• 대한화장품학회지
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• 제28권3호
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• pp.7-39
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• 2002

인체피부의 색소침착에 있어서 다양한 차이는 주로 표피의 멜라닌생성 세포에 의한 멜라닌 합성 비율, 합성된 eumelanin과 pheomelanin의 상대적인 양과 melanocyte에서 keratinocyte로 melanosomes의 이동 속도와 그 방법에서 기인된다. 색소침착은 유전적, 환경적으로 조절되어지는 복합적 특성이다. 많은 관심이 집중되었던 하나의 유전자인 melanocortin 1 receptor 유전자가 있다. 인간집단에서 이 유전자의 다앙한 polymorphism은 색소침착의 다양성에 있어서 중요하다. 자외선(UV)에 대한 노출은 다양한 성장 요인, cytokines과 호르몬의 합성이 증가되고, 표피에서 그들 수용체들의 환경적응등이 나타난다. 색소침착 조절에 관한 정보는 과다색소 침착된 피부손상의 임상치료를 위한 전략들에서 이끌어 냈다. 주된 3개의 전략은 다음과 같다. 1) melanin 합성경로를 방해하는 화합물의 사용 2) eumelanin 합성을 조절하는 호르몬의 구조에서 기인된 peptides 또는 peptide-mimetics개발 3) melanocytes에서 keratinocytes로의 melanosome 이동을 감소시키는 물질의 개발. 이 모든 3가지의 전략은 각각 전체 멜라닌 합성, eumelanin 생성 또는 피부의 멜라닌 단위를 억제시킴으로 미백작용을 유도시킬 것으로 기대되어 진다.

• 대한화장품학회지
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• 제26권2호
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• pp.41-50
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• 2000

- Biochemical studies show that in the process of mixed melanogenesis, cysteinyldopas are produced first which are next oxidized to give pheomelanin. After all of the cysteine is consumed, eumelanin is then deposited on the preformed pheomelanin. - In vitro and in vivo studies show that tyrosinase activity is the most important factor that regulates the switch of melanogenesis, with higher activities increasing melanogenesis, especially eumelanogenesis. - In culturted melanocytes, the tyrosine to cysteine ratio is critical in determining the eumelanin to pheomelanin ratio. - Our HPLC method to analyze eumelanin and pheomelanin has become a useful tool in the study of melanogenesis regulation. There are many problems to be solved before we fully understand the regulation of melanogenesis. Mutations in mouse models are ideal models for studying the genetic and molecular control of melanogenesis. Even in the mouse models, it is not known how cysteine is excluded from being incorporated into melanins in black and other eumelaninc mice, Conversely, it is not known how cysteine is continuously incorporated into pheomelanin in lethal yellow and recessive yellow mice.

• Asian-Australasian Journal of Animal Sciences
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• 제25권7호
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• pp.1029-1037
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• 2012

The present study was designed to investigate the effect of ${\alpha}$-melanocyte-stimulating hormone (${\alpha}$-MSH), nitric oxide (NO) and L-cysteine on melanin production and expression of related genes MC1R, Tyr, Tyrp-1 and Tyrp-2 in muzzle melanocytes of differently colored three native Hanwoo cattle. Muzzle samples were taken from black, brindle and brown Hanwoo and purified melanocytes were cultured with ${\alpha}$-MSH, nitric oxide and L-cysteine at 100 nM, $50{\mu}M$ and 0.07 mg/ml of media respectively. The amounts of total melanin, eumelanin and mRNA expression at Tyr, Tyrp-1, Tyrp-2 and MC1R levels were quantified. ${\alpha}$-MSH and nitric oxide significantly increased (p<0.05) the amount of total melanin in black and brindle whereas eumelanin production in brown Hanwoo muzzle melanocytes. On the contrary, L-cysteine greatly (p<0.05) depressed the eumelanin production in black color but increased in brown. Simultaneously, up regulation of Tyr by nitric oxide and ${\alpha}$-MSH and down regulation of Tyr, Tyrp-2 and MC1R genes by L-cysteine were observed in muzzle melanocytes of all three phenotypes. The results of this study revealed nitric oxide and ${\alpha}$-MSH contribute hyper-pigmentation by enhancing eumelanogenesis whereas L-cysteine contributes to pheomelanin production in different colored Hanwoo muzzle melanocytes.

• Mass Spectrometry Letters
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• 제9권3호
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• pp.81-85
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• 2018

In this study, the chemical composition of bacterial melanin isolated from the Streptomyces glaucescens strain was elucidated by ultra-high-resolution Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry. Ultra-high-resolution mass profiles of the microbial melanin product were acquired using a 15 Tesla FT-ICR mass spectrometer in positive and negative ion modes via electrospray ionization to obtain more complete descriptions of the molecular compositions of melanin-derived organic constituents. A mass resolving power of 500,000 (at m/z 400) was achieved for all spectra while collecting 400 scans per sample with a 4 M transient. The results of this analysis revealed that the melanin pigment isolated from S. glaucescens predominantly exhibits CHON and CHO species, which belong to the proteins class of compounds, with the mean C/O and C/N ratios of 4.3 and 13.1, thus suggesting that the melanin could be eumelanin. This analytical approach could be utilized to investigate the molecular compositions of a variety of natural or synthetic melanins. The compositional features of melanins are important for understanding their formation mechanisms and physico-chemical properties.

• 대한화장품학회지
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• 제28권3호
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• pp.91-108
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• 2002

미백제는 기미와 태양광선노출에 의한 색소침착반과 같은 색소불균형이 주로 나타나는 동양 여성들에 특히 관심이 많다. 이러한 색소침착의 불균형은 UV에 의해 더 심해지기 때문에 미백제는 멜라닌합성을 억제시키거나 UV에 의해 활성화된 signal을 억제함으로써 효과가 나타난다. Eumelanin은 UV에 의해 유도된 DNA 손상을 보호하므로 UV에 의해 유도된 DNA손상을 감소시키는 물질이 이상적인 미백제가 된다. 새롭게 합성된 항산화제인 $\alpha$-tocophenyl ferulate의 효과는 UV에 의해 손상된 DNA damage에 의한 보호 효과와 멜라닌 합성을 억제시킴으로서 나타난다. Chemical peeling과 복합적으로 색소 반점을 치료하는 lightning agent의 효과에 대한 결과를 보고하였으며 색소 반점의 개선을 정량적으로 평가하는 새롭게 개발된 facial image analyzer를 소개할 것이다.

• 패션비즈니스
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• 제12권6호
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• pp.23-33
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• 2008

The physico-chemical characteristics by bleaching treatments were assessed by several instrumental analyses such as surface morphology, chemical structural change, color change as well as tensile strength. The change of morphological characteristic was observed through scanning electron microscope(SEM). The observation of the fine structure on hair surface by SEM showed the bleached hair had much damaged to hair cuticle, and some of cuticle surface were worn away. To investigate the chemical structural changes in hair keratin, the cross-sections of hair samples were directly analysed using Fourier transform infrared microspectroscopy(FT-IRM). The results showed the cysteic acid S=O band intensity was distinctively increased by performing the bleaching treatment. The cleavage of cystine was appeared to proceed primarily through the sulfur-sulfur (-S-S-) fission whereby cysteic acid was formed as a principal oxidation products. The distribution of amide I band in hair keratin was determined by attenuated total reflectance(ATR) FT-IR mapping image. The results showed that the outer side of hair cortex was more damaged than the inner side of the hair cortex. Also, during chemical bleaching of the hair with alkaline peroxide, the hair was turned to reddish yellow due to the oxidative degradation of eumelanin. This means the eumelanin is more unstable than pheomelanin in chemical oxidation. With bleaching, the tensile strength was also reduced as a results of the chemical oxidation.

• Journal of Animal Science and Technology
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• 제49권1호
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• pp.147-154
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• 2007

한우와 제주흑우의 모색 특성과 양적 수치화를 위하여 분광광도법적 분석을 수행하였다. 분석 결과 제주흑우의 총 melanin 함량은 같은 흑색 품종인 Holstein과 Angus에 비해 유의적으로 낮았고 한우나 적색 품종 보다는 높은 수준을 보였다(P<0.001). 한우의 총 melanin 함량은 적색 품종에 비해 유의적으로 낮았고 한우×Charolais 교잡종에 비해 높았다(P<0.001). 전체 melanin 중 eumelanin, pheomelanin의 상대적 수준을 분석한 결과 Angus, 제주흑우, Red Holstein과 한우 각각 0.382, 0.359, 0.112와 0.124 이었다. 품종별 모발 melanin 색소 함량 분석결과는 분광광도법적 분석이 소 품종별 모색의 양적 수치화 및 특성 비교에 이용 가능하고 한우와 제주흑우의 주요 모색 관련 유전자 연구의 기초 자료로 유용함을 보여주고 있다.

• Asian-Australasian Journal of Animal Sciences
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• 제23권4호
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• pp.444-449
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• 2010

The aim of this study was to measure the hair melanins of various colors and to find the relationship between the quantity of melanins and hair color phenotypes in alpacas. According to the Munsell color system, 3 healthy alpacas were selected for each of the 22 different hair color phenotypes (66 alpacas altogether). Alpaca hair was taken from the lateral thoracic region and then dissolved with different solutions to obtain melanins. The values of alkali-soluble melanins (ASM), eumelanin (EM) and pheomelanin (PM) were measured by spectrophotometric assay, and labeled as Sp.ASM, Sp.EM and Sp.PM, respectively. Data were analyzed using SPSS11.5 software. Results showed that average Sp.ASM and Sp.PM were increased as the color deepened from white to black, ranging from 0.500 to 4.543 for Sp.ASM and from 0.268 to 1.457 for Sp.EM. However, average Sp.PM had no such apparent relationship with color. Based on the value of Sp.ASM and EM, 7 hues were produced and gray was a single hue. Most of the data were in a normal distribution (p>0.10). ANOVA analysis showed that mean values of Sp.ASM, Sp.EM and Sp.PM were significantly different (p<0.05). The results also showed that Sp.ASM was positively correlated with Sp.EM but the correlation between Sp.ASM and Sp.PM was not significantly different from 0. It is concluded that EM is the major constituent of alpaca hair melanin; there is a significant correlation among ASM, EM and alpaca hair colors, and EM is the most reliable parameter for distinguishing these groups.

• Asian-Australasian Journal of Animal Sciences
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• 제26권5호
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• pp.625-629
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• 2013

The melanocortin 1 receptor (MC1R) gene is related to the plumage color variations in chicken. Initially, the MC1R gene from 30 individuals was sequenced and nine polymorphisms were obtained. Of these, three and six single nucleotide polymorphisms (SNPs) were confirmed as synonymous and nonsynonymous mutations, respectively. Among these, three selected SNPs were genotyped using the restriction fragment length polymorphism (RFLP) method in 150 individuals from five chicken breeds, which identified the plumage color responding alleles. The neighbor-joining phylogenetic tree using MC1R gene sequences indicated three well-differentiated different plumage pigmentations (eumelanin, pheomelanin and albino). Also, the genotype analyses indicated that the TT, AA and GG genotypes corresponded to the eumelanin, pheomelanin and albino plumage pigmentations at nucleotide positions 69, 376 and 427, respectively. In contrast, high allele frequencies with T, A and G alleles corresponded to black, red/yellow and white plumage color in 69, 376 and 427 nucleotide positions, respectively. Also, amino acids changes at position Asn23Asn, Val126Ile and Thr143Ala were observed in melanin synthesis with identified possible alleles, respectively. In addition, high haplotype frequencies in TGA, CGG and CAA haplotypes were well discriminated based on the plumage pigmentation in chicken breeds. The results obtained in this study can be used for designing proper breeding and conservation strategies for the Korean native chicken breeds, as well as for the developing breed identification markers in chicken.

• Journal of Microbiology and Biotechnology
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• 제27권9호
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• pp.1692-1700
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• 2017

Ralstonia solanacearum causes bacterial wilt in a wide variety of host plant species and produces a melanin-like blackish-brown pigment in stationary phase when grown in minimal medium supplemented with tyrosine. To study melanin production regulation in R. solanacearum, five mutants exhibiting overproduction of melanin-like pigments were selected from a transposon (Tn) insertion mutant library of R. solanacearum SL341. Most of the mutants, except one (SL341T), were not complemented by the original gene or overproduced melanins. SL341T showed Tn insertion in a gene containing a conserved domain of eukaryotic transcription factor. The gene was annotated as a hypothetical protein, given its weak similarity to any known proteins. Upon complementation with its original gene, the mutant strains reverted to their wild-type phenotype. SL341T produced 3-folds more melanin at 72 h post-incubation compared with wild-type SL341 when grown in minimal medium supplemented with tyrosine. The chemical analysis of SL341T cultural filtrate revealed the accumulation of a higher amount of homogentisate, a major precursor of pyomelanin, and a lower amount of dihydroxyphenylalanine, an intermediate of eumelanin, compared with SL341. The expression study showed a relatively higher expression of hppD (encoding hydroxyphenylpyruvate dioxygenase) and lower expression of hmgA (encoding homogentisate dioxygenase) and nagL (encoding maleylacetoacetate isomerase) in SL341T than in SL341. SL341 showed a significantly higher expression of tyrosinase gene compared with SL341T at 48 h post-incubation. These results indicated that R. solanacearum produced both pyomelanin and eumelanin, and the novel hypothetical protein is involved in the negative regulation of melanin production.