• Journal of Sericultural and Entomological Science
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• v.52 no.1
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• pp.25-32
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• 2014

We produced the transgenic silkworm that expressed the enhanced blue fluorescent protein (EBFP) in the cocoon of silkworms. The EBFP fusion protein, each with N- and C-terminal sequences of the fibroin H-chain, was designed to be secreted into the lumen of the posterior silk glands. The expression of the EBFP/H-chain fusion gene was regulated by the fibroin H-chain promoter. The use of the $3{\times}P3$-driven DsRed2 cDNA as a marker allowed us to rapidly distinguish transgenic silkworm. A mixture of the donor and helper vector was micro-injected into 300 eggs of silkworms, Baegokjam. We obtained 5 broods. The cocoon displayed blue fluorescence, proving that the fusion protein was present in the cocoon. Also, the presence of fusion proteins in cocoons was demonstrated by SDS-PAGE and western blot analysis. Accordingly, we suggest that the EBFP fluorescence silk will enable the production of the silk-based biomaterials.

• Journal of Sericultural and Entomological Science
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• v.52 no.2
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• pp.102-109
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• 2014

We constructed the fibroin H-chain expression system to produce enhanced yellow fluorescent proteins (EYFP) in the silk of transgenic silkworm. Fluorescent silk could be made by fusing EYFP cDNA to the heavy chain gene and injecting it into a silkworm. The EYFP fusion protein, each with N- and C-terminal sequences of the fibroin H-chain, was designed to be secreted into the lumen of the posterior silk glands. The expression of the EYFP/H-chain fusion gene was regulated by the fibroin H-chain promoter. The yellow fluorescence proving that the fusion protein was present in the silk. Accordingly, we suggest that the EYFP fluorescence silk will enable the production of novel biomaterial based on the transgenic silk.

• Journal of Sericultural and Entomological Science
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• v.49 no.2
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• pp.77-80
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• 2007

Silk fibroin/poly (vinyl pyrrolidone) conjugates were prepared and characterized through differential thermal calorimeter and thermogravimetry. The glass transition temperature (Tg) of poly (vinyl pyrrolidone) was not changed by reaction with silk fibroin. However, abnormal exothermic peak was observed at the silk fibroin/poly (vinyl pyrrolidone) conjugates. Thermogravimetric analysis showed that thermal stability of silk fibroin was relatively increased by reaction with PVP.

• Proceedings of the Culinary Society of Korean Academy Conference
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• 2004.04a
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• pp.51-65
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• 2004

1. 일반 성분에서 실크 프로테인은 쌀가루에 비해 단백질은 91.22%로 매우 높은 함량을 보였다. 2. pH는 쌀가루와 실크 프로테인이 비슷한 약산성을 나타냈다. 3. 총 유리당 함량을 보면 쌀가루에 비해 실크 프로테인이 매우 낮음을 알 수 있었다. 4. 총 아미노산 함량에서는 실크 프로테인이 쌀가루보다 13배나 높은 함량을 나타내었다. 5. 쌀가루의 아미노산 조성은 glutamic acid 함량이 가장 높았으며, 실크 프로테인은 glycine이 가장 높았다. 6. 특히 실크프로테인은 곡류의 제한 아미노산인 lysine이 높게 함유되어 있어 곡류 가공 조리제품에 이의 첨가는 부족된 lysine 함량의 보풍에도 큰 효과가 있을 것으로 사료된다. 7. 실크 프로테인 첨가수준에 따른 절편의 관능적 품질변화에서 색택(color)은 무첨가군 및 1% 첨가군를 가장 선호하는 것으로 나타났으며, 종합적 기호도(overall acceptance)는 무첨가구 및 1~3% 첨가구를 선호하는 것으로 나타났다.

• Proceedings of the Korean Fiber Society Conference
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• 2003.04a
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• pp.275-278
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• 2003

실크 세리신은 누에(Bombyx mori)로부터 얻어지는 천연 거대분자 단백질로서, 누에고치실의 20~30%를 차지하고 있다. 세리신은 외부로의 자극으로부터 피브로인을 보호하는 역할을 하지만, 견사나 견직물을 얻기 위해서는 정련 공정에서 반드시 제거하게 된다. 현재 생산 현장에서는 비누/알칼리 정련법으로 세리신을 제거하고 있는데, 정련 폐액중에 포함되어 있는 세리신 단백질에서 분해된 각종 아미노산과 비누 및 강알칼리 약제로 인해 환경오염의 주된 원인이 되고 있다. (중략)

• Journal of Sericultural and Entomological Science
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• v.51 no.2
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• pp.197-200
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• 2013

Silk fibroin is a natural biomaterial that has the biocompatibility and other many advantages. But as a silk fibroin membrane thickness increases, the transparency becomes more opaque. Because the transparency of membranes tissue such as the cornea and dura mater are necessary, transparent membrane is required to replace these transparent membranes. In this study, we fabricated blending silk fibroin membranes that made by mixing the various inorganic salts or polymer in an aqueous solution of silk fibroin. The transparency of the membranes were analyzed. the transparency of these membranes is very different, depending on the mixed materials. Inorganic salts mixed silk membrane was more transparent than the polymer mixed one. Especially, the silk fibroin membrane with calcium chloride was very transparent. We showed the possibility of blending silk fibroin membrane, which can be used in perfect transparent membrane such as the cornea. In the future, we expect that the transparent blending silk fibroin membrane can be used in various medical applications.

• Proceedings of the Korean Society of Sericultural Science Conference
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• 2003.04a
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• pp.57-57
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• 2003

세리신은 실크의 25%를 차지하는 단백질이다. 대부분 정련과정을 통하여 제거되지만 이를 재활용하려는 시도는 꾸준히 진행되고 있다. 특히 천연보습인자 (NMF)인 세린을 많이 함유하고 있어 화장품 분야로의 응용이 기대되며, 최근에는 세리신을 합성섬유에 코팅하는 skin care 가공도 개발되었다. 그러나 세리신은 젤화가 일어나고 동결건조 후에는 용해도가 감소하는 경향이 있다. (중략)

• Journal of the Korean Society of Food Science and Nutrition
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• v.36 no.5
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• pp.554-562
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• 2007

Ceramide rich intercellular lipid lamellae are thought to be particularly important in maintaining the structural integrity of epidermal barrier. Ceramide is synthesized de novo by serine palmitoyltransferase (SPT) phospholipid intermediates, serine and palmitic acid persist within the stratum corneum. The ceramide which is synthesized is degraded with fatty acid and sphingosine by degradative enzyme ceramidase. The depletion of ceramide in stratum corneum was reported in the atopic dermatitis. As an effort to search for the dietary source for improving the level of ceramide in epidermis, the dietary effects of various-typed silk protein were compared. Seventy male NC/Nga mice, an animal model of atopic dermatitis, were divided into seven groups: group CA as an atopic control with control diet, group S: 1% crude sericin diet, group F: 1% crude fibroin diet, group PS : peptide pattern of sericin(Mw 5000), group PF: peptide pattern of fibroin (Mw 1500), group AS: manufactured the same as amino acid profile of sericin and group AF: manufactured the same as amino acid profile of fibroin. Ten male BALB/c mice were served as group C (control group) control diet. All mice were fed on diet and water ad libitum for 10 weeks. Dry skin condition was established in group CA as ceramide content was decreased. Despite a marked decrease of mRNA and prorein expression of SPT, enzyme do novo synthesis, ceramide content of group S was dramatically increased by inhibiting the mRNA and protein expression of degradative enzyme ceramidase. However, dietary supplementation of crude silk fibroin protein (group F) and in other groups that were supplemented with either amino acid or peptide type of sericin or fibroin did not increase the level of ceramide. Together, our data demonstrate that dietary supplementation of crude sericin is more effective at improving ceramide level in epidemis of NC/Nga mice.

• Journal of Sericultural and Entomological Science
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• v.48 no.1
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• pp.6-10
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• 2006

Recently, B. mori proteins such as silk fibroin and silk sericin have been found to have a water-holding capacity, anti hydrogen peroxide toxicity, antioxidant activity and tyrosinase-inhibitory activity (Yeo 2006, Kurioka 1999 & 2004), implying its potential usefulness of the application for cosmetic and functional food(Yamazaki 1999 & Une 2000). We are tried to application for dietary resources of B. mori silk fibroin and sericin that were prepared to some of different molecular cutting these resources by preparative recycling HPLC system. In our studies with rats have demonstrated that consumption of these silk proteins are being prevents constipation effect and it is maybe enhances intestinal absorption of water and dietary effects. These some of useful results further suggest a usefulness of sericin as dietary resources for health.

• Journal of Sericultural and Entomological Science
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• v.50 no.2
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• pp.87-92
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• 2012

We constructed the fibroin H-chain expression system to produce Discosoma sp. red fluorescent protein variant2 (DsRed2) in transgenic silkworm cocoon. Fluorescent cocoon could be made by fusing DsRed2 cDNA to the heavy chain gene and injecting it into a silkworm. The DsRed2 fusion protein, each with N- and C-terminal sequences of the fibroin H-chain, was designed to be secreted into the lumen of the posterior silk glands. The expression of the DsRed2/H-chain fusion gene was regulated by the fibroin H-chain promoter. The use of the 3xP3-driven EGFP cDNA as a marker allowed us to rapidly distinguish transgenic silkworms. The EGFP fluorescence became visible in the ocelli and in the central and peripheral nervous system on the seventh day of embryonic development. A mixture of the donor and helper vector was micro-injected into 1,020 Kumokjam, bivoltin silkworm eggs. We obtained 6 broods. The cocoon was displayed strong red fluorescence, proving that the fusion protein was present in the cocoon. Accordingly, we suggest that the DsRed2 fluorescence silk will enable the production of novel biomaterial based on the transgenic silk.