전분으로부터 α-amylase에 의한 배당체의 합성

박종이,이태호,Park, Jong Yi,Lee, Tae Ho 한국미생물학회 1998 미생물학회지 Vol.34 No.3

수계에서 전분 가수분해 효소의 transglycosylation 반응을 이용하여 배당체(glycoside)를 합성하였다. Glycosyl donor인 가용성전분과 glycosyl acceptor인 benzylalcohol을 기질로 하여 ${\alpha}$-amylase에 의해 합성되는 배당체는 glucose의 1번 OH기에 benzylalcohol이 ${\alpha}$형태로 결합한 benzylalcohol-${\alpha}$-glucoside(BG)와 benzylalcohol-${\alpha}$-maltoside(BM)이었다. pH 5.0의 반응에서는 주로 BG가, pH 8.0의 반응에서는 BM만이 합성되는 특이한 반응양상을 보였다. Transglycosylation 반응의 최적조건은 가용성전분 50 mg/ml, benzylalcohol 50 mg/ml, 온도 $30-35^{\circ}C$, 효소량 10 unit/ml이었으며, 합성된 BG는 ${\alpha}$-glucodisase에 의해 glucose와 benzylalcohol로 가수분해되었으며 BM의 경우는 pH 5.0에서는 glucose와 BG로 가수분해되었으나 pH 8.0이상에서는 전혀 분해되지 않았다. BM과 구조적으로 유사한 maltotriose는 pH 5.0에서 glucose와 maltose로 가수분해 되었으나 transglycosylation반응은 거의 일어나지 않았으며 pH 8.0에서는 가수분해도 transglycosylation반응도 일어나지 않았다. Glycosides were synthesized using transglycosylation reaction of amylase in water system. The glycosides synthesized in water phase by a-amylase with starch as a glycosyl donor and benzylalcohol as an acceptor were identified as benzylalcohol-${\alpha}$-glucoside (BG) and benzylalcohol-${\alpha}$-maltoside (BM) of which one molecule of benzylalcohol was bound to 1-OH of glucose. The final products were BG in reaction system of pH 5.0, and BM in that of pH 8.0. The transglycosylation reaction by ${\alpha}$-amylase were carried out in water system containing 50 mg starch, 50 mg benzylalcohol, and 10 units enzyme at $30-35^{\circ}C$ for 3 days. The synthesized BG was hydrolyzed to glucose and benzylalcohol by ${\alpha}$-glucosidase, while ${\alpha}$-amylase hydrolyzed BM to glucose and benzylalcohol-${\alpha}$-glucoside in pH 5.0. Maltotriose resemble structurally to BM was rapidly hydrolyzed to glucose and maltose by ${\alpha}$-amylase at pH 5.0, being slightly hydrolyzed at pH 8.0, but not transglycosylated in present of benzylalcohol.

전분을 기질로 한 이상계에서 Amylase의 당전이반응에 의한 배당체의 합성

박종이,이재동,이태호,장경립 한국미생물학회 1999 미생물학회지 Vol.35 No.1

$\alpha$-Amylase 의 당전이반응에 의해 가용성전분으로부터 benzylalcohol-$\alpha$-glucoside(BG)를 합성하였다. 이 때 glycosyl 기의 공여체인 가용성전분 1%, glycosyl 기의 수용체인 benzylalcohol 90%, pH 5.0의 0.1M citrate 완충액 10%, Aspergillus oryzae 유래의 $\alpha$-amylase 10 unit를 함유하는 이상계(water-organic two phase )에서 당전이반응이 가장 효율적으로 일어났으며, $40^{\circ}C$, 80시간 정도의 반응에서 전문 10mg 으로부터 약 4mg 의 BG가 합성되었다. 합성초기에는 benzylalcohol-$\alpha$-maltoside(BM) 가 주로 생산되었다가 반응시간이 경과함에 따라 이는 가수분해되고 최종적으로는 BG 만이 생성되었다. 합성물질은 모두 환원력이 없고 $\alpha$-glucosidase 에 의해 가수분해되었드며 ESI-Mass 에 의해 분자량이 각각 270, 432로 측정되어 그 구조가 BG, BM 임을 확인하였다. Benzylalcohol-$\alpha$-glucoside (BG) was synthesized from soluble starch by transglycosylation of $\alpha$-amylase. Transglycosylation in water-organic two phase system containing 1% soluble starch as a glycosyl donor, 90% benzylalcohol as a glycosyl acceplor, 10% citrate buffer solulion (0.1 M, pH 5.0), and 10 unit of $\alpha$-amylase (Aspergilllw oryzae) was showed highcst efficiency. About 4 mg BG was obtained from 10 mg starch in reaction for 80 hrs at $40^{\circ}C$. Initially benzylalcohol-$\alpha$-maltoside Q3M) was major product, but as the reaction proceeded, it was hydrolyzed to glucose and BG. Finally the product of transglycosylation by $\alpha$-amylase was only BG. The both products did not show reducing powcr and hydrolyzed by $\alpha$-glucosidase and $\alpha$-amylase, respectively. The molecular wcights of both were estimated to be 270 and 432 by ES1-Mass, respectively.

전분으로부터 Amyloglucosidase의 당전이반응에 의한 배당체의 합성

박종이,이희정,이태호 한국산업미생물학회 1998 한국미생물·생명공학회지 Vol.26 No.2

수계에서 전분 가수분해효소의 transglycosylation반응을 이용하여 배당체(glycoside)를 합성하였다. Glycosyl donor인 starch와 glycosyl acceptor인 benzylalcohol을 반응기질로 선택하였다. 시판되는 9종의 당가수분해효소의 transglycosylation활성을 조사한 결과 glucose와 한 종류의 glycoside만을 생산하는 amyloglucosidase(from Rhizopus sp.)를 반응효소로 선정하였다. Amyloglucosidase에 의해 합성된 배당체는 여러 가지 분석을 통해 glucose의 1번 OH기에 benzylalcohol이 α형태로 결합된 benzylalcohol-α-glucoside(BG)임을 확인하였다. 수계에서 이 효소에 의한 transglycosylation 반응의 최적조건은 starch 50 ㎎/㎖, benzylalcohol 50 ㎎/㎖, 온도 45℃, 효소량 10 unit/㎖, pH 5.0, 반응시간 32시간이었으며 합성된 BG는 amyloglucosidase에 의해서는 분해되지 않았고 α-glucosidase에 의해 glucose와 benzylalcohol로 가수분해되었다. Glycosides were synthesized using transglycosylation reaction of amylase in water system. Starch as a glycosyl donor and benzylalcohol as an acceptor were selected as substrates of transglycosylation reaction. Among tested 9 commercial amylase, amyloglucosidase from Rhizopus sp. had high activity for transglycosylation from starch. The glycoside synthesized in water phase by amyloglucosidase was identified as benzylalcohol-α-glucoside (BG) of which one molecule of benzylalcohol was bound to 1-OH of gluose. The transglycosylation reaction by amyloglucosidase were carried out in reaction system containing 50 ㎎ starch, 50 ㎎ benzylalcohol, and 10 units enzyme in pH 5.0 at 45℃. The synthesized BG was hydrolyzed by α-glucosidase to produce glucose and benzylalcohol.

Expression and Functional Characterization of Recombinant Human Erythropoietin (rhEPO) Produced in the Milk of Transgenic Mice

권득남,박종이,이소영,황규찬,양민정,김진회 한국동물번식학회 2003 Reproductive & Developmental Biology(Supplement) Vol.27 No.1s

Expression and Functional Characterization of Recombinant Human Erythropoietin (rhEPO) Produced in the Milk of Transgenic Mice

권득남,박종이,이소영,황규찬,양민정,김진회 한국동물생명공학회(구 한국동물번식학회) 2003 Reproductive & developmental biology Vol.27 No.1

다양한 부위별 연 추출물의 항혈전 활성

안선미,성화정,김종식,박종이,손호용 한국미생물·생명공학회 2018 한국미생물·생명공학회지 Vol.46 No.4

To investigate the bio-activities of lotus (Nelumbo nucifera Gaertner), ethanol extracts were prepared from different parts of lotus, including lotus root, node of root (NR), leaf, pod of seed (PS), seed (S), and embryo of seed (ES), respectively. Anti-thrombosis activities were evaluated. NR, S, and PS extracts displayed strong anti-coagulation activities, as evidenced by the inhibition of thrombin, prothrombin, and coagulation factors, respectively. NR, leaf, S, and PS extracts displayed strong platelet aggregation inhibitory activities. The aggregation inhibition of S and PS extract was comparable to that of aspirin. The extracts of NR, S, and PS did not show hemolysis activity up to 1.0 mg/ml. 연(Nelumbo nucifera Gaertner)으로부터 신규의 유용 생리활성을 확인하기 위해, 연잎, 연자방, 연자육, 연자심, 우절 및 연근으로부터 각각 ethanol 추출물을 제조하고, 현재까지 보고되지 않은 항혈전 활성을 평가하였다. 그 결과, 연근, 연잎 및 연자심 추출물은 항응고 활성이 인정되지 않았으나, 우절, 연자방 및 연자육 추출물에서는 강력한 TT, PT, aPTT 연장효과를 나타내었으며, aspirin 보다 강력한 항응고 활성을 나타내었다. 또한 혈소판 응집저해 활성 평가 결과, 우절, 연잎, 연자방, 연자육 추출물에서 응집저해가 나타났으며, 가장 강력한 응집저해는 연자방과 연자육에서 확인된 바, 이는 아스피린에 필적하는 강력한 활성이었다. 상기활성 추출물은 1.0 mg/ml 농도까지 인간 적혈구 용혈활성이없음을 확인하여, 우절, 연자방 및 연자육 추출물이 신규의항혈전제로 사용 가능함을 제시하였다.

Synthesis and characterization of hydrothermally grown potassium titanate nanowires

Derya Kapusuz,Y. Eren Kalay,박종이,Abdullah Ozturk 한양대학교 세라믹연구소 2015 Journal of Ceramic Processing Research Vol.16 No.3

Potassium titanate (KT) nanowires were synthesized by a one-step hydrothermal reaction between TiO2 and aqueous KOH solution. The effects of KOH concentration and reaction time on hydrothermal formation and KT nanowire growth were investigated. The nanowire growth mechanism was elucidated using a combined study of powder X-ray diffraction, and scanning and transmission electron microscopy. The results revealed that hydrothermal growth was initiated by the formation of amorphous-like Ti-O-K sheets in anatase. Increasing hydrothermal reaction time caused the transformation of anatase to Ti-O-K sheets, from which potassium hexa-titanate (K2Ti6O13) nuclei formed and grew to establish one-dimensional morphology through preferential growth along the b-axis. It was revealed that the hydrothermal reactions followed a quite different mechanism than the well-known calcination route. Potassium tetra-titanate (K2Ti4O9) crystals formed in the amorphous region using the hexa-titanate phase as a nucleation site for heterogeneous crystallization. Increasing the KOH concentration in the solution accelerated the hydrothermal reaction rate.

MoS2-Nanosheet/Graphene-Oxide Composite Hole Injection Layer in Organic Light-Emitting Diodes

박민준,NGUYEN PHAN THANG,최경순,박종이,Abdullah Ozturk,김수영 대한금속·재료학회 2017 ELECTRONIC MATERIALS LETTERS Vol.13 No.4

In this work, composite layers comprising two-dimensionalMoS2 and graphene oxide (GO) were employed as holeinjection layers (HILs) in organic light-emitting diodes(OLEDs). MoS2 was fabricated by the butyllithium (BuLi)intercalation method, while GO was synthesized by amodified Hummers method. The X-ray diffraction patternsshowed that the intensity of the MoS2 (002) peak at 14.15°decreased with increase in GO content; the GO (001) peakwas observed at 10.07°. In the C 1s synchrotron radiationphotoemission spectra, the contributions of the C-O, C=O, and O-C=O components increased with increase in GO content. These results indicated that GO was well mixed with MoS2. The lateral size of MoS2 spanned from a few hundreds ofnanometers to 1 μm, while the size of GO was between 400 nm and a few micrometers. Thus, the coverage of the MoS2-GOcomposite on the ITO surface improved as the GO content increased, owing to the large particle size of GO. Notably, GO withlarge size could fully cover the indium tin oxide film surface, thus, lowering the roughness. The highest maximum powerefficiency (PEmax) was exhibited by the OLED with MoS2-GO 6:4 composite HIL, indicating that similar contents of MoS2 andGO in MoS2-GO composites provide the best results. The OLED with GO HIL showed very high PEmax (4.94 lm W−1) becauseof very high surface coverage and high work function of GO. These results indicate that the MoS2-GO composites can be usedto fabricate HILs in OLEDs.

표고버섯 수확 후 배지의 유용 생리활성 평가

성화정(Hwa-Jung Sung),표수진(Su-Jin Pyo),박종이(Jong-Yi-Park),손호용(Ho-Yong Sohn) 한국생명과학회 2019 생명과학회지 Vol.29 No.2

국내 표고버섯은 참나무 톱밥을 주 원료로 한 인공배지를 이용하여 재배하고 있으며, 표고버섯 재배 후 부산물로 발생하는 [수확 후 배지](Spent Mushroom Substrate: SMS)는 약 50,000톤으로 추정된다. 본 연구에서는 별도의 용도 없이 폐기되고 있는 표고버섯 SMS를 유용 생물자원으로 이용하기 위해, 1회 수확 후 SMS 및 3회 수확 후 SMS의 열수 추출물을 조제하여 이들의 항산화, 항균, 항당뇨, 항응고 및 혈소판 응집저해활성을 평가하였다. 대조구로는 재배용 살균배지 및 표고버섯의 열수 추출물을 이용하였다. 그 결과, 표고버섯 SMS 추출물은 표고버섯 및 살균배지 추출물보다 우수한 DPPH 음이온, ABTS 양이온 nitrite 소거능 및 환원력을 나타내었다. 1회 및 3회 SMS 추출물들은 0.5 mg/disc 농도에서는 사용된 세균 및 진균에 대한 항균력이 나타나지 않았으나, 0.5 mg/ml 농도에서 우수한 α-glucosidase 저해활성을 나타내었다. 또한 thrombin time, prothrombin time, activated partial thromboplastin time 및 혈소판 응집저해 활성 측정 결과, SMS 추출물들은 혈소판 응집에는 미미한 영향을 나타내었으나, 강력한 혈액응고저해 활성을 나타내어 항혈전 조성물로 개발 가능함을 확인하였다. 본 연구결과는 SMS를 폐기 대상이 아닌, 표고버섯 균사체가 대량 배양된 생물자원으로 고려하는 것이 필요함을 제시하며, SMS를 이용한 항산화, 항당뇨, 항혈전 조성물 개발이 가능함을 제시하고 있다. In Korea, shiitake mushroom, Lentinula edodes, is cultivated on artificial medium containing oak sawdust and wheat bran. The annual production of spent mushroom substrate (SMS) of shiitake, a byproduct of the mushroom industry, is estimated to reach over 50,000 tons per year. This study aimed to improve the use of SMS as a novel bioresource. Hot water extracts of SMS after the first and third harvest were prepared and their bioactivities evaluated. Hot water extracts of uninoculated medium and shiitake were used as controls. Extracts of SMS showed higher radical scavenging of DPPH anions, ABTS cations, nitrites, and a higher reducing power than those of shiitake or medium extracts. After the first and third harvests at 0.5 mg/disc, SMS extracts showed no antibacterial or antifungal activities against the pathogenic and food-spoilage bacteria and fungi. However, they showed good inhibitory activities against α-glucosidase at 0.5 mg/ml. In addition, SMS extracts had strong anti-coagulation activities via their inhibition of thrombin, prothrombin, and blood coagulation factors without platelet aggregation activity. Our results suggested SMS should no longer be perceived as a useless byproduct but should be understood as a novel bioresource, the extracts of which could be developed as antioxidant, antidiabetic, and antithrombosis agents.

Anti-Wrinkle Effect, Whitening Effect and Safety Test of Nelumbo nucifera Gaertner

Bo Seul Yeom(염보슬),Young Ah Jang(장영아),Jong Yi Park(박종이),Jin Tae Lee(이진태) 한국약용작물학회 2019 한국약용작물학회 학술대회논문집 Vol.2019 No.1