• Journal of Ginseng Research
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• 제21권3호
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• pp.196-200
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• 1997

The headspace volatiles of the Korean ginseng and the Chinese ginseng were extracted using the SepPak Cl8 cartridge (Wasters Co.) and were analyzed using GC/MSD. The overall GC pattern of the headspace volatiles of the Chinese ginseng was similar to that of the Korean ginseng, but the composition ratios of the two major components, $\beta$-panasinsene to $\beta$-muurolene, were quite different between them. The composition ratios of $\beta$-panasinsene to $\beta$-muurolene of the Korean red and white ginseng were 1.02$\pm$0.28 (n=19) and 1.49$\pm$0.55 (n=14) , respectively. However the com- position ratios of the Chinese red and dried ginseng were 0.58$\pm$0.19 (n=41) and 0.57$\pm$0.17 (n=28), repetitively, which were significantly lower than those of the Korean ginseng at I% level. The composition ratio of the two major headspace volatile components, $\beta$-panasinsene to ${\gamma}$-muurolene, is thought to be as a useful indicator for differentiating the Chinese ginseng with the Korean ginseng.

• 한국식품영양학회지
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• 제32권4호
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• pp.284-293
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• 2019

This study investigated the volatile flavor composition of essential oils from Ligularia fischeri and Ligularia fischeri var. spiciformis. The essential oils obtained from the plants were analyzed by gas chromatography (GC) and GC-mass spectrometry (GC-MS). 99.63% volatile flavor compounds were identified in the essential oil from the L. fischeri. The major compounds were (E)-3-hexenol (30.73%), longiverbenone (13.23%), viridiflorol (12.39%), ${\gamma}$-muurolene (7.32%), limonene (6.12%), and caryophyllene (${\beta}-4.24%$). 99.76% volatile flavor compounds were identified in the essential oil from the L. fischeri var. spiciformis. The major compounds were ledol (42.81%), (E)-15-heptadecenoic acid (33.91%), ${\beta}$-bisabolol (3.23%), viridiflorol (3.08%), and cis-${\alpha}$-farnesene (2.60%). Although the two plants are very similar, the chemical composition of the essential oils was significantly different in quality and quantity. In the case of L. fischeri., it has high contents of monoterpene and sesquiterpene. (E)-3-hexenol, longiverbenone, ${\alpha}$-phellandrene, and ${\alpha}$-myrcene were regarded as the characteristic odorants of L. fischeri, but they were not identified in L. fischeri var. spiciformis. Ledo, (E)-15-heptadecenoic acid, and ${\beta}$-bisabolol were regarded as the characteristic odorants of L. fischeri var. spiciformis, but they were not identified in L. fischeri. The ratio of limonene, ${\gamma}$-muurolene and viridiflorol can be used as an indicator to distinguish between these two plants.

• Journal of Ginseng Research
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• 제21권3호
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• pp.209-213
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• 1997

Sesquiterpenes of Korean ginseng (Panax ginseng C.A. Meyer, KG) and American ginseng (Panax quinquefolium, AG) were Isolated by simultaneous distillation and extraction (SDE) with 30% methanol and n-hexane or adsorption using C18 Sep-Pak . The sesquiterpenes in KG and AG were compared each other by using TLC and GC/MS. Thin layer chromatogram of KG gave 4~5 spots of terpenes colored by vanillin-sulfuric acid, while AG did one major spot. Total ion chromatogram of KG showed about 30 peaks of sesquiterpene having molecular weight 204. Among these, 9 components such as alloaromadendrene, germacrene B, isocaryophyllene, $\alpha$-neoclovene, ${\gamma}$-muurolene and $\beta$-panasinsene together occupied 81.5% of total sesquiterpenes identified. In AG, however, only 3 components, i.e., isocaryophyllene, $\beta$-bisabolene, $\beta$-sesquiphellandrene occupied 79.3% of total sesquiterpenes identified. Especially isocaryophyllene was a dominant component of AG occupying 56.6%. Eight sesquiterpenes, including alloaromadendrene, germacrene B and $\alpha$-humulene, were not detected in AG. These results indicate that sesquiterpenes could be used as indices for the chemical difference between KG and AG.

• 한국식품저장유통학회지
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• 제23권1호
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• pp.63-73
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• 2016

오렌지와 자몽의 휘발성 향기성분을 분석하기 위하여 과육과 과피로 분리하여 각각 SDE 방법으로 휘발성 성분을 추출한 후 GC-MS로 확인하였다. 오렌지의 과육 및 과피의 휘발성 향기성분은 각각 120.55 및 4,510.81 mg/kg이며, 자몽의 과육과 과피는 195.60 및 4,223.68 mg/kg으로 확인되었다. 오렌지와 자몽의 휘발성 향기성분 중 가장 높은 함량으로 확인된 성분은 monoterpene류인 limonene으로 과육은 65.32 및 105.00 mg/kg으로 과피는 3,008.10 및 1,870.24 mg/kg으로 정량되었다. Limonene, sabinene, ${\alpha}$-pinene, ${\beta}$-myrcene, linalool, (Z)-limonene oxide, (E)-limonene oxide 등은 오렌지와 자몽의 공통적인 주요 향기로 확인되었다. 오렌지의 특징적인 향기성분은 valencene이며, 자몽은 (E)-caryophyllene 및 nootkatone으로 확인되었다. $\delta$-3-Carene, ${\alpha}$-terpinolene, borneol, citronellyl acetate, piperitone 및 ${\beta}$-copaene 등은 오렌지에서만 확인된 화합물이며, ${\beta}$-pinene, ${\alpha}$-terpinyl acetate, bicyclogermacrene, nootkatol, ${\beta}$-cubebene 및 sesquisabinene는 자몽에서만 확인되었다. Phenylacetal dehyde, camphor, limona ketone, (Z)-caryophyllene은 과육에서 확인되었으며, ${\alpha}$-thujene, citronellal, citronellol, ${\alpha}$-sinensal, ${\gamma}$-muurolene, germacrene D 등은 과피에서만 확인된 성분이다. 본 연구결과 오렌지 및 자몽의 과육과 과피의 휘발성 향기성분 함량과 조성의 차이를 확인할 수 있었다.

• 한국연초학회지
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• 제20권2호
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• pp.210-217
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• 1998

Volatile flavor components of extracts produced from the domestic angelica root, which are oleoresin and absolutes type, for tobacco flavoring materials were isolated by solvent extraction method and were analyzed by GC and GC/MSD. And then volatile flavor components of oleoresin were compared with volatiles isolated from absolutes. A total of 65 components were identified in the angelica root extracts, from which 41 components were identified in the oleoresin volatiles, contained 15 hydrocarbons, 12 alcohols, 6 acids, 10 esters and 2 miscellaneous components. The major components were hexadecanoic acid (7.79%), methyl palmitate (6.49%), ethyl palmitate (2.02 %) and sesquiterpenes and sesquiterpene alcohols, such as elemol (2.92 %), ${\gamma}$-selinene (2.19%), $\beta$-selinene (2.02%), $\alpha$-eudesmol (3.49%) and $\beta$-eudesmol (6.12%). On the other hand, volatiles of absolutes, from which 60 components were identified, contained 28 hydrocarbons, 14 alcohols, 5 acids, 10 esters and 3 miscellaneous components. The major components were hyrocarbons, such as undecane (5.11 %), dodecane (3.10%) and pentadecane (1.14 %), and $\alpha$-muurolene (1.64 %), ${\gamma}$-selinene (1.49%), $\beta$-selinene (2.12 %), $\alpha$-eudesmol (2.25%), $\beta$-eudesmol (4.87%), hexadecanoic acid (12.67%) and hexanoic acid (1.87 %).

• 생명과학회지
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• 제13권2호
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• pp.206-213
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• 2003

초피의 성숙과정중 향기성분을 조사하고자, 경상남도 밀양시 제약산 일대에서 2001년 6월 2일, 7월 14일 및 9월 11일에 채취한 초피 과피의 향기성분을 CC-MS로 분석한 결과, 6월 2일에는 52종, 7월 14일에는 47종 및 9월 11일에는 44종이 확인되었다. 각각의 채취시기에 대한 구성성분의 종류를 비교하면 terpene류는 6월 2일과 7월 14일에는 myrcene, ${\gamma}$-terpinene, $\alpha$-terpinolene, $\alpha$-phellandrene, $\beta$-caryophyllene 등 8종이 검출되었으나, 9월 11일에는 $\alpha$-phellandrene과 $\beta$-raryophyllene이 검출되지 않았다. Alcohol류는 6월 2일 채취시에는 linalool L, citronellol 등 13종이, 7월 14일과 9월 11일에는 cis-linalool oxide와 piperitol isomer가 추가되어 15종이 검출되었다. Aldyhyde류는 채취시기에 관계없이 citronellal 등 3종이 검출되었으나, 9월 11일에는 citronellal의 함량이 현저히 증가하였으며, ketone류도 cryptone, piperitone 등 5종이 검출되었는데 구성성분의 종류는 채취시기에 관계없이 동일하였으나, 함량의 차이는 있었다. Ester류는 6월 2일에 채취하였을 경우에는 lavandulyl acetate, $\alpha$-terpinenyl acetate 등 6종이 검출되었으나, 7월 14일과 9월 11일에 채취한 과피에서는 [(E)-6,7-ephoxy-3,7-dimethyl-2-octenyl]ester of acetic acid 가 새로이 검출되어 7종이었다. Hyrocarbon류는 $\delta$-cadinene, neopentylideneclohexane 등 7종이었는데, 7월 14일과 9월 11일에는 $\alpha$-muurolene이 추가되어 8종이 검출되었다 초피 과피의 향기성분은 채취시기에 따라서 구성성분의 종류는 물론 농도의 변화가 현저하였다.

• Journal of Ginseng Research
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• 제21권3호
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• pp.214-218
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• 1997

New simple methods for the Isolation of sesquiterpenes from Panax ginseng were developed. First, volatile compounds were isolated by simultaneous distillation and extraction (SDE) with 30% methanol and $\alpha$-hexane instead of water and ethyl ether/pentane (1:1). Secondly, head space volatiles in U-shaped tube at 7$0^{\circ}C$ were passed through C18 Sep-Pak by nitrogen gas streaming and the adsorbed volatiles were fluted by $\alpha$-hexane. TLC analysis showed that the volatile concentrates consisted mainly of terpenes when colored by vanillin-sulfuric and. GC/MS data revealed that approximately 30 sesquiterpenes of molecular weight 204 occupied 81.1% or more of the volatile concentrates isolated by those two newly developed methods. Among these, alloaromadendrene, germacrene B, isocaryophyllene, $\alpha$-neoclovene, ${\gamma}$-muurolene, $\beta$-panaslnsene, and $\alpha$-humulene were identified as being major sesqulterpenes by authentic samples or literatme search Key words : Panax ginseng, volatile compound, sesquiterpene, isolation, new method, GC/MS.

• 한국식품영양과학회지
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• 제41권12호
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• pp.1758-1763
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• 2012

본 연구의 목적은 곰취(Ligularia fischeri)와 한대리곰취(Ligularia fischeri var. spicifoprmis) 정유의 향취 및 화학성분을 비교하는데 있다. 곰취와 한대리곰취의 정유 함량은 각각 0.12%와 0.04%였으며, 역치수준은 각각 0.01%와 0.1%였다. 향수개발전문가에 의해 평가된 곰취 정유의 향취는 citrus, coniferous, green, oily, smoky, wet하였던 반면 한대리곰취 정유의 향취는 balsam, earthy, oily, wet하여 매우 상이하였다. 곰취 정유에는 총 19종의 화학성분이 검출되었는데 탄화수소가 14종(75%), 알코올이 4종(20%), 아세테이트가 1종(5%)이었으며, 주된 화학성분은 L-${\beta}$-pinene(36.02%), D-limonene(25.64%), ${\alpha}$-pinene(24.85%), ${\beta}$-phellandrene(5.39%), 3-carene(3.77%), ${\alpha}$-phellandrene(2.05%)이었다. 한대리곰취 정유에는 총 25종의 화학성분이 검출되었는데 탄화수소 17종(68%), 알코올 4종(16%), 아세테이트 3종(12%), 질소화합물 1종(4%)이었으며, 주된 화학성분은 D-limonene(39.80%), L-${\beta}$-pinene(35.43%) ${\alpha}$-pinene(11.94%), 3-carene(3.70%), ${\beta}$-cubebene(3.51%), ${\beta}$-phellandrene(2.38%)이었다. 한대리곰취 정유에서는 ${\rho}$-cymene, ${\gamma}$-muurolene, ${\gamma}$-cadinene, germacrene D, ingol 12-acetate, butyl 9,12,15-octadecatriene과 nimorazole이 미량 검출되었으나, 곰취 정유에서는 이러한 화학성분들이 검출되지 않았다. 본 연구의 결과 각각 독특한 향취를 갖는 곰취와 한대리곰취 정유는 향장산업제품 개발을 위한 소재로 활용될 수 있을 것이라 판단된다.

• Journal of Ginseng Research
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• 제22권2호
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• pp.73-81
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• 1998

In order to stabilize the price of fresh ginseng by extension of seasonal variation and marketing structure, and to reduce the cost of production by works of intensive and short term, studies were carried out. As fresh ginseng of 4 years old by the MA (modified atmosphere storage) and CA (controlled atmosphere storage) was stored for 12 week at 4$^{\circ}C$, samples were collected after every 1, 2, 3, 4, 6, 8, 12 weeks for processing red ginseng. Chemical characteristics on ginseng steamed red for the quality evaluation are summarized as follows. The composition of free sugar was consisted of fructose, glucose, sucrose, and maltose in fresh ginseng. And small change was revealed in free sugar composition during the storage period. Glucose and sucrose were largely increased in both treatments of MA (modified atmosphere storage) and CA (controlled atmosphere storage) after 4 week, wherein maltose was decreased. Fifteen different amino acids were identified, and total amount of histamine and arginine were over 40%. Phenylalanine was slightly decreased. As the volatile components in control red ginseng, six different ones including triisopropyl benzene were detected. B-1 ($CO_2$ : $O_2$ : N2=6 : 4.90, DF-100) of CA and E-1 (CPP, DF-100) of MA did not shown triisopropyl benzene as the volatile components. And ${\gamma}$-muurolene, guaiaene, and beta-patchoulene were reduced, but the other components showed the trend of increase.

• 한국식품과학회지
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• 제33권2호
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• pp.238-244
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• 2001

본 연구에서는 가열온도에 따른 영귤 과즙의 성분 변화를 조사하여 영귤 가공의 기초 자료로 사용하고자 총산도, $^{\circ}Brix$, pH, 유기산, 유리 아미노산, 비타민 C, 나린진, 헤스페리딘, 네오헤스페리딘 함량, 향기 성분을 분석하였다. 영귤 과즙에는 유기산이 oxalic, citric, malic acid가 존재하였으며, citric acid가 92.8-94.1%로서 대부분을 차지하였고, 그외 malic acid와 oxalic acid 순으로 소량 함유되어 있는 것으로 나타났다. 가열온도가 $40^{\circ}C$에서 $90^{\circ}C$로 증가할수록 총 유기산의 함량은 약간 감소하는 경향을 보여, 가열 전에 비하여 $90^{\circ}C$로 가열 후 약 0.3%가 감소하였다. 영귤 과즙에 존재하는 유리 아미노산은 alanine, threonine, proline, aspargine과 aspartic acid, serine, tyrosine, tryptophane이 주요 유리 아미노산이었다. Arginine, valine, glycine, isoluecine, leucine, histidine등은 소량 존재하였다. 가열함에 따라 유리 아미노산 총량과 개개의 유리 아미노산 함량은 감소하였다. 영귤 과즙에는 비타민 C가 21.3mg% 존재하였으나, 가열함에 따라 점차 감소하여 $90^{\circ}C$에서는 17.3mg%가 존재하였다. 영귤 과즙에 존재하는 나린진, 헤스페리딘, 네오헤스페리딘 함량은 304mg%였으며, 가열함에 따라 297.0mg%로 약간 감소하였다. 영귤 과즙 향기 성분 중 limonene이 가장 많고, ${\gamma}-terpinene,\;{\alpha}-phellandrene$, myrcene, ${\alpha}-pinene$ 등이 주요 향기 구성 성분으로 나타났다. ${\alpha}-Thujene$는 가열하기 전 과즙에는 존재하였으나, $50^{\circ}C$ 이상 가열한 과즙에는 존재하지 않았다. 반면, ${\alpha}-terpinolene$, terpinene-1-ol, ${\beta}-terpineol$, $cis-{\beta}-terpineol$, ${\alpha}-muurolene$, bicyclo(3.2.0)hept-6-ene, mentha-1.4.8-triene 등은 가열하지 않은 원액과 $70^{\circ}C$까지 존재하지 않았으나, $90^{\circ}C$ 가열시에 새로 생성되었다.