• Current Research on Agriculture and Life Sciences
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• 제17권
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• pp.45-52
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• 1999

하수슬러지의 퇴비화를 촉진할 수 있는 방안을 검토하기 위하여 2월 및 8월에 하수슬러지를 채취하여 생균수를 측정한 결과 하수종말처리장에서의 폐수처리시 유입수량 변동, 양이온성 polyacrylamide의 사용량 및 기후 변동을 포함하는 여러 조건의 변화에 따라 미생물 종과 미생물수의 변동이 많았으며, 미소후생동물의 종류 및 활동성도 계절에 따른 차이가 있었다. 양이온성 polyacrylamide가 미생물 생육에 미치는 영향을 조사한 결과 양이온성 polyacrylamide의 농도가 0.8% 이상일 때는 모든 균주의 생육이 저해되었으나 0.2% 이하에서는 균 생육에 지장을 초래하지 않았다. 하수슬러지의 퇴비화 과정중에 관여하는 미생물의 균종과 균수를 조사하고자 하였으나 미생물의 생태적 생리적 특성과 퇴비화의 일정한 상관관계를 도출할 수는 없었다. 그러나 유기물 함량과 bulking agent로 톱밥을 투여하였을 경우 미생물의 균종과 균수의 증가가 관찰되었다. 하수종말처리장의 폭기조 투입직전 활성슬러지, 폭기조내 활성슬러지, 하수슬러지와 bulking agent로 톱밥을 혼합처리하여 관찰한 결과 Fragilaria sp., Proales sp., Vorticella sp., Schizothrix sp., Anabaena sp., Zoothaminium sp., Epstylis sp., Arcella sp., Balantidium sp., Actinophrys sp., Synedra sp., Euglypha sp., Ulothrix sp., Anacystis sp., 및 Clostium sp. 등의 다양한 미소 후생동물이 관찰되었다. 특히 전기간에 걸쳐 Fragilaria sp., Proales sp., Vorticella sp. 몇 Schizothrix sp.가 관찰되었다. 슬러지 내에 존재하는 세균, 효모, 방선균, 곰팡이, 미세조류, 원생동물 및 하등동물은 하수슬러지의 퇴비화 또는 감량화 과정 중에 존재하여 공극의 확보와 같은 물리적인 퇴비화 촉진과 생물학적 분해작용에 의한 퇴비화 촉진 효과를 얻을 수 있을 것이다.

• 한국환경보건학회지
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• 제24권2호
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• pp.104-109
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• 1998

The objective of this study was to examine the effect of polymer coating on the initial microorganism attachment and the biofilm growth. Such as nonion(polyacrylamine), anion(CMC-Na) and cation polymer coagulant(chitosan and PEI) were used for coating material of the support carrier(acryl plate). When polymer coagulant was coated with 5, 10, 20, 35, 50, 100 and 200 mg/l on the surface of acryl plate, initial microorganism attachment increased and optimum concentration for the attachment was 35 mg/l. Biofilm growth experiments were conducted with the substrate loading of 12.7gSCOD/$m^2\cdot$ day using RBC. The polymer coagulants such as CMC-Na, polyacrylamide, PEI and chitosan coating on the acryl plate facilitated the biofilm growth of microorganisms. Until the biofilm dry weight grows up to 0. 0038g/cm$^2$, biofilm growth on the plate coated with cation polymer like chitosan was better than that on the coated plate of nonion(polyacrylamine), anion(CMC-Na) polymer coagulant.

• Journal of Plant Biology
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• 제33권4호
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• pp.293-301
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• 1990

We have purified and characterized a deoxyribonuclease from zygotes of the eukaryotic green alga, Chlamydomonas reinhardtii and investigated effects of the polyamines, putrescine, spermidine and spermine on the purifed endonuclease-catalyzed cleavage of plasmid DNA. The enzyme has a molecular weight of about 37 kDa as measured by gel filtration and SDS-polyacrylamide gel electrophoresis. There is no requirement for a divalent cation. The activity is sensitive to ionic strength, as NaCl and KCl result in inhibition. The cleavage of plasmid DNA by the purified endonuclease was effectively inhibited by polyamines. The enzyme activity was inhibited more effectively by spermine than by spermidine. The inhibition by putrescine was lower than the other two polyamines.

• 생물환경조절학회지
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• 제14권3호
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• pp.196-202
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• 2005

본 연구는 상토의 보수성 증가를 위하여 혼합되는 acrylamide 계통 고흡수성 수지인 Stocksorb C(STSB)의 수분 흡수 특성, 수분 흡수에 영향을 미치는 각종 무기염의 종류 및 농도, STSB가 침지된 외부용액속의 무기염 농도 변화를 구명하고자 수행하였다. STSB의 수분 흡수량은 증류수에 침지한 경우 약 180 $mL{\cdot}g^{-1}$였다. 1가의 양이온을 포함한 염인 $KH_2PO_4,\;KNO_3$ 또는 $(NH_4)_2SO_4$를 용해시킨 용액의 농도가 높아질수록 흡수량이 저하되었으나 세 종류 양이온의 종류에 따른 차이는 크지 않았다. $Ca(NO_3)_2{\cdot}4H_2O$ 다양한 농도로 용해시킨 용액 속에 STSB를 침지시킨 경우 수분흡수능 저하가 심하여 20 $meq{\cdot}L^{-1}Ca(NO_3)_2{\cdot}4H_2O$ 용액에서 약 25 $mL{\cdot}g^{-1}$ 수분을 흡수하였다. $Mg(NO_3)_2{\cdot}6H_2O$나 $MgSO_4{\cdot}7H_2O$를 용해시킨 용액의 농도가 높아질수록 수분 흡수량이 심하게 저하하였고, 1가의 양이온이 포함된 염을 용해시킨 용액에서보다 그 정도가 심하였다. 그러나 요소의 농도를 증가시킨 용액에서의 수분 흡수량은 저하되지 않았다. 침지전 Hoagland용액의 농도가 높거나, 침지시간이 길어질수록 STSB를 침지시킨 용액에서의 $K^+$및 $NH_4^+-N$의 농도가 점차 높아졌다. Hoagland 용액의 희석배수와 무관하게 침지시간이 길어질수록 외부용액의 $NO_3^--N,\;H_2PO_4^-$ 및 $SO_4^{-2}$ 농도가 약간 상승하였고, 24시간 경과 후 각각 5,300, 250 및 1,500 $mg{\cdot}L^{-1}$ 농도로 분석되었다.

• 한국동물학회지
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• 제22권4호
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• pp.141-152
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• 1979

고양이 백혈병 바이러스에서 reverse transcriptase를 분리하여 생화학적 및 면역학적 연구를 하였다. 분자량은 72,000이고, DNA polymerase와 RNase H의 활성은 0.05-1 mM $M_n^2+$와 50-80 mM KCl에서 가장 좋았다. DNA polymerase와 RNase H는 같은 단백질 분자에 있으며, chymotrypsin 처리로서 RNase H를 쪼개낼 수 있으며, 이 RNase H도 reverse transcriptase의 항체에 의해서 활성이 거의 억제 된다. Reverse transcriptase의 항체 결합위치와 활성을 내는 위치는 다른 것 같다.

• Applied Biological Chemistry
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• 제46권3호
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• pp.176-182
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• 2003

한국재래간장으로부터 혈전용해효소를 강하게 생산하는 균주를 선발하고 이를 Bacillus subtilis K7로 동정하였다. B. subtilis K7이 생산하는 혈전용해성 protease를 정제하여 분자량을 확인한 결과 21,500 Da이었다. 정제된 효소의 최적반응조건은 $40^{\circ}C$와 pH 9.0이었으며 pH 5.0라서 12.0까지 안정하고 $50^{\circ}C$에서 20분간 열처리한 후에도 50%이상의 효소활성을 가지며 EDTA, CDTA 및 iodoacetat에 실활하는 효소이었다. 이 효소의 fibrin에 대한 Km 값은 $1.8{\times}10^{-2}$ M이었다.

• 한국건축시공학회지
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• 제2권3호
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• pp.131-138
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• 2002

The objective of the study is to examine the characteristic correlations between reinforcing carbon fiber and interfacial adhesion agent since the interfacial adhesion strength between reinforcing carbon fiber and matrices is believed to be an essential element influencing the physical properties in carbon fiber reinforced cement composite using slurry method. The integrity of interfacial adhesion between reinforcing fiber and cement not only affects the quality of fiber reinforced cement composite but also influences to a large degree the physical properties of the cement composite when producing carbon fiber reinforced cement composite using slurry method. Having analyzed the physical properties 1.e., water content, tensile strength, flexural strength and flexural toughness of carbon fiber reinforced cement composite specimens, C-PAM(cation polyacrylamide) was determined to be an optimum interfacial adhesion agent. The study has also demonstrated that interfacial adhesion strength varies largely on the content and type of the reinforcing fiber. Judging from magnified view of the tensile shear cross-section using VMS(video microscope system), interfacial adhesion strength between reinforcing fiber and matrices is affected by the type of interfacial adhesion agent. According to the result of the experiments, C-PAM was determined to be an ideal interfacial adhesion agent when using carbon fiber in producing carbon fiber reinforced cement composite with the optimum content of carbon fiber being established.

• Preventive Nutrition and Food Science
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• 제7권1호
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• pp.43-47
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• 2002

Crude caseinomacropeptide (CMP) was prepared from Na-caseinate using a commercial renneting enzyme. Most of the crude CMP was released from the Na-caseinate by hydrolyzing with the enzyme for 40 min. The hydrolysis of the k-casein with carbohydrate was slower than that of the k-casein without carbohydrate, as shown by the analyses of the sialic acid content and the tricine-SDS-polyacrylamide gel electrophoresis. The yield of crude CMP from Na-caseinate was 3.7%. Cation exchange chromatography showed that the crude CMP consisted of 40.5% CMP and 59.5% caseinogylcomacropetide (CGP). The effect of the TCA concentration on the solubility of CMP and CGP was determined by using crude CMP. The amounts of crude CMP and sialic acid decreased in the proportion to the increase of trichloroacetic acid (TCA) concentration from 2 to 12%, suggesting that the CGP containing carbohydrate, as well as the CMP having no carbohydrate, was precipitated in a range of 4 to 12%, depending on the TCA concentration. This result supports the hypothesis that the different non-glycosylated and glycosylated forms of CMP have different sensitivities to TCA precipitation.

• Bulletin of the Korean Chemical Society
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• 제15권9호
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• pp.719-724
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• 1994

Major cellulase components, such as three endoglucanases (endoglucanases I, II, and III) and one exoglucanase (exoglucanase II), were isolated from a commercial cellulase (Meicelase TP 60) derived from the fungus Trichoderma viride by a series of chromatography procedures. These procedures were the gel filtration on Bio-Gel, the anion exchange on DEAE-Bio-Gel A, the cation exchange on SP-Sephadex C50, and the affinity chromatography on Avicel cellulose. The average molecular weights determined by SDS-polyacrylamide gel electrophoretic analysis were 51,000, 59,000, 41,000 and 62,000 Da for endoglucanases I, II and III and exoglucanase II, respectively. The extinction coefficients, ${\varepsilon}^{1%}$ 280 nm, of these enzymes were 11.7, 3.3, 7.2 and 11.3, respectively. Among them, the endoglucanase II showed the very low value of the coefficient compared with the others. On the other hand, it was found that endoglucanase II and III were of more random hydrolytic mode on carboxymethylcellulose as compared with those of endoglucanase I and exoglucanase II. Especially, endoglucanase I showed less random action than that of exoglucanase II. In the hydrolysis of insoluble cellulose by the enzyme components, cellobiose was the major product, but glucose was the major product by endoglucanase III.

• 대한수의학회지
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• 제36권2호
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• pp.379-387
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• 1996

The objects of the present study were to establish the method of purification, subunit dissociation of verotoxin-2 (VT2) produced by Escherichia coli O157:H7, and to investigate the characteristics of purified verotoxin-2 such as molecular weight and composition of amino acid. The results were summerized as follows; Verotoxin-2 was extracted by addition of polymyxin B sulfate into bacterial cell lysate prepared from Escherichia coli O157:H7(KSC109). As an initial step, the bacterial cell lysate was precipitated with 30% saturated ammonium sulfate. The precipitated crude toxin was then subjected to anion-exchange, chromatofocusing and cation-exchange chromatography. Using this scheme, we obtained highly purified toxin with a specific activity of $1.1{\times}10^9$ $CD_{50}/mg$. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis(SDS-PAGE) for purified VT2 showed two protein bands. The upper band, approximately 32 Kd, was supposed as A subunit and the lower band, approximately 7.7 Kd, was supposed as B subunit. When the toxin was separated in the subunit-dissociating solution, two peaks emerged with retention times of 15 and 28 min by HPLC. These peaks represented A subunit and B subunit, respectively. The amino acid composition of purified VT2 were made up in order of glutamic acid, histamine, asparaginic acid, histidine, lysine, alanine and leucine etc. The largest amount among the amino acid composing VT2 was methionine.