• 한국미생물·생명공학회지
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• 제23권2호
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• pp.145-149
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• 1995

For the purpose of developing a new biodegradable detergent, we have isolated a gene encoding wide-range temperature applicable alkaline protease from Xanthomonas sp. YL-37 (Lee et al., 1994, Kor. J. Appl. Microbiol. Biotechnol.). An alkaline protease gene was isolated from the gene bank that was prepared from the chromosomal DNA of Xanthomonas sp. YL-37. From the results of agarose gel electrophoresis and a restriction enzyme mapping, a 2.7 kb DNA fragment containing the alkaline protease gene was inserted in the plasmid pUC9. Extracellular activity of a clone having alkaline protease gene was detected on SDS-polyacrylamide gel with activity staining assay. The molecular weight of alkaline protease was determined to be about 64 kDa from 11% SDS-PAGE analysis. Alkaline protease activity, produced from E. coli which harboring the plasmid, showed no difference at reaction temperature 20, 30 and 40$\circ$C, respectively. This result showed that alkaline protease produced from E. coli harboring the plasmid was apparently the same as that of Xanthomonas sp. YL-37.

• Applied Biological Chemistry
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• 제38권5호
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• pp.376-381
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• 1995

내열성 alkaline phosphatase의 탐색을 위해 극도호열균중에서 Thermus caldophilus GK24 균주를 선정하였다. 이 균주를 이용하여 basal salts에 sodium glutamate, bactotryptone, glucose 및 yeast extract를 첨가시킨 배지에서 alkaline phosphatase 생산을 검토하였다. 그 결과 sodium glutamate가 alkaline phosphatase 유도에 효과적인 것으로 판명되었다. Alkaline phosphatase 생산을 위한 최적유도용 배지는 basal salts에 0.3% sodium glutamate, 0.2% bactotryptone, 0.5% glucose를 첨가한 것으로 효소활성은 기본배지보다 약 6배, 표준배지 보다는 약 27.5배 증가하였다. T. caldophilus GK24 alkaline phosphatase는 유도효소로 판명되었다. 무기인산 결핍시에 효소가 생산되며, 생육배지에 무기인산을 첨가하면 효소합성에 저해효과가 있었다.

• 한국동물학회지
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• 제17권4호
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• pp.167-176
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• 1974

著者들은 3種의 어류를 재료로 하여, 咽頭, 食道, 胃, 前場部 및 後場部 alkaline phosphatase의 分布상태를 비교관찰하여 다음과 같은 결과를 얻었다. 1. 미꾸리, 가물치의 咽頭上皮 細胞層에서 중등도의 alkaline phosphatase 양성반응을, 미꾸리와 뱀장어의 食道上皮의 基底細胞層에 증등도의 양성반응을 보였다. 2. 上記 全 魚類의 咽頭, 食道, 腸管膨大部 및 腸粘膜의 杯狀細胞와 胃腺細胞에서는 alkaline phosphatase 활성은 관찰할 수 없었다. 3. 腸管膨大部 및 腸上皮 유리연에 강한 alkaline phosphatase 양성반응을 관찰할 수 있었으나, 미꾸리의 後場部의 上皮유리연에서는 미약한 반응을 보였다.

• 한국의류산업학회지
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• 제7권1호
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• pp.85-90
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• 2005

The effect of sodium acetate to reduce the fiber damage and hardening of acetate fabrics during alkaline treatment is studied. The optimal condition is controlled concentration 2%, at $50^{\circ}C$ for 6 minutes and at $70^{\circ}C$ for 2 minutes through the result of weight loss, shrinkage and tensile strength. Alkaline treated acetate fabrics under optimal condition show softer than untreated acetate fabrics. Alkaline treatment with sodium acetate brings the reduction in hardening and shrinkage in internal fiber of acetate fabric. Also, alkaline treatment with sodium acetate improves the tensile strength of acetate fabrics compared with only alkaline treatment. The moisture regain of acetate fabrics is also improved by alkaline treatment under optimal condition.

• 한국염색가공학회지
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• 제13권1호
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• pp.9-17
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• 2001

The purpose of this study is to present basic data for the enzymatic modification of acetate fabrics. The weight loss and rate of weight loss of acetate fabrics increased with increasing NaOH concentration and treating time. Acetyl value decreased as the weight loss became higher. The weight loss of alkaline-treated acetate fabrics were directly proportional to the concentration and treating time of cellulase. The optimum temperature and pH in cellulase treatment were $55^\circ{C}$ and pH 3.5. The surface shape revealed that density of fiber decreased by alkaline-treatment. With the treating time of cellulase, fibrillation occurred. In case of higher weight loss in alkaline treatment, fibril is removed after 180 min. The tensile strength decreased by alkaline and cellulase treatment. Especially, in case of higher weight loss of alkaline treatment, tensile strength decreased suddenly. Alkaline treatment increased the drapability of acetates, while cellulase treatment increased it initially but decreased gradually with treatment time. The dyeability after alkaline treatment was improved for reactive dye, but deteriorated for disperse dye. The cellulase treatment of acetate lowered the dyeability for both types of dyes.

• 한국동물학회지
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• 제17권4호
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• pp.177-184
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• 1974

발생중의 무당개구리에서의 전신 및 중신 alkaline phosphatase 활성을 Gomori 변법을 써서 관찰하였다. 전신 분비세관의 분화와 함께 세관 刷子綠에 출현한 alkaline phosphataseghkf성은 　蓋완성기에 최고도에 달하였다가 제3후지 형성기에 전신의 퇴화와 함께 효소활성은 감소 소실되었다. 　蓋완성기에 출현한 중신세관에서의 alkaline phosphatase 활성은 변태기를 통하여 강한 양성반응을 보였다.

• 한국응용곤충학회지
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• 제27권4호
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• pp.211-218
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• 1988

담배거세미나방(Spodoptera litura: SI), 누에(Bombyx mori: Bm) 및 흰불나방(Hyphantria cunea : Hc)으로부터 분리된 핵다각체병 바이러스(nuclear polyhedrosis virus : NPV)의 다각체의 단백질의 특성과 그에 대한 alkaline protease의 영향을 SDS-PAGE 및 혈정학적 방법으로 분석했다. Alkaline protease를 부활화시킨 후 다가체 단백질을 SDS-PAGE한 결과, BmNPV의 경우 30kD, SINPV와 HcNPV는 31kD의 단일 major band 및 이것들의 종합체(polymer)인 57kD와 66kD의 minor band들이 관찰되었다. Alkaline protease의 부활화를 성략한 SI NPV 다각체를 알칼리 용액으로 시간 차이를 두고 처리한 후 SDS-PAGE한 결고, 알칼리 처리시간이 경과함에 따라서 alkaline protease활성에 의해 다각체 단백질이 일정한 pattern으로 저분자화됨이 뚜렷하였다. SINPV 와 BmNPV 다각체 단백질의 항체를 제조하여 SINPV, BmNPV및 HcNPV 다각체 단백질간의 혈정학적 상동성을 이중형역광산법과 Western blot으로 비교한 결과는 3종 모두에서 공통 antigenic determinants의 존재가 인정되었으며 major 다각체 단백질의 종합체 형성과 alkaline protease에 의한 분해를 확인했다.

• 유기물자원화
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• 제6권1호
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• pp.1-12
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• 1998

피혁제조시 발생되는 크롬을 함유한 피혁 고형폐기물인 shaving scrap의 단백질 자원화 가능성을 검토하기 위하여 MgO를 기본으로 하여 alkaline inducing agents 및 alkaline proteolytic enzymes을 혼용처리하여 shaving scrap으로 부터 회수한 가수분해 단백질의 용해도, 무기성분 함량, 분자량분포 등을 비교 검토함으로서 최적 가수분해 조건 및 액체비료의 원료로 활용하기 위한 저분자 단백질의 회수방안을 조사한 결과는 다음과 같다. Alkaline inducing agents의 혼용처리에 의한 shaving scrap의 가수분해 실험결과 7% MgO를 기본으로 하여 alkaline inducing agents 종류에 따라 65~85% 범위로 용해도 차이가 뚜렷하였으며, 가수분해되는 정도는 NaOH>$Ca(OH)_2$>KOH순으로 나타났으며, 획득된 hydrolyzed protein의 평균분자량은 NaOH처리시 약 10 KD, $Ca(OH)_2$ 처리시 약 40 KD, KOH처리시 약 80 KD이었으며, 크롬함유량은 약 15 ppm이었다. Alkaline proteolytic enzymes의 혼용처리에 의한 shaving scrap의 가수분해 실험결과 alkaline proteolytic enzymes 종류에 따라 Alcalase>Esperase>Savinase순으로 용해도 차이를 보였으며, 0.5% Alcalase의 처리에 의해 용해도 85%수준, 평균분자량 1 KD 미만, 크롬 함유량 10ppm 이하인 저분자 형태의 hydrolyzed protein을 획득할 수 있었다.

• 펄프종이기술
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• 제48권2호
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• pp.56-60
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• 2016

Neutral or alkaline papermaking provides many advantages in paper strength and processing conditions. It also provides the opportunity of using calcium carbonate fillers in papermaking. These diverse advantages have made almost all paper machines of printing and writing papers run under neutral and alkaline conditions. On the other hand, linerboard machines, which use recycled papers as a raw material, are running under acid conditions using a rosin sizing system. Because the recycled raw materials used by the linerboard industry contain significant amounts of alkaline papers, the linerboard industry has an interest in the possibility of using the neutral or alkaline papermaking opportunity. In this study, the compatibility of the recycled linerboards under neutral or alkaline papermaking conditions was examined by recycling them under various pH conditions. The sizing degree of the papers recycled under neutral or alkaline was significantly lower than that of acid formed papers indicating that during the neutral or alkaline recycling process the rosin sized papers lost their sizing efficiency. Recycling of acid formed linerboards under neutral or alkaline conditions increased the amount of foam, and the foam contained substantial amount of solid materials derived from the acid sizing systems. Use of cationic polyelectrolytes including PEI and poly-DADMAC improved the sizing degree of the recycled papers under neutral and alkaline conditions. PEI decreased the foam generation as well while poly-DADMAC did not show any reducing effect of the foam. These results suggest that PEI forms coordinate bonds with rosin acid and precipitate them onto the surface of recycled fibers, while the reaction products between poly-DADMAC and rosin acid ions still remain water soluble under neutral or alkaline conditions.

• 한국미생물·생명공학회지
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• 제23권5호
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• pp.544-549
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• 1995

The alkaline elastase is an extracellular serine protease of the alkalophilic Bacillus strain Ya-B. To increase the gene copy number and the production level of the alkaline elastase Ya-B, we designed, on the B. subtilis chromosome, a gene amplification of the 10.6 kb repeating unit containing amyE, aleE (alkaline elastase Ya-B gene) and tmrB. The aleE was inserted between amyE and tmrB, and B. subtilis APT119 strain was transformed with this amyE-aleE-tmrB-junction region fragment. As a result, we succeeded in obtaining tunicamycin-resistant (Tm$^{r}$) transformants (Tf-1, Tf-2) in which the designed gene amplification of 10.6 kb occurred in chromosome. The transformants showed high productivity of $\alpha $-amylase and alkaline elastase Ya-B. The copy number of the repeating unit (amyE-aleE-tmrB) was estimated to be 25, but plasmid vector (pUC19) was not integrated. The amplified aleE of chromosome was more stable than that of plasmid in absence of antibiotics.