• 한국식품과학회지
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• 제20권6호
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• pp.787-793
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• 1988

백포도주 양조시 페놀성분의 산화에 의한 갈변을 억제하여 색상과 풍미가 좋은 백포도주를 생산하고자 Golden Queen과 Neo-Muscat 및 Seibell-9110을 착즙전 또는 착즙후 아황산과 pectinase를 처리하여 과즙을 얻고 이를 $18{\sim}20^{\circ}C$에서 7-14일간 발효시켜 백포도주를 양조한 후 각 양조과정중 페놀류의 함량의 변화를 조사하고 양조한 백포도주에 polyclar AT(PVPP)를 처리한 후 열처리기간에 따른 갈변도의 변화를 측정하였다. 과즙중의 충 페놀함량은 파쇄한 과육에 아황산 pet-tinase 병행 처리구의 과즙이 무처리구보다 Golden Queen에서 33%, Neo-Muscat 70%, Seibell-9110에서 40% 더 높았고 청징도와 과즙 수율도 더 높았다. 백포도주의 일반성분은 품종별, 처리구간별 큰 차이가 없었으나 아황산 pectinase 병행 처리구의 메탄을 함량이 타구에 비하여 높았다. 또한 과즙에 비하여 백포도주의 총 페놀함량은 25-50%, 색도는 $50{\sim}80%$ 낮았다. PVPP 처리로 과즙중의 flavonoid phenol 함량은 $10{\sim}24%$, non-flavonoid phenol 함량은 약 3%가 제거되었다. 열처리 $(45^{\circ}C)$ 기간중 백포도주의 갈변은 Neo-Muscat과 Golden Queen의 경우 각 처리구에서 420nm의 흡광도가 0.3 이하로 심하지 않았으나 Seibell-9110의 경우 특히 파쇄한 과육에 아황산과 pectinase를 병행 처리한 구에서 심하게 갈변 하였다.

• 한국식품영양과학회지
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• 제40권9호
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• pp.1300-1306
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• 2011

미세한 입도분포와 전분 손상도를 최소화할 수 있는 쌀가루의 제분조건을 제시하고자 쌀 침지과정에서 pectinase와 cellulase 효소를 처리한 반습식제분 쌀가루의 이화학적 특성을 조사하였다. 효소처리는 단일효소 처리(0.05%)와 두 가지 효소를 동일비율로 사용한 복합효소처리로 0.05~0.2% 농도 수준에서 사용하였다. 입도분포는 복합효소처리(pectinase 0.05%+cellulase 0.05%) E에서 $53\;{\mu}m$ 이하의 입도분포율이 48.3%로 높아 가장 미세한 쌀가루를 얻을 수 있었다. 단백질 함량은 효소처리로 감소하였으며, 복합효소 처리 E에서 6.97%로 가장 낮았다. 손상전분 함량은 효소무처리구는 18.1%로 높은 반면 효소처리 후 감소하여 복합효소처리 E는 12.1%로 가장 낮았다. 효소처리로 겉보기 아밀로즈 함량, 물결합력, 용해도 및 팽윤력이 증가하였으며, 단일효소처리보다 복합효소처리에서 그 증가폭이 컸다. SEM 미세구조관찰에서 수침 및 효소처리를 통해 쌀가루의 집합체로부터 매끈하게 떨어져나간 미세입자의 증가를 확인할 수 있었다. 복합효소처리 쌀가루의 경우 RVA 호화특성인 최고점도, 냉각 점도, breakdown 및 total setback 점도의 증가를 보였다. 이상의 결과로 쌀가루 제분의 전처리 과정으로서 단일효소처리보다는 pectinase 0.05%와 cellulase 0.05%의 복합효소처리 침지조건이 높은 미세 입도분포율과 낮은 전분손상도를 갖는 쌀가루 제조에 가장 적합함을 알 수 있었으며 이는 호화특성에도 영향을 미쳐 쌀 가공품의 품질향상에 기여할 것으로 예상된다.

• 한국식품과학회지
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• 제37권4호
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• pp.574-578
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• 2005

복분자 발효주의 품질향상을 위하여 효모 종류 및 효소 등 처리방법을 달리하여 발효과정 중의 이화학적 특성을 검토한 결과 Saccharomyces cerevisiae KCCM 12224(Sc-24), 복분자 분리효모(Bok-3), 약주분리(Yak-7), Saccharomyces cerevisiae(Sc-24)와 약주효모(Yak-7) 혼합균주의 주발효 후 알코올 함량은 각각 11.08%, 10.62%, 10.18%, 10.26%이었으며, pectinase 첨가시 알코올 함량을 0.1-1.5% 증가시킬 수 있었다. 발효주의 유기산은 oxalic, citric, malic, shikimic, formic acid 등이었으며, 발효과정 중 citric acid와 malic acid가 큰 폭으로 감소되었다. 복분자주 발효 중 적정산도는 발효액 중의 citric acid의 함량변화에 의존적이었다. 복분자주의 색도는 발효초기에 유의적으로 감소되었으며 Sc-24, Yak-7 및 Bok-3+pectinase 처리구가 발효에 의한 색도의 변화가 비교적 낮았다. 이화학적 성분의 변화를 고려할 때 복분자주의 발효는 8-10일이 적당하였으며, Sc-24 및 Bok-3균주와 500ppm의 pectinase 첨가가 발효에 효과적이었다.

• 한국식생활문화학회지
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• 제11권5호
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• pp.683-687
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• 1996

Jujube paste was prepared by autoclaving the fresh jujube at 1.2 atm and $120^{\circ}C$ for 30 min and removing the skin and cores. In order to increase the juice yield, the paste was treated with pectinase, cellulase and their combinations. The soluble fractions of enzymatically treated jujube paste were characterized in terms of yield, pH, titratable acidity, color, Bx, transmittance and sugar compositions. The original paste exhibited the water soluble fraction of 57.3%. Of various quality factors, the clarity was the most significantly distinguished between pectinase and cellulase treatments. The cellulase treatment produced the cloudy juice with the yield of 83.60%. On the other hand, the clear juice was produced by the pectinase and combined treatments due to degradation of pectins, whose yields were 79.47% and 85.39%, respectively. The results clearly demonstrated that the pectinase treatments improved the solubilization efficiency and clarity.

• Journal of Microbiology and Biotechnology
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• 제21권2호
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• pp.192-196
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• 2011

Microbial induction of rusty-root was proved in this study. The enzymes hydrolyzing plant structural materials, including pectinase, pectolyase, ligninase, and cellulase, caused the rusty-root in ginseng. Pectinase and pectolyase produced the highest rusty-color formation. Ferrous ion ($Fe^{+++}$) caused the synergistic effect on rusty-root formation in ginseng when it was used with pectinase. The effect of ferric ion ($Fe^{++}$) on rusty-root formation was slow, compared with $Fe^{+++}$, probably due to gradual oxidation to $Fe^{+++}$. Other metal ions including the ferric ion ($Fe^{++}$) did not affect rusty-root formation. The endophytic bacteria Agrobacterium tumefaciens, Lysobacter gummosus, Pseudomonas veronii, Pseudomonas marginalis, Rhodococcus erythropolis, and Rhodococcus globerulus, and the rotten-root forming phytophathogenic fungus Cylindrocarpon destructans, caused rusty-root. The polyphenol formation (rusty color) was not significantly different between microorganisms. The rotten-root-forming C. destructans produced large quantities of external cellulase activity (${\approx}2.3$ U[${\mu}m$/min/mg protein]), which indicated the pathogenecity of the fungus, whereas the bacteria produced 0.1-0.7 U. The fungal external pectinase activities (0.05 U) and rusty-root formation activity were similar to those of the bacteria. In this report, we proved that microbial hydrolyzing enzymes caused rusty-root (Hue value $15^{\circ}$) of ginseng, and ferrous ion worsened the symptom.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2018년도 추계학술대회
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• pp.109-109
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• 2018

Bacillus subtilis B22, a chemotrophic and aerobic bacterial strain was isolated from homemade kimchi, identified by 16S rRNA gene sequencing. B22 was primarily screened by biochemical, carbon source utilization tests. B22 was used to produce pectinase and ${\beta}$-glucosidase by submerged fermentation under different light sources. B22 was incubated in pectin media and basal media (pH 7.0) under blue, green, red and white light-emitting diodes (LEDs), fluorescent white light, and in darkness at $37^{\circ}C$, orbital shaker 150 rpm for 24 hours. Fermentation under blue LEDs maximized pectinase production ($71.59{\pm}1.6U/mL$ at 24 h) and ${\beta}$-glucosidase production ($56.31{\pm}1.6U/mL$ at 24 h). Further, the production of enzyme increased to pectinase ($156{\pm}1.28U/mL$) and ${\beta}$-glucosidase ($172{\pm}1.28U/mL$) with 3% glucose as a carbon source. Activity and stability of the partially purified enzymes were higher at pH 6.0 to 8.0 and $25-55^{\circ}C$. The effect on the metal ions $Na^+$ and $K^+$ and (moderateactivity) $Mn^{2+}$ and $Ni^{2+}$ increased activity, while $Hg^{2+}$, $Cu^{2+}$, $Fe^{2+}$, and $Fe^{2+}$ inhibited activity. EDTA, phenylmethylsulfonyl fluoride and 5,5-dithiobis (2-nitrobenzoicacid) reduced activity, while tetrafluoroethylene and 1,10-phenanthroline inhibited activity. The amylase was highly tolerant of the surfactants TritonX-100, Tween-20, Tween-80 and compatible with organic solvents methanol, ethanol, isoamylalcohol, isopropanol, t-butylalcohol and the oxidizing agents hydrogen peroxide, sodium perborate and sodium hypochlorite, although potassium iodide and ammonium persulfate reduced activity. These properties suggest utility of pectinase and ${\beta}$-glucosidase produced by B. subtilis B22 under blue LED-mediated fermentation for industrial applications.

• 한국염색가공학회지
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• 제17권1호
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• pp.14-19
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• 2005

Study on the use of enzymes for textile wet processing has been very active. The exploratory research conducted herein is related to the bioscouring process for cotton fabric. The optimum concentration of alkaline pectinase(BioPrep) was in the range of 0.05～0.2 g/l, the proper treatment time was 30～60 minutes, the appropriate treatment temperature was $60^{\circ}C$ for both the batch method and the padding method. The simultaneous desizing/bioscouring by padding method did not give water absorbency as good as the bioscouring after desizing. Color of fabrics which were bioscoured and dyed with direct dyes and a reactive dye was just a little darker than that of NaOH scoured one. K/S and Lab values of the bioscoured fabrics, regardless of the degree of water absorbency, were quite similar to each other.

• The Plant Pathology Journal
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• 제23권4호
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• pp.233-238
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• 2007

Twenty five isolates of Sclerotinia sclerotiorum were recovered from different infested fields of vegetable along the heavily cultivated crops in Jordan valley. Cellulase and pectinase activities of those isolates were detected using CMC and pectin agar media, respectively. Diameter of the clearing zones on those media represented the level of such enzymatic activities, characteristic of each isolate. The virulence of those isolates was studied using a squash (Cucurbita pipo) cultivar under a greenhouse condition. The significance of correlating the enzymatic activity with the virulence of the isolates was ascertained and discussed.

• 한국식품저장유통학회지
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• 제3권2호
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• pp.179-185
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• 1996

This study was carried out for the purpose of improving the persimmon vinegar. Crushed persimmon(persimmon pulp) was used at alcohol fermentation using Saccharomyces bayanus for persimmon alcohol medium preparation. Glucose(8.39%) and fructose(7.96%) were the dominant free sugar in persimmon pulp before the at cohol fermentation. They decreased abruptly during alcohol fermentation and glucose was consumed more rapidly than fructose. Final alcohol concentration was finally reached to 8%(v/v) in 5 days for mentation of persimmon pulp. Pectinase pre-treatment of persimmon pulp resulted in tusker contents of galacturonic acid, galactose, methyl alcohol and isoamyl alcohol in main mash for alcohol fermentation than those in main mash prepared without pectinase pre-treatment. After alcohol fermentation tannin concentration was 350ppm and astringency was not perceived.

• Journal of Applied Biological Chemistry
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• 제57권2호
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• pp.137-140
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• 2014

A gene encoding thermostable pectinase (TmPec) was isolated from hyperthermophilic microorganism, Thermotoga maritima. The open reading frame (ORF) of TmPec gene is 1,104 bp long and encodes 367 amino acid residues with a molecular weight of 40,605 Da. To analyze the enzymatic activity and biochemical properties, the ORF of TmPec gene excluding putative signal sequence of 27 amino acids was introduced into the E. coli expression vector, pRSET-B, and overexpressed in E. coli BL21. Protein concentration of purified recombinant TmPec was 1.1 mg/mL with specific activity of 56 U/mg protein on pectin. The recombinant TmPec showed the highest activity at around $85-95^{\circ}C$, and at around pH 6.5. It was stable at temperature below $85^{\circ}C$. In the presence of $Ca^{2+}$, the activity of recombinant TmPec was increased to 146.3% of normal level. In contrast, $Ba^{2+}$ and Mn2+ showed strong inhibition to the recombinant TmPec.