative HPLC. Based on the use of spectrometry, we have determined 17 known compounds, 12,13-dihydroxy-fumitremorgin C (1), pseurotin A (2), tyrosol (3), cyclo-(L-Pro-L-Val) (4), cis-4-hydroxy-8-O-methylmellein (5), uracil (6), cyclo-(L-Pro-L-Ala) (7), 1,2,3,4-tetrahydro-4-hydroxy-4-quinolin carboxylic acid (8), cyclo-(Gly-L-Pro) (9), 2'-deoxyuridine (10), 1-(b-D-ribofuranosyl)thymine (11), cyclo-(L-Val-Gly) (12), 2'-deoxythymidine (13), cyclo-(Gly-D-Phe) (14), cyclo-L-(4-hydroxyprolinyl)-D-leucine (15), cyclo-(L)-4-hydroxy-Pro-(L)-Phe (16), uridine (17). Here, we report compounds 1-3, 5, 7-8, 11-12, 14-17 are first found and isolated from this endophyte.

• Natural Product Sciences
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• 제22권2호
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• pp.93-101
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• 2016

For efficient quality control of the Samryeongbaekchul-san decoction, a powerful and accurate an ultra-performance liquid chromatography (UPLC) coupled with electrospray ionization (ESI) tandem mass spectrometry (MS) method was developed for quantitative analysis of the thirteen constituents: allantoin (1), spinosin (2), liquiritin (3), ginsenoside Rg1 (4), liquiritigenin (5), platycodin D2 (6), platycodin D (7), ginsenoside Rb1 (8), glycyrrhizin (9), 6-gingerol (10), atractylenolide III (11), atractylenolide II (12), and atractylenolide I (13). Separation of the compounds 1 - 13 was performed on a UPLC BEH $C_{18}$ column ($2.1{\times}100mm$, $1.7{\mu}m$) at a column temperature of $40^{\circ}C$ with a gradient solvent system of 0.1% (v/v) formic acid aqueous-acetonitrile. The flow rate and injection volume were 0.3 mL/min and $2.0{\mu}L$. Calibration curves of all compounds were showed good linearity with values of the correlation coefficient ${\geq}0.9920$ within the test ranges. The values of limits of detection and quantification for all analytes were 0.04 - 4.53 ng/mL and 0.13 - 13.60 ng/mL. The result of an experiment, compounds 2, 6, 12, and 13 were not detected while compounds 1, 3 - 5, and 7 - 11 were detected with 1,570.42, 5,239.85, 299.35, 318.88, 562.27, 340.87, 12,253.69, 73.80, and $115.01{\mu}g/g$, respectively.

• Advances in environmental research
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• 제6권3호
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• pp.217-227
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• 2017

In this study, the elimination of $Ni^{2+}$ using 13X sorbent due to an electrostatic interaction was reported. The significant factors including pH, time and 13X sorbent amount were investigated using Box-Behnken design (BBD). In the optimum experimental conditions, the linear rang and limit of detection of the proposed method were 0.1-20 and $0.102mg\;L^{-1}$, respectively. The precision as RSD% was 1.3% for concentration of $2mg\;L^{-1}$. Concerning the excellent recoveries in a short time with highly efficient sample clean-up and removal, this method may be a very powerful and innovative future sample removal technique. To the best of our knowledge, this is the first report on using BBD for optimizing the parameters affected the removal of $Ni^{2+}$ by 13X zeolite sorbent.

• Preventive Nutrition and Food Science
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• 제13권2호
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• pp.66-70
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• 2008

In order to develop a functionally improved kochujang with antiobesity effects, garlic-added kochujang was prepared with freeze-dried garlic powder and followed by fermentation for 60 days at $30^{\circ}C$. Antiobesity effect of the garlic-added kochujang was investigated by measuring the leptin secretions and mRNA expression levels of obesity-related gene such as TNF${\alpha}$, PPAR${\gamma}$, C/EBP${\alpha}$, and SREBP1c, in cultured 3T3-L1 adipocytes. Fermentation of garlic-added kochujang led to decreased levels of leptin secretions and reduced the mRNA expression levels of TNF${\alpha}$, PPAR${\gamma}$, C/EBP${\alpha}$, and SREBP1c in the 3T3-L1 adipocytes. Accordingly, these results suggest that the addition of garlic to kochujang has a potential as a valuable functional food for controlling obesity.

• 대한화학회지
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• 제38권11호
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• pp.808-818
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• 1994

$MCl_z$(M = Mo; z = 5, M = V; z = 3)과 N,P 주개 리간드를 acetonitrile 용매에서 반응시켜 중성착물 [$MCl_3L_2$(MeCN)] (M = Mo, V: L = $PPh_3$, 1/2 phda)을 합성하였다. Acetone 용액에서 이들 중성 화합물과 $AgClO_4$를 반응시켜 [$MCl_3-_nL_2(MeCN)(S)_n$]$(ClO_4)_n$ (n = 1, 2 : s = solvent)의 양이온 화합물을 얻었다. 2가의 양이온 화합물과 중성 화합물을 반응시켜 염소가 다리 연결된 이핵 화합물 $[(MeCN)(L)_2ClM({\mu}-Cl)_2M'Cl(L)_2(MeCN)](ClO_4)_2$ 및 1가의 양이온 화합물과 pyzidine을 2:1 화학양론으로 반응시켜 pyzidine이 다리 결합된 이핵 화합물 $[(MeCN)(L)_2Cl_2M({\mu}-pyz)M'Cl_2(L)_2(MeCN)](ClO_4)_2$형의 호모(M = M'), 헤테로(M ${\neq}$ M') 화합물을 합성하였다. 합성한 착물들은 원소분석과 적외선, $^1H$, $^{13}C$ 핵자기 공명 및 전자 흡수스펙트럼 등을 이용하여 그 특성을 조사하였다.

• Preventive Nutrition and Food Science
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• 제13권2호
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• pp.122-127
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• 2008

The aroma constituents of Chrysanthemum indicum L. were separated by the hydro distillation extraction method using a Clevenger-type apparatus, and were analyzed by gas chromatography-mass spectrometry (GC/MS). The yield of Chrysanthemum indicum L. flower oil was 2.0% (w/w) and the color was light golden yellow. Sixty-three volatile flavor components, which make up 89.28% of the total aroma composition of the flower oil, were tentatively characterized. This essential oil contained 35 hydrocarbons (48.75%), 12 alcohols (19.92%), 6 ketones (15.31%), 3 esters (4.61%), 5 aldehydes (0.43%), 1 oxide (0.22%), and 1 miscellaneous component (0.04%). ${\alpha}$-Pinene (14.63%), 1,8-cineol (10.71%) and chrysanthenone (10.01%) were the predominant volatile components in Chrysanthemum indicum L., an aromatic medicinal herbaceous plant.

• 대한화학회지
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• 제38권10호
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• pp.749-752
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• 1994

하와이 Pohnpei에서 채집한 soft coral Sinularia lochmodes로부터 2개의 furanosesquiterpenes인 (5'E)-5-(2',6'-dimethylocta-5',7'-dienyl) furan-3-carboxylic acid (1)와 (1'E,5'E)-5-(2',6'-dimethylocta-l',5',7'-trienyl) furan-3-carboxylic acid (2)가 검출되었다. 이들의 구조를 $^1H$ , $^{13}C$ NMR, Homo-COSY, $^1H$-$^{13}C$ (1 bond) Heteronuclear Multiple Quantum Coherence Spectroscopy (HMQC), $^1H$-$^{13}C$ (2 and 3 bond) Heteronuclear Multiple Bond Coherence Spectroscopy (HMBC), Electron Impact Mass Spectroscopy (EI-ms) 및 Infrared Spectroscopy (IR)에 의해 밝혔다.

• Bulletin of the Korean Chemical Society
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• 제32권8호
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• pp.2565-2570
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• 2011

The reaction of bromoacetonitrile with 3,14-dimethyl-2,6,13,17-tetraazatetracyclo[$16.4.1^{2.6}.0^{1.18}.0^{7.12}$]tricosane ($L^{10}$) containing a N-$CH_2$-N linkage produces 17-cyanomethyl-3,14-dimethyl-2,6,13,17-tetraazatetracyclo-[$16.4.1^{2.6}.0^{1.18}.0^{7.12}$]tricosane ($L^{11}$). The mono-N-functionalized macrocyclic complexes $[ML^2]^{2+}$ (M = Ni(II) or Cu(II); $L^2$ = 2-cyanomethyl-5,16-dimethyl-2,6,13,17-tetraazatricyclo[$16.4.0.0^{7.12}$]docosane) can be prepared by the reaction of $L^{11}$ with nickel(II) or copper(II) ion in acetonitrile. The N-$CH_2CN$ group attached to $[ML^2]^{2+}$ readily reacts with water or methanol to yield the corresponding complexes of $HL^3$ bearing one N-$CH_2CONH_2$ pendant arm or $L^4$ bearing one $N-CH_2C(=NH)OCH_3$ group. The $N-CH_2CONH_2$ or $N-CH_2C(=NH)OCH_3$ group of each complex is coordinated to the central metal ion. Both $[NiL^4(H_2O)]^{2+}$ and $[CuL^4]^{2+}$ are quite stable in acidic aqueous solutions, but undergo hydrolysis to yield $[Ni(HL^3)(H_2O)]^{2+}$ or $[Cu(HL^3)]^{2+}$ in basic aqueous solutions. In contrast to $[Cu(HL^3)]^{2+}$, $[Ni(HL^3) (H_2O)]^{2+}$ is readily deprotonated to form $[NiL^3 (H_2O)]^+$ ($L^3$ = a deprotonated form of $HL^3$) in basic aqueous solutions.