KR810001586B1 - Degumming method of silk by fermentation - Google Patents
Degumming method of silk by fermentation Download PDFInfo
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- KR810001586B1 KR810001586B1 KR1019800003670A KR800003670A KR810001586B1 KR 810001586 B1 KR810001586 B1 KR 810001586B1 KR 1019800003670 A KR1019800003670 A KR 1019800003670A KR 800003670 A KR800003670 A KR 800003670A KR 810001586 B1 KR810001586 B1 KR 810001586B1
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- South Korea
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- silk
- fermentation
- degumming
- refining
- bacillus megaterium
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01C—CHEMICAL OR BIOLOGICAL TREATMENT OF NATURAL FILAMENTARY OR FIBROUS MATERIAL TO OBTAIN FILAMENTS OR FIBRES FOR SPINNING; CARBONISING RAGS TO RECOVER ANIMAL FIBRES
- D01C3/00—Treatment of animal material, e.g. chemical scouring of wool
- D01C3/02—De-gumming silk
Abstract
Description
본 발명은 견사방적의 원료가 되는 부잠사(副蠶사)를 정련함에 있어서 배시러스ㆍ메거테리움 SY-7(Bacillus megaterium SY-7) 세균을 이용하여 종래의 부잠사 정련방법보다 정련시간이 단축되고 정련도가 균제하며 잔지량(殘脂量)이 적고, 견층(繭層) 또는 생피저(生皮苧)의 베이브(Bave)는 상호간의 섬조유리(纖條遊離)가 거의 완전하며, 인장강도와 섬유의 백색도가 양호한 견섬유를 얻을 수 있으며, 또한 화학처리에 의한 후처리공정도 생략할 수 있어 경비절감과 황변화를 방지할 수 있는 등의 이점이 있는 견사 방적원료의 정련방법에 관한 것이다.The present invention uses Bacillus megaterium SY-7 (Bacillus megaterium SY-7) bacteria in refining silkworms as raw materials of silk-spun yarns. It is shortened, uniformly refined and has a small amount of residue. The silk or silk-shaped babe has almost complete thread glass, and the tensile The present invention relates to a method for refining silk spinning raw materials, which has advantages of being able to obtain a silk fiber having good strength and whiteness, and also after-treatment by chemical treatment, which can reduce cost and prevent sulfur change. .
종래 부잠사의 정련방법에서는 중성비누, 탄산소다, 계면활성제등에 의한 화학적처리방법과 발효에 의한 정련 방법등이 있었으나, 전자는 섬유에 손상을 주게 되므로 인장강도가 현저하게 저하되며 황갈색으로 변화되기 쉬우므로 채용되고 있지 않으며, 후자는 자연발효에 의하여 일반적으로 행하여지고 있으나 소요 정련시간이 길고 견층 또는 생피저의 베이브는 상호간의 유리가 불량하고 잔지율이 높이며 착색 오염되기 쉬우므로 후처리(정련)공정을 거쳐야 하는 여러 가지 단점을 가지고 있었다.Conventional refining methods of Bujasa include chemical treatment methods such as neutral soap, sodium carbonate, and surfactants, and refining methods by fermentation. However, since the former damages the fiber, the tensile strength is significantly lowered and it is easy to change to yellowish brown. Since the latter is generally performed by natural fermentation, the required refining time is long, and the skin of silk layer or raw skin is poor in glass, high residue rate and easy to be stained. There were a number of disadvantages to go through.
본 발명은 상기와 같은 결점을 해결하기 위한 것으로 보다 상세히 설명하면 다음과 같다.The present invention is to solve the above-mentioned drawbacks described in more detail as follows.
본 발명에서 이용한 배시러스ㆍ메거테리움 SY-7 세균은 생피저(부잠사) 50g에 증류수 5ℓ를 넣고 1.2㎏/㎠ 압력하에서 120분동안 끓여 세리신 추출액하고, 이 액을 여과한 후, 전액량(全液量)을 5ℓ가 되도록 증류수로 보충하여 약 0.2%의 세리신 추출액을 만들었다. 그 여액(濾液) 1ℓ당 비프ㆍ익스트랜트(Beef extract) 3g, 펩톤 (Pepton) 10g, 소금 3g을 넣고, pH 6.8-7.4로 조제한 배지(培地, 고체 배지의 경우는 아가(Agar) 1.5%를 첨가)를 300ml 삼각플라스크에 30ml씩 놓고 각종의 분리원(分離源, 발효조(槽) 폐액, 각종 부잠사 부스러기, 페니이 부스러기, 흙, 시궁창물등)을 1g씩 넣고 34℃에서 112시간 배양후 평판(平板) 분리법에 의하여 순수분리한 후, 이들 가운데서 퍼브로인에 대하여 손상이 거의 없고, 푸로티아제(Protease)의 역가가 가장 높은 것을 선정한 것으로, 이 균은 단간균(短桿菌)으로서 0.6-0.8×3.0-3.8μ 정도의 크기이며, 활동성 그램 양성균으로 생육 최적온도는 31-36℃, pH는 6.8-7.7이다.Bacillus megaterium SY-7 bacteria used in the present invention, 5 g of distilled water was added to 50 g of fresh skin (Buxamsa), boiled under 1.2 kg / cm 2 pressure for 120 minutes, and the sericin extract was filtered. Distilled water was replenished so that 5 liters of it was made into about 0.2% of sericin extract. 1 g of Beef extract, 10 g of Pepton, and 3 g of salt were added per 1 liter of the filtrate, and 1.5% of Agar in the case of a solid medium prepared at pH 6.8-7.4 was used. 30 ml each of 300 ml Erlenmeyer flasks, and put 1 g of various separation sources (fermentation tank waste liquor, various sub-silsa wastes, penny scraps, soil, gutter, etc.) and incubate at 34 ° C for 112 hours. After separation by pure water separation method, there was little damage to perbroin among them, and the highest titer of protease was selected. This bacterium was 0.6-0.8 It is about 3.0-3.8μ in size. It is active gram-positive bacteria, and the optimum growth temperature is 31-36 ℃ and pH is 6.8-7.7.
부잠사를 정련할 때는 배시러스ㆍ메거테리움 SY-7 균주(菌株)를 이용하여 온도 31-35℃, pH 6.5-7.5로 조절하면서 실시하였는데 그 실시예는 다음과 같다.When refining Bujasa was carried out by controlling the temperature to 31-35 ℃, pH 6.5-7.5 using the Bacillus megaterium SY-7 strain (Example) is as follows.
[실시예]EXAMPLE
부잠사 1㎏에 수돗물 5ℓ를 넣고, 85-95℃에서 3-4시간 처리하여 세리신을 추출한 액 1ℓ당, 비프ㆍ익스트랙트 3g, 펩톤 10g, 소금 3g을 넣고, 온도 32-35℃, pH 7.0-7.4의 조건에서 상기의 균주를 접종배양하고, 1%의 대두박(大豆粕) 가수분해물과 극소량의 맥아당 및 질산 암모늄을 부잠사 정련액에 첨가한 후, 여기에 접종 배양을 주가(注加)하여 30-35℃, pH 7.0-7.4의 조건하에서 정련을 행하였다.5 liters of tap water was added to 1 kg of Bujasa, 3-4 hours of sericin extracted after treatment for 3-4 hours at 85-95 ℃, and 3g of beef and extract, 10g of peptone, and 3g of salt were added. Temperature 32-35 ℃, pH 7.0 The strain was inoculated and cultured under the conditions of -7.4, and 1% soybean meal hydrolysate and very small amounts of maltose and ammonium nitrate were added to the sub-silica refining solution, followed by inoculation culture. It refine | purified under the conditions of 30-35 degreeC, and pH 7.0-7.4.
실시예와 동일한 조건하에서 행한 자연부착균에 의한 발효와 본발명의 「배시러스ㆍ메거테리움 SY-7」균에 의한 발효정련결과를 비교하면 다음과 같다.The fermentation by spontaneous adherent bacteria under the same conditions as in Example and the fermentation refining results by the bacterium "Bacterium megaterium SY-7" of the present invention are as follows.
주(注) : (1) 속스렛(Soxhlet)장치로 추출 정량하였음.Note: (1) Extracted and quantified by Soxhlet apparatus.
단, 0=시료의 무수량(無水量)However, 0 = anhydrous amount of sample
01=유지(油脂) 추출후의 시료무수량0 1 = sample anhydrous amount after oil extraction
0p=유지 함유량0p = oil content
(2) KS-302(섬유의 인장강도 시험법)에 의거하여 Instrong's Texile Strength tester CR Type를 이용하여 측정하였음.(2) Measured using Instrong's Texile Strength tester CR Type in accordance with KS-302 (Fiber Tensile Strength Test Method).
(3) 자색계(紫色系) 형광등 밑에서 조사(照射)시키거나 염색결과로 판정하였음.(3) Irradiated under the purple fluorescent lamp or determined by the dyeing result.
(4) 마르세이유 비누 7%, 탄산소다 3%, 비이온 계면활성제 2ml/l의 용액에서 2.0-2.5시간 끓임.(4) Boil 2.0-2.5 hours in a solution of 7% Marseille soap, 3% sodium carbonate and 2 ml / l nonionic surfactant.
상기 표에서 보는 바와 같이 배시러스ㆍ메거테리움 SY-7균을 이용한 정련법이 종래의 일반적인 자연부착균에 의한 발효에 의해 생사를 정련하는 방법보다 우수함을 알 수가 있다.As shown in the above table, it can be seen that the refining method using Bacillus megaterium SY-7 bacteria is superior to the method of refining raw sand by fermentation by conventional common natural bacteria.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107723811A (en) * | 2017-11-02 | 2018-02-23 | 大连民族大学 | The unwinding method of degumming of the fermentation of bacillus method to tussah cocoon |
CN111606519A (en) * | 2020-06-09 | 2020-09-01 | 闫娟 | Advanced treatment method for electroplating wastewater |
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1980
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107723811A (en) * | 2017-11-02 | 2018-02-23 | 大连民族大学 | The unwinding method of degumming of the fermentation of bacillus method to tussah cocoon |
CN111606519A (en) * | 2020-06-09 | 2020-09-01 | 闫娟 | Advanced treatment method for electroplating wastewater |
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