• Applied Biological Chemistry
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• 제4권
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• pp.17-22
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• 1963

원료배합(原料配合)을 다리한 간장용(用) 고일(一)지의 제국중(製麴中)에 있어서와 건조(乾燥)고일(一)지의 각종효소(各種酵素) activity 및 성분(成分)의 변화(變化)를 측정(測定)하여 다음결과(結果)를 얻었다. 1. 건조(乾燥)고일(一)지는 중성부근(中性附近)(pH 6.0)에 활성(活性)을 갖는 Protease가 주체(主體)를 이루며 산성(酸性) 및 alkali성측(性側)의 Protease activity는 이보다 미약(微弱)하고 밀을 많이 배합(配合)한 구(區)일수록 산성(酸性) 및 중성측(中性側) Protease activity가 높아지는 반면(反面)에 alkali성측(性側)은 이와 반대(反對)되는 경향(傾向)을 보였다. 2. 제국중(製麴中) 각종효소(各種酵素) activity는 모두 증가(增加)되었고 밀이 많은 배합구(配合區)일수록 ${\alpha}-Amylase$는 그 activity가 높아졌다. 3. 제국중(製麴中) 전당(全糖)은 감소(減少)되었으나 직당(直糖) 및 아미노 태질소(態窒素)와 전질소(全窒素)는 증가(增加)되었다. 4. 건조(乾燥)고일(一)지에 있어서 밀이 많은 배합구(配合區)일수록 직당(直糖) 및 전당(全糖)의 함량(含量)이 많어졌으나 전질소(全窒素)는 적어졌고 아미노(態窒素)는 차이(差異)가 없었다.

• 한국미생물·생명공학회지
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• 제19권3호
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• pp.290-295
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• 1991

Maltose 생산효소인 Fungamyl과 생전분의 알칼리성 현탁액에 고형분쇄마찰매체를 첨가교반하면서 증자액화과정을 거치지 않고 생전분으로부터 maltose를 직접 생성시키는 연구를 수행하였다. 불용성 생전분을 기질로 하는 분쇄마찰 효소반응계에서 효소반응은 증자액화된 전분을 기질로 하는 기종의 maltose 제조법과 비슷한 효소반응속도를 보였다. 그러나 24시간후 maltose 농도는 증자법을 초과하여, 생전분의 농도가 150g/l일 때 95g/l의 maltose를 얻을 수 있었고, 첨가생전분에 대한 수율은 0.60이었다. 또한 생산된 포도당, maltose, maltoriose의 농도는 각각 20, 95 그리고 13g/l였으며, maltose의 함량은 72%로서 증자법의 6%0에 비하여 매우 높았다.

• 환경위생공학
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• 제24권1호
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• pp.40-46
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• 2009

The enzyme expressed from strain L-49 was 2.01 times higher than that of original strain. Strain L-49 can grow on culture plate with $50{\mu}g/mL$ ampicillin. The synthesis of $\alpha$-amylase was greatly suppressed when strain L-49 was grown on monosaccharide such as glucose and polysaccharide at the same time cell concentration was low. Amylase production was enhanced when the bacterium was grown on starch and dextrin. Among different nitrogen sources tried, yeast extract was found to be the best followed by panpeptone, peptone, meat extract, bean meal, and corn steep liquor. The average rate of enzyme production was enhanced for 3~4 times in fermentation time from 24h to 44h. The sugar uptake rate has also increased. Low oxygen supply rate enhanced the rate of strain propagation but depressed the enzyme production. Hence it is benefit to obtain high enzyme activity that agitation speed maintained not lower than 400r/min and aeration rate maintained greater than 1:1vvm.

• 한국식품과학회지
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• 제27권1호
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• pp.56-62
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• 1995

This study was designed to investigate the changes in microflora and enzyme activities of traditional kochujang meju during fermentation for 60 days. The pH of meju decreased continously up to 40 days of aging and then increased slightly thereafter, while the change in titratable acidity showed the opposite trend to that of pH. The viable cell count of aerobic bacteria increared gradually for up to 40 days of fermentation and then decreased slightly thereafter, while that of molds and yeasts showed a rapid increase up to 40 days of fermentation and then leveled off. ${\alpha}-amylase$ activity increased slightly for up to 40 days of meju fermentation and then stabilized. On the other hand, ${\beta}-amylase$ and glucoamylase activities did not show a significant change for up to 20 days of fermentation and then increased rapidly at 40th day of fermentation. Acidic, neutral and alkaline protease activities increased sharply up to 40 days of aging and then decreased significently at 60th day of fermentation. These results suggest that meju fermented for 40 days had the highest quality in terms of the number of microflora and enzyme activity.

• Journal of Plant Biology
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• 제35권4호
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• pp.333-338
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• 1992

다양한 발달단계에 있는 은행종자의 자성배우체, 자엽 및 유근에서 탄수화물의 함량과 여러 가수분해효소(아밀라제, 인버타제 및 인산가수분해효소)의 활성을 비교하였다. 종자의 초기발아시에 아밀라제의 활성이 크게 증가함에 따라 자성배우체의 전분이 현저한 감소를 보인 반면 수용성 당들은 증가하였다. 인버타제의 활성은 건조한 종자에서는 매우 낮았으며 바라된 자엽과 유근에서 점진적으로 증가하였다. 인산가수분해효소의 활성은 유근이 신장되는 단계에서 변화를 나타내었으며 산성-인산가수분해효소가 알카리성-인산가수분해효소보다 더 높은 활성을 보였다.

• Journal of Ginseng Research
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• 제14권1호
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• pp.21-26
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• 1990

The chemical composition and stabilities of the purified ginseng invertase were investigated. The purified enzyme was found to be a glycoprotein composed of 80.2% protein and 19.7% total sugar. The protein component of the enzyme was composed of acidic amino acid (9.3%), basic amino acid (48.9%), nonpolar amino acid (21.4%), polar amino acid (20.4%) and 6.1% S-containing amino acid. It showed especially high contents of histidine and serine. The enzyme was inactivated almost completely by the treatment with some proteases (papain, pepsin. trypsin, pancreatin and microbial alkaline pretense) and protein denatllrants (8M urea and 6M guanidine-HC1), bolt not with glyrosidase (${\alpha}$-amylase, ${\beta}$-amylase. glcoamylese and cellullase). btonosaccharides sllch as glilrose, fructose, galactose and mannose did not exert any influence on the enzyme activity. The activity of the enzyme was inhibited by Ag+, Mn2+, Hg2+, Zn2+ and Al3+, whereas Ca2+, Mg2+, Ba2+ and Fe3+ gave rather activating effects on the enzyme activity. The enzyme was relatively stable in the VH range of VH 6 and 8, and at the temperatures below 35$^{\circ}C$.

• 미생물학회지
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• 제18권2호
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• pp.51-58
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• 1980

Mutational experiments were performed to improved to improve the protease productivity of Aspergillus flavus KU 153, which is selected among the wild strains. A UV-induced mutant strain having high protease productivity was obtained by the use of the clear zone method as a simple criterion for a primary screening test. Neutral and alkaline protease activities of hte mutant strain were higher than 1.8 times, comopared with those of the parental strain, respectively, while in the case of acid protease, it was 2.7 times. The mutant strain selected was more powerful in the production of cellulase and amylase, as well s protease in wheat bran, compared with those of the parental strain. protease production of the parental strain has reached maximum level at 3 days culture, while alkaline nad neutral protease production of the mutantstrain has reached at 2 days culture. On the other hand, the mutant strain formed the spore slowly, compared with the parental strain. Column chromatography of the neutral protease on DEAE-Sephadex A-50 showed that the mutant strain was not induced the formation of another neutral protease isozyme, but induced the variation in the function of regulatory gene.

• Journal of Life Science
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• 제11권1호
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• pp.14-21
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• 2001

To investigate the changes of carbohydrate metabolism in the senescing leaves of Zea mays during dark-induced senescence, the changes in the contents of reducing sugar, sucrose and starch as well as the activities of sucrose synthase, three isozymes of invertase, and ${\alpha}$-amylase were measured. In the senescing leaves, the content of reducing sugars temporarily increased at 4 d and rapidly decreased thereafter, whereas sucrose contents gradually decreased thereafter, whereas sucrose contents gradually decreased until 3 d of senscence and significantly decreased thereafter. The activities of intracellular invertases such as soluble acid and alkaline formed gradually enhanced until 4 d of leaf senescence and significantly declined thereafter. The extracellular invertase activity showed no significant changes during leaf senescence. The deactivation of sucrose synthase was observed within 3 d of leaf senscence. On the other hand, the starch contents gradually declined during 2 d of leaf senescence, and showed a temporary increase at 3 d, which is similar to the pattern of sucrose synthase activity., These results imply that sucrose in the senescing leaves. The major enzymes which correlated to the breakdown of sucrose during dark-induced senescence were soluble acid and alkaline invertases, not sucrose and ABA accelerated leaf senescence by inducing the accumulation of reducing sugar. These result, therefore, that leaf senescence may be mediated by the temporary quantitative changes of reducing sugar induced by the activation of intracellualr inveertases.

• 대한골관절종양학회지
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• 제7권2호
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• pp.41-50
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• 2001

목적 : 골육종 환자의 조직과 혈청에서 DNase, RNase, 5'-nucleotidase, alkaline phosphatase 및 amylase 활성도를 측정하여 그 활성도의 변동을 보았고 이들 효소가 골육종의 표지자로 이용될 수 있는지 알아보았다. 대상 및 연구방법 : 골육종 환자의 혈청과 종양조직은 1 2예로부터 얻었으며, 이에 대한 대조조직은 동일 환자의 정상부위에서 채취하였다. 조직 추출액을 얻어서 핵산, 단백함량, 그리고 효소 활성도의 측정에 사용하였다. DEAE-cellulose chromatography에 의해 골육종 조직의 acid DNase, neutral RNase, RNase inhibitor와 단백을 분리하고 그활성도와 단백 함량을 측정하였다. 결과 : 골육종 조직의 acid DNase, RNase, 5'-nucleotidase, alkaline phosphatase 활성도는 유의하게 상승하였고, 효소활성도의 양성율도 높게 나타났다. neutral RNase의 활성도가 특히 높았으며, RNase inhibitor는 neutral RNase와 복합을 이루면서 그 활성도가 유의하게 증가하였다. 혈청 neutral RNase 활성도가 유의하게 상승하였다. DEAE-cellulose column chromatography에 의해 acid DNase는 단일효소로서, 그리고 neutral RNase는 5개의 isozyme으로 분리되었다. 결론 : 이들 효소의 병용이 골육종의 생화학적 표지자로서 이용될 수 있을 가능성을 시사하였다. 또한 혈청 neutral RNase활성도의 측정이 골육종의 생화학적 표지자로서의 역할을 시사하였다. acid DNase와 neutral RNase가 골육종의 발생과 억제과정에 작용하고 있을 가능성을 시사하였다.

• Advances in Traditional Medicine
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• 제6권3호
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• pp.186-195
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• 2006

The present study was carried out to determine the involvement of opioid and non-opioid receptor and the effect of pH and enzymes on the recently reported antinociceptive activity of aqueous extract of Corchorus olitorius (AECO) leaves using the abdominal constriction test. The extract was prepared by soaking the dried powdered leaves of Corchorus (C.) olitorius in distilled water overnight, and the supernatant obtained was considered as a stock solution with 100% concentration/ strength. The extract, administered subcutaneously in the concentrations/ strength of 10, 50 and 100%, was found to show a significant concentration-independent antinociception. The 50% concentration AECO were further used to study on the above mentioned parameters. The extract exhibited: significant (P < 0.05) decreased in activity when pre-treated (s.c.) against 10 mg/kg naloxonazine, bicuculine (10 mg/kg), phenoxybenzamine (10 mg/kg), 10 mg/kg pindolol, and 5 mg/kg mecamylamme, but not 10 mg/kg naltrindole, 10 mg/kg atropine, respectively; significant (P < 0.05) decreased in activity after pre-treatment against 10% a-amylase, but not 1 % protease or 10% lipase and; significant (P < 0.05) decreased in activity after exposure to alkaline condition (pH between 9 and 13) while maintaining the activity at acidic condition, respectively. The C. olitorius leaves antinociception, which involved, at least in part, activation of $\mu-opioid,\;\alpha-and\;\beta-adrenergic$, and nicotinic receptors, was found to decrease under alkaline condition and in the presence of $\alpha-amylase$.