• 제목/요약/키워드: gas chromatography/mass spectrometry identification

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사과 성숙(成熟) 및 저장중(貯藏中) 향기성분(香氣成分)의 변화(變化) -제일보(第一報). 과실(果實) 성숙중(成熟中) 향기성분(香氣成分)의 동정(同定) 및 정량(定量)- (Changes of Volatiles from Apple Fruits during Maturity and Storage -Part. I. Identification and Determination of Volatiles in the Fruits-)

  • 심기환;손태화;김명찬;강신권;박석규
    • Applied Biological Chemistry
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    • 제27권1호
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    • pp.14-20
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    • 1984
  • 우리 나라에서 비교적 생산량이 많은 사과과실 3품종(Fuji, 홍옥, 국광)을 대상으로 향기성분을 분리 및 동정하고, 또한 성숙시기별로 향기성분의 함량변화를 측정하였다. 향기성분은 30종 이상 분리되었고 그 중 ester 23종, alcohol 9종 및 aldehyde 2종을 동정하였다. 성숙중 향기성분의 종류와 함량은 증가하였으며 1-butanol, isobutyl butyrate, 2-pentanol, ethyl valerate 및 hexanal 등의 함량이 많았다.

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압출성형에 의해 제조된 구운 쇠고기 반응향의 특징적인 향기성분 동정 (Identification of Characteristic Aroma-active Compounds from Burnt Beef Reaction Flavor Manufactured by Extrusion)

  • 김기원;서원호;백형희
    • 한국식품과학회지
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    • 제38권5호
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    • pp.621-627
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    • 2006
  • 압출성형에 의해 제조된 구운 쇠고기 반응향의 향특성을 알아보기 위해 휘발성 성분 및 aroma-active화합물을 SDE-GC-MS-O법을 이용하여 분석하였다. HVP에 ribose, cysteine, furaneol, thiamin, methionine, 마늘 분말 및 인지질 등의 전구문질을 넣고 최적 압출성형 조건인 $160^{\circ}C$, 스크루 속도 45 rpm 및 윈료공급 속도 38 kg/hr에서 압출성형하였다. 압출성형에 의해 제조된 구운 쇠고기 반응향에서 모두 68개 의 휘발성 성분이 검출되었으며, 그 숫자는 furaneol을 빼고 압출성형 시킨 반응향과 HVP만 압출성형 시킨 시료에서 크게 줄어들었다. GC-O결과 구운 쇠고기 반응향에서 27개의 aroma-active 화합물이 검출되었으며, methional과 2-methyl-3-furanthiol이 가장 중요한 aroma-active화합물로 밝혀졌다. Furaneol이 구운 쇠고기 반응향 생성에 있어서 중요한 역할을 할 것으로 생각되어 진다.

금강 수계 주요지류인 갑천과 미호천에서 잠정유해물질 오염원 확인 연구 (Contamination Sources of Several Potentially Hazardous Compounds Found at the Gap Stream and the Miho Stream, Two Major Tributaries of the Geum River)

  • 이준배;이재정;조윤해;윤조희;홍선화;이대희;이수형;조영환;신호상
    • 한국환경농학회지
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    • 제35권1호
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    • pp.15-23
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    • 2016
  • BACKGROUND: Water quality is of concern to water utility operators, public health officials, and populations using the water. If any contaminant is released from a point of entry, it could be spread rapidly throughout the water stream. So the identification of the location of the points of entry and its release history are critical informations to establish the management strategy.METHODS AND RESULTS: Aniline, nonylphenol, pentachlorophenol and formaldehyde in 39 surface water samples were analysed using Gas chromatography-mass spectrometry (GC-MS) methods. Formaldehyde, aniline and nonylphenol were mainly detected in the near sites where industrial waste water and domestic sewage were discharged into stream. But pentachlorophenol was detected in the downstream samples where pulp manufacturing plants were operated.CONCLUSION: Results indicate that pentachlorophenol found in main stream of Guem river was mainly introduced from pulp manufacture industries. Otherwise, formaldehyde, aniline and nonylphenol were mainly contaminated from the industrial waste water and domestic sewage.

업종별 유해성 유기물질의 확인에 대한 연구 (A Study on the Identification of Hazardous Organic Substances for Industrial Classification)

  • 박선구;김성수;고오석;정성웅;박준대;유승도;류재근;조현우
    • 분석과학
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    • 제9권4호
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    • pp.392-398
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    • 1996
  • 광주천 유역내에 분포된 8개 업종 26개 배출원의 원폐수로부터 인간에게 유해한 11개의 유기화학물질 tetrachloroethylene, ethyl benzene, p-xylene, o-xylene, isopropyl benzene, n-propyl benzene, 1,2,4-trimethyl benzene, 1,3,5-trimethyl benzene, p-isopropyl toluene, see-butyl benzene, naphthalene을 액체-액체 추출법으로 분리하였다. 추출물 중 각 화합물들의 구조는 기체 크로마토그래피/질량분석계(GC/MS)를 사용하여 확인하였고, 표준시료와 비교함으로써 밝혔다.

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Allelopathy 작용성(作用性)을 나타내는 잡초(雜草)중의 휘발성(揮發性) Terpene류(類)의 동정(同定) (An Identification of Volatile Terpenes in Allelopathic Weeds)

  • 전재철;한강완
    • 한국잡초학회지
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    • 제9권2호
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    • pp.149-153
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    • 1989
  • Allelopathy 작용성(作用性)을 나타내는 4종(種)의 잡초(雜草) 중에 존재(存在)하는 휘발성(揮發性) terpene 물질(物質)을 GC 및 GC-MS로 동정(同定)하였다. 쑥에서는 26종(種)의 휘발성(揮發性) terpene 류(類)를 분리(分離) 동정(同定)하였는데 이들은 monoterpene 16종(種)과 sesquiterpene 10종(種)이었다. 또한 토끼풀에서는 4종(種), 쇠비름과 냉이에서 각(各) 3종(種)이 확인(確認)되었다. 동정(同定)된 terpene 중 allelopathy 작용성(作用性)을 나타내는 물질(物質)로는 쑥에서 ${\alpha}$-phellandrene, 1,8-cineole, limonene, ${\beta}$-pinene, borneol, selinene 및 caryophyllene, 토끼풀에서 ${\alpha}$-pinene과 ${\beta}$-caryophyllene, 그리고 냉이에서 ${\alpha}$-pinene 등이었고, 쇠비름 중에는 allelopathy 작용성(作用性)을 나타내는 휘발성(揮發性) terpene 류(類)는 없는 것으로 나타났다.

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더위지기 정유로부터 아세틸콜린에스테라제 억제활성 성분의 동정 (Identification of the Component with Anti-acetylcholinesterase Activity from the Essential Oil of Artemisia iwayomogi)

  • 최재수;송병민;박희준
    • 한국자원식물학회지
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    • 제30권1호
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    • pp.17-21
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    • 2017
  • AChE 억제제는 알츠하이머 질환 치료에 이용될 수 있으므로, 본 연구는 더위지기 정유로부터 AChE 활성성분을 탐색하기 위하여 수행한 것이다. 더위지기로부터 얻은 정유를 GC-MS로 분석했을 때 camphor가 29.8%, borneol이 28.0%, eucalyptol이 5.81%, coumarin이 5.49%의 피크 면적 비율을 보였다. 이 중 camphor, borneol, coumarin을 사용하여 Anti-AChE 활성 검색을 수행하였다. 그 결과, $0.298mg/m{\ell}$, coumarin은 $0.236mg/m{\ell}$$IC_{50}$ 값을 나타내었다. 이러한 결과는 coumarin이 anti-AChE 활성을 나타내는 활성물질임을 나타내는 것이다.

가스크로마토그라피/질량분석기에 의한 모발중 대마성분 분석 (Analysis of $\triangle^9$-Tetrahydrocannabinol and 11-nor-9-carboxytetrahydrocannabinol in Hair by Gas Chromatography/Mass Spectrometry)

  • 양원경;한은영;박용훈;임미애;정희선
    • 약학회지
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    • 제48권3호
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    • pp.207-212
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    • 2004
  • An analytic method was developed for the quantitation of $\Delta$$^{9}-$ tetrahydrocannabinol (THC) and 11-nor-9-carboxy THC (THC-COOH) in human hair. After hair samples were pulverized using Freezer Mill, deuterated internal standards were added and digested in 1 N NaOH at $100^{\circ}C$ water bath for 30 min. Digest solutions were extracted by 5 ml hexane:ethyl acetate (90:10) after acidification with acetic acid. The organic phase was evaporated under N 2 and derivatized by BSTFA (with 1% TMCS) at $85^{\circ}C$ for 45 min. The derivatized solution was separated on HP-5MS column ($30m{\times}0.25mm{\times}0.25mm$) and detected using EI-GC-MS with selective ion monitoring mode. The assay of calibration was ranged from 5 to 100 ng/50 mg hair ($r^2$>0.99) for THC and THC-COOH. Within and between-run precision were calculated at 6, 30, 60 ng/50 mg hair with coefficients of variation less than 11%. Within and between run accuracies at the same concentrations were$\pm$14% and $\pm$30% of target for both analytes, respectively. Absolute and relative recovery at 10 and 100 ng were 60∼91%. The method was used to detect and quantify THC and THC-COOH in cannabis abuser's hairs (N = 16) and SRM (N=5, THC 1 ng/mg, NIST). We detected THC and THC-COOH in only one hair sample. In SRM, % accuracy was 93% (range 86∼103%) and precision (% CV) was 8.14. We began to set up a quantitative analysis of THC and THC-COOH using EI-GC-MS. Continuously, we need to modify and develop this method in order to apply for identification in cannanbis users' hair.

geoA 유전자를 이용한 사상형 남조류(Nostocales, Oscillatoriales)의 Geosmin 생성능 검출 (Detection of Geosmin Production Capability Using geoA Gene in Filamentous Cyanobacteria (Nostocales, Oscillatoriales) Strains)

  • 류희성;신라영;서경애;이정호;김경현
    • 한국물환경학회지
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    • 제34권6호
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    • pp.661-668
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    • 2018
  • Geosmin is volatile metabolites produced by a range of filamentous cyanobacteria which causes taste and odor problems in drinking water. Molecular ecological methods which target biosynthetic genes (geoA) are widely adopted to detect geosmin-producing cyanobacteria. The aim of this study was to investigate the potential production capability of 8 strains isolated from the Nakdong River. Ultimately, a suggestion for a genetical monitoring tool for the identification of geosmin producers in domestic waters was to be made. Geosmin was detected using solid phase microextraction gas chromatography mass spectrometry (SPME GC-MS) in two strains of Dolichospermum plactonicum (DGUC006, DGUC012) that were cultured for 28 day. The highest concentrations during the experiment period was $17,535ngL^{-1}$ and $14,311ngL^{-1}$ respectively. Additionally, geoA genes were amplified using two primers (geo78F/971R and geo78F/982R) from strains shown to produce geosmin, while amplification products were not detected in any of non-producing strains. PCR product (766 bp) was slightly shorter than the expected size for geosmin producers. According to the BLAST analysis, amplified genes were at nucleotide level with Anabaena ucrainica (HQ404996, HQ404997), Dolichospermum planctonicum (KM13400) and Dolichospermum ucrainicum (MF996872) between 99 ~ 100 %. Both strains were thus confirmed as potential geosmin-producing species. We concluded that the molecular method of analysis was a useful tool for monitoring potential cyanobacterial producers of geosmin.

Analysis of the essential oil composition of fresh Panax ginseng root and identification of novel phenylalkenal compounds

  • Dae-Woon Kim;Young-Hoi Kim;Tae-Young Kim;Han-Suk Choi;Myung-Kon Kim
    • 한국식품저장유통학회지
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    • 제30권6호
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    • pp.944-959
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    • 2023
  • This study investigated the essential oil composition of fresh Panax ginseng root and identified novel compounds from ginseng oil. The oil was divided into five fractions (neutral, basic, phenolic, acidic, and aldehydic). In total, 149 constituents, including 29, 19, and 38 compounds in the basic, phenolic, and aldehydic fractions, respectively, were identified by gas chromatography (GC) and GC-mass spectrometry (MS). The primary constituents of the total ginseng volatile oil were α-humulene (13.91% as a peak area), bicyclogermacrene (13.59%), β-caryophyllene (8.24%), α-neoclovene (7.78%), and α- and β-panasinsenes (5.14% and 7.53%). The primary constituents of the basic fraction were 2-isopropyl-3-methoxypyrazine (35.51%), 3-sec-butyl-2-methoxy-5-methylpyrazine (31.54%), 2-isobutyl-3-methoxypyrazine (8.64%), and 2-methoxy-3-methylpyrazine (8.40%), whereas in the phenolic fraction, these were benzoic (25.40%), octanoic (11.57%), nonanoic (9.16%), propionic (6.35%), and decanoic acids (6.16%). The primary constituents of the aldehydic fraction were 4-(2-furyl)-3-buten-2-one (23.41%), benzaldehyde (10.18%), cis-2-heptanal (9.42%), 3-(α-furyl)-propenal (8.51%), and 2-phenyl-2-butenal (7.28%). Among these, the phenylalkenal compounds, including 2-phenyl-2-butenal, 2-methyl-3-phenyl-2-propenal, 5-methyl-2-phenyl-2-pentenal, 5-methyl-2-phenyl-2-hexenals, 2-phenyl-2-octenal, and 2-phenyl-2-nonenal, were newly identified in this study as ginseng volatile constituents. Furthermore, 2-phenyl-2-nonenal was identified as a plant-based volatile constituent for the first time in this study.

Glycosyl glycerides from hydroponic Panax ginseng inhibited NO production in lipopolysaccharide-stimulated RAW264.7 cells

  • Cha, Byeong-Ju;Park, Ji-Hae;Shrestha, Sabina;Baek, Nam-In;Lee, Sang Min;Lee, Tae Hoon;Kim, Jiyoung;Kim, Geum-Soog;Kim, Seung-Yu;Lee, Dae-Young
    • Journal of Ginseng Research
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    • 제39권2호
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    • pp.162-168
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    • 2015
  • Background: Although the aerial parts of hydroponic Panax ginseng are reported to contain higher contents of total ginsenosides than those of roots, the isolation and identification of active metabolites from the aerial parts of hydroponic P. ginseng have not been carried out so far. Methods: The aerial parts of hydroponic P. ginseng were applied on repeated silica gel and octadecylsilane columns to yield four glycosyl glycerides (Compounds 1-4), which were identified based on nuclear magnetic resonance, infrared, fast atom bombardment mass spectrometry, and gas chromatography/mass spectrometry data. Compounds 1-4 were evaluated for inhibition activity on NO production in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Results and conclusion: The glycosyl glycerides were identified to be (2S)-1-O-7(Z),10(Z),13(Z)-hexadecatrienoyl-3-O-${\beta}$-$\small{D}$-galactopyranosyl-sn-glycerol (1), (2S)-1-O-linolenoyl-3-O-${\beta}$-$\small{D}$-galactopyranosyl-sn-glycerol (2), (2S)-1-O-linolenoyl-2-O-linolenoyl-3-O-${\beta}$-$\small{D}$-galactopyranosyl-sn-glycerol (3), and 2(S)-1-O-linoleoyl-2-O-linoleoyl-3-O-${\beta}$-$\small{D}$-galactopyranosyl-sn-glycerol (4). Compounds 1 and 2 showed moderate inhibition activity on NO production in LPS-stimulated RAW264.7 cells [half maximal inhibitory concentration ($IC_{50}$): $63.8{\pm}6.4{\mu}M$ and $59.4{\pm}6.8{\mu}M$, respectively] without cytotoxicity at concentrations < $100{\mu}M$, whereas Compounds 3 and 4 showed good inhibition effect ($IC_{50}$: $7.7{\pm}0.6{\mu}M$ and $8.0{\pm}0.9{\mu}M$, respectively) without cytotoxicity at concentrations < $20{\mu}M$. All isolated compounds showed reduced messenger RNA (mRNA) expression of interleukin-$1{\beta}$ (IL-$1{\beta}$), IL-6, and tumor necrosis factor-${\alpha}$ in LPS-induced macrophage cells with strong inhibition of mRNA activity observed for Compounds 3 and 4.