• 한국식품영양학회지
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• 제11권5호
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• pp.506-512
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• 1998

In order to replance systhetic colors by natural colors as food additive, properties of Gardenia yellow color and Gardenia blue color were compared with Food yellow No. 4 and Food blue No. 1. Color differeance between Food yellow No. 4 and Gardenia yellow color was 7.55. Thermal stability of Food yellow No. 4 was above 99%. On the other hand, in case of Gardenia yellow color, showed adove 90% of residual color units in 8$0^{\circ}C$$\times$30min and 10$0^{\circ}C$$\times$30min at pH 7.0 but 75% in 121$^{\circ}C$$\times$15min. Difference of light stability between Food yellow No. 4 and gardenia yellow color was about 18%. Addition of ascorbic acid was increased about 6% in light stability. Color difference between Food blue No. 2 and Gardenia blue color was 107. Thermal stability of Food blue No. 2 was above 99%. But Gardenia blue color showed 92% of residual color units in 8$0^{\circ}C$$\times$30min and 10$0^{\circ}C$$\times$30min at pH 7.0 but 90% in 121$^{\circ}C$$\times$15min. Difference of light stability between Food blue No. 4 and Gardenia blue color was about 8%. Addition of -tocopherol was increased about 4% in light stability of Gardenia blue color.

• Molecular & Cellular Toxicology
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• 제5권3호
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• pp.257-264
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• 2009

Gardenia yellow, extracted from gardenia fruit, has been widely used as a coloring agent for foods, and thus, safety of its usage is of prime importance. In the current study, short-term genotoxicity assays were conducted to evaluate the potential genotoxic effects of gardenia yellow. The gardenia yellow used was found to contain 0.057 mg/g of genipin, a known biologically active compound of the gardenia fruit extract. Ames test did not reveal any positive results. No clastogenicity was detected by a chromosomal aberration test, even on evaluation at the highest feasible concentration of gardenia yellow. Gardenia yellow was also shown to be non-genotoxic using an in vitro comet assay and a micronucleus test with L5178Y cells, although a marginal increase in DNA damage and micronuclei frequency was reported in the respective assays. Additionally, in vivo micronucleus test results clearly demonstrated that oral administration of gardenia yellow did not induce micronuclei formation in the bone marrow cells of male ICR mice. Taken together, our results indicate that gardenia yellow is not mutagenic to bacterial cells, and that it does not cause chromosomal damage in mammalian cells, either in vitro or in vivo.

• 한국의상디자인학회지
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• 제19권1호
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• pp.135-145
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• 2017

In order to analysis on color difference of yellow natural dyes, I have dyed cellulose and protein fabrics. The results of experiment have been analysed by wavelength of maximum absorption, amounts of dye uptake, color difference, Hunter's value and Munsell's value. The results from these analyses are as follows : Bud of pagoda tree, Amur cork, and Curcuma showed greenish yellow color, Gardenia Jasminoides showed reddish yellow color. Barberry root showed reddish yellow color with post-mordanting method on cellulose fabric. Moreover, Dupioni silk was dyed in reddish yellow color by Barberry root and Rhubarb. In addition to Chroma index, Gardenia Jasminoides and Curcuma showed clear color overall. However, dyeing rayon and silk by Barberry root, and dyeing silk by Rhubarb showed clear color. Comparing all the results to actual dyed materials, Bud of pagoda tree had small dye uptake, and both ${\Delta}a$ and ${\Delta}b$ value were short which can't recognized the yellow color easily. Dye uptake of Amur cork and Gardenia Jasminoides was small just like Bud of pagoda tree. However, ${\Delta}b$ value order was Gardenia Jasminoides>Amur cork>Bud of pagoda tree. Therefore, Gardenia Jasminoides recognized reddish yellow because of big value of red color and yellow color. In case of Barberry root and Rhubarb which have larger dye uptake, Baberry root recognized yellow color on rayon only, and couldn't recognized yellow color on bleached cotton fabric, ramie, silk, and dupioni silk. Rhubarb recognized yellow color on rayon with pre-mordanting method only, but recognized silk and dupioni silk as brown like color. Moreover, we could not analyze color by dye uptake, Lab, and H(v/c) for Barberry root and Rhubarb. As a result, I think we need to attach color table for the research paper which handled the color of dyeing materials.

• Journal of the Korean Wood Science and Technology
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• 제48권2호
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• pp.154-165
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• 2020

To assign the functionality of the regenerated fiber from waste MDF(wMDF) made of pitch pine, we examined the dyeing characteristics of natural dyes, sappan wood as a polychromatic natural red series, monochromatic gardenia as a yellow series, and indigo blue series. For nonemordanting dye, the colors of regenerated fiber dyed by sappan wood and gardenia were reddish yellow (YR) and yellow (Y) series, respectively, and dyeing conditions were appropriate a 30 ~ 50 g/L of dyeing materials at 60 ℃ for 60minutes of dyeing time. We obtained regenerated woody dyed fibers (Re-WDF), YR to the red (R) series by premordanting with Al and Cu mordant for sappan wood and the purplish red (RP) series by Fe premordanting. In the case of gardenia, only Y series colors were developed in nonemordanting dye or all three mordants. Indigo dye produced Re-WDF with greenish yellow (GY) tone at 1%, green (G) tone at 3%, and blue (B) tone at 5% concentration or more. Re-WDF with indigo showed the best light fastness followed by sappan wood and gardenia. In particular, the light fastness of Re-WDF with gardenia was very poor. The light fastness was somewhat improved by premordanting(Fe>Cu>Al) both sappan wood and gardenia dyes.

• 한국식품과학회지
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• 제30권2호
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• pp.319-323
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• 1998

치자의 황색소를 L. plantalium, V. vulinficus, P. aeruginosa, S. mutans, B. subtilis, S. epidermidis, S. typhimurium, S. aureus 등 8종의 균주의 배지에 첨가하고 배양하면 청녹색계 색소로 변환된다. 미생물에 의해 변환된 색소의 분광학적 성질을 경시적으로 추적하면 색소의 변환형태는 3군으로 나뉘어지며, 색차계로 측정된 ${\Delta}E$ 값의 변환형태도 그러하였다. 청녹색계색소로의 변환속도는 균주에 따라 차이를 보였는데 8종의 미생물중 S. epidermidis는 가장 빨라 배양 16시간에 색소변환이 완성되었다. 치자황색소와 변환된색소는 $H_2O-MeOH$ 용매계에 의한 Amberlite XAD-4 column chromatography에 의해 완전히 분리되었으며, 광과 열에 대한 저장안정성은 치자황색소보다 변환된 색소가 보다 안정함을 나타냈다.

• 한국식품과학회지
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• 제31권1호
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• pp.106-109
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• 1999

S. epidermidis에 의해 치자황색소에서 변환된 청녹계색소와 치자황색소의 저장안정성에 미치는 광, 온도, pH, 무기이온에 의한 영향을 조사하였다. 두 색소는 광과 $40^{\circ}C$ 이상의 온도조건에서 변색에 영향을 받았으나, 변환된 색소가 보다 안정성이 있으며, 광에 의한 영향은 green filter에 의해 감소시킬 수 있었다. pH와 무기이온에 의한 영향은 두 색소 모두 작았다.

• 한국식품영양학회지
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• 제11권1호
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• pp.72-76
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• 1998

세균을 이용한 복귀돌연변이 시험계는 Salmonella typhimurium 히스티딘 요구성 변이주를 이용하여 염기대치환(base change)의 돌연변이를 검출하는 S. typhimurium TA100, TA1535와 frameshift형의 돌연변이를 검출하는 S. Tphimurium TA98, TA1537로 구성되어 있으며, 화학물질의 변이원성에 의하여 히스티딘 비요구성으로 복귀하는 돌연변이를 검토하는 시험계로 널리 이용되고 있다. 시험결과, Yellow pigment는 S. typhimurium에 대한 독성도 나타나지 않았으며, 배지 1$m\ell$당 200$\mu\textrm{g}$ 이하의 모든 농도에서 S-9 Mix(대사활성계)의 유무에 관계없이 S. typhimurium 모든 변이주에서 히스티딘 요구성에 대한 복귀돌연변이를 유발하지 않는 물질로 판단되었다. 이상의 결과로부터 치자황색색소는 S. typhimurium을 이용한 복귀돌연변이 시험에서 유전독성이 없는 물질로 사료되었다.

• 한국식품영양학회지
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• 제11권1호
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• pp.68-71
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• 1998

현재 사용중인 합성색소 중에서 사용빈도가 가장 높은 합성색소 중의 하나인 황색 4호의 대체용 천연색소를 치자에서 추출하였으며 추출조건은 추출온도 7$0^{\circ}C$, 추출시간 48시간, 추출 pH 7.0 및 기질농도는 10%였으며 이때의 추출수율은 61%였다. 추출한 조색소를 정제하기 위하여 활성백토를 사용하여 정제를 실시하였으며, 조색소액에서 배당체 성분과 색소성분을 각각 단일 peak로 분리하였다. 조색소액을 정제한 후 정제도는 약 27배 증가하였고, 수율은 96%로 높게 나타났다.

• 한국식품영양학회지
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• 제10권2호
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• pp.241-245
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• 1997

천연식용색소를 제조하기 위하여 치자를 이용하여 색소추출의 최적조건과 황색 4호와의 내열성 및 내광성을 조사하였다. 에탄올을 추출용매로 사용한 경우 색소추출 최적조건은 추출온도 4$0^{\circ}C$, 추출시간 42시간, 추출 pH 7.0 및 기질농도 10%였다. 물추출의 경우 추출온도는 7$0^{\circ}C$, 추출시간 48시간, 추출 pH 7.0 및 기질농도 10%였다. 최적조건에서의 추출수율은 에탄올의 경우 75%였고, 물추출의 경우는 63%로 나타났다. 황색 4호와 치자 황색소의 내열성 및 내광성을 비교 검토한 결과, 황색 4호는 내열성과 내광성이 모두 98% 이상으로 나타났으나, 치자 황색소의 경우는 내열성은 62%, 내광성은 90%로 나타났다.

• Journal of Microbiology and Biotechnology
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• 제1권2호
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• pp.142-149
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• 1991

Gardenia callus was induced in MS medium containing $10{\;}{\mu}M$ of 2,4 diphenoxy acetic acid (2,4-D), $1{\;}{\mu}M$ kinetin, and 3% sucrose in the dark. $B_5$ medium was identified to be the most adequate medium for cell growth. Indole-3-acetic acid (IAA) was better growth regulator than 2,4-D not only for cell growth but slso for carotenoid production. Ligt also played a critical role on synthesis of carotenoid. Gardenia cells grown in $B_5$ medium could utilize a polysaccharide, soluble starch, as a carbon source. The cell growth was stimulated in $B_5$ medium fortified with 0.2% yeast extract. The optimum pH for cell growth was 5.7. High density cultures can be maintained by increasing inoculum size and medium concentration accordingly. Specific growth rate and mass doubling time were 0.095 $day^{-1}$ and 7.3 days, respectively. The cell immobilized in alginate tends to formulate more enlarged vacuoles containing yellow pigment compared with those of suspended cell. Carotenoid content of immobilized cell was about $264.4{\;}{\mu}g/g$ fresh weight (F.W.) corresponding twice of the content of suspended cell ($112.08{\;}{\mu}g/g$ F.W.). The color of gardenia cell was shifted from yellow to red when carbohydrase-secreting fungus, Trichoderma reesei, was co-cultivated with gardenia cells.