• 제목/요약/키워드: ${\alpha}$-glucan

검색결과 123건 처리시간 0.024초

효모의 베타-1,3-글루칸 생합성 결함을 초래하는 돌연변이 유전자(soo1-1)의 분리 및 분석 (Isolation and Analysis of the Yeast Mutant Gene, soo1-1, which Confers the Defect in $\beta$-1,3-glucan Biosynthesis)

  • 이재준;이동원;김기현;박희문
    • 미생물학회지
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    • 제37권1호
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    • pp.42-48
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    • 2001
  • 출아 효모인 Saccharomyces cerevisiae의 베타-1,3-글루칸 생합성의 결함을 초래하는 돌연변이 유전자(sool-1)를 분리하여 돌연변이 부위의 염기서열을 결정하고 그 특성을 분석하였다. cool-1 유전자의 염기서열 분석 결과, 681번의 염기인 G가 A로 치환되어 Soolp의 $Gly^{227}$이 Asp로 치환되는 결과를 나타내는 것으로 판명되었고, cool-1 유전자는 기존에 보고된 retl-1 유전자와 동일한 돌연변이 유전자로 판명되었다. 그러나, ret1-1이 나타내는 온도감수성 형질은 배지에 1.2 M sorbitol 등의 삼투안정제를 첨가하면 극복될 수 있으며, cool-l/retl-1의 돌연변이 부위가 세포벽합성 관련 단백질의 번역 후 수식과정에 영향을 미친 것임을 확인하였다. 한편, Soolp/$\alpha$-COP의 N-말단에 존재하는 6개의 WD40 domain중 5번째 WD40 domain이 효모의 세포벽 합성이나 구조유지에 중요한 역할을 담당할 것임을 시사하는 결과를 얻었다.

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전분흡착에 의한 Cyclodextrin Glucanotransferase의 회수 (Recovery of Cyclodextrin Glucanotransferase by Adsorption to Starch)

  • 김진현;홍승서;이현수
    • KSBB Journal
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    • 제16권2호
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    • pp.128-132
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    • 2001
  • 발효 배양액으로부터 균체를 제거한 후에 전분파의 흡착성 을 증가시켜주기 위하여 ammonium sulface 25% (w/v), 반응 2시간 정도면 95% 이상의 효소가 전분(힐반전분 1%, wfv)에 홉착됨올 일 수 있었다. 효소 흡착인 경우 일반전분(옥수수 전분)이 흡착율 95% 이상으로 가장 효과적이며 탈착의 경우 (탈착용액 : 증류수)에는 산화천분이 1 회 68%로 가장 효과적이었다. 또한 효소의 홉착 및 탈착에 사용되는 전분익 농도 는 효소 역가 205 U/mL 기준으로 1 % (v/v) 정도면 효소의 흡착 및 탈착에 적당하였다. 효소 흡착외 경우 $4^{circ}C$, 정도에서, 탈착의 경우 온도 $50^{circ}C$, 와 pH 8.0에서 효과적이었다 탈착 용액으로 Iris-buffer가 탈착율 98%로 가장 효과적이었다. 또한 발효배양액으토부터 균체외 제거단계의 유무에 관계없이 전분의 흡착율과 탈착율은 유사하였다.

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신령버섯(Agaricus brasiliensis) 자실체 추출 조다당류의 항암 및 면역증강 작용 (Antitumor and Immuno-potentiating Activities of Crude Polysaccharides from Fruiting Body of Agaricus brasiliensis)

  • 차윤정;김정화;이태수;이우윤
    • 한국균학회지
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    • 제39권1호
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    • pp.57-67
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    • 2011
  • 신령버섯은 담자균문, 주름버섯목, 주름버섯과에 속하는 식용버섯으로 혈당, 혈압강하효과와 콜레스테롤 저하, 항종양, 암예방 효과가 있는 것으로 알려져 있다. 신령버섯의 자실체로부터 메탄올, 중성염용액 및 열수 등을 이용하여 조다당류를 추출하고 성분을 분석한 결과 ${\beta}$-glucan은 21.54~32.31%, 단백질은 0.16~9.34%로 구성되어 있는 것이 밝혀졌고 신령버섯 추출 조다당류를 Sarcoma 180, HT-29, NIH3T3 및 RAW 264.7 등의 암세포 및 정상세포에 대한 독성을 조사한 결과 10~2000 ${\mu}g/ml$의 조다당류 농도에서 각각의 세포는 세포독성을 나타내지 않았다. Sarcoma 180으로 접종된 ICR 생쥐에 신령버섯의 자실체에서 추출한 각각의 조다당류를 투여한 실험군은 대조군에 비해 수명이 각각 18.8~50.6% 연장되었다. 비장세포의 증식능과 B 임파구의 활성화에 미치는 alkaline phosphatase의 활성을 조사한 결과 비장 세포 증식능은 대조군에 대해 1.1~1.2배의 증식능을 보였고 B 임파구의 활성은 대조군에 대해 1.2~1.6배 증가하였다. 또한 버섯추출 조다당류를 투여한 실험군이 대조군에 비하여 대식세포에서 1.3~4.3배의 많은 nitric oxide를 발생시켰다. 비장세포에 여러 농도의 조다당류를 처리한 후 TNF-${\alpha}$, IL-$1{\beta}$, IL-2 및 IL-6 등의 사이토카인 분비량을 측정한 결과 생성된 사이토카인의 양은 대조군에 비해 2.2배 높게 나타났다. 중성염용액추출 조다당류를 50 mg/kg body weight의 농도로 투여한 실험군 생쥐의 총 복강 세포 수는 대조군에 비하여 4배 증가하였고, 열수추출 조다당류를 50 mg/kg body weight의 농도로 투여한 실험군 생쥐의 백혈구 수는 대조군에 비하여 각각 2.7배 증가하였다. 혈액생화학적 검사를 시행한 결과, 대조군과 유사한 경향을 나타냈다. 따라서 신령버섯의 자실체에서 추출한 조다당류는 생쥐의 면역을 증강시키는 것은 물론 Sarcoma 180에 대한 항암효과를 나타내는 것으로 밝혀졌다.

Purification and Characteristics of Glucoamylase in Aspergillus oryzae NR 3-6 Isolated from Traditional Korean Nuruk

  • Yu, Tae-Shick;Kim, Tae-Hyoung;Joo, Chong-Yoon
    • Journal of Microbiology
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    • 제37권2호
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    • pp.80-85
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    • 1999
  • The purification system of glucoamylase (glucan 1,4-${\alpha}$-glucosidase, EC 3. 2. 1. 3), some characteristics of the purified enzyme and hydrolysis rate of various raw starch were investigated through several experiments. The enzyme was produced on a solid, uncooked wheat bran medium of Aspergillus oryzae NR 3-6 isolated from traditional Korean Nuruk. The enzyme was homogeneously purified 6.8-fold with an overall yield of 28.3% by the criteria of disc- and SDS-polyacrylamide gel electrophoresis. The molecular weight was estimated to be 48 kDa by SDS-PAGE. The optimum temperature and pH were 55$^{\circ}C$ and 4.0, respectively. The enzyme was stable at a pH range of 3.0∼10.0 and below 45$^{\circ}C$. Enzyme activity was inhibited about 27% by 1mM Hg2+. The hydrolysis rate of raw wheat starch was shown to be 17.5-fold faster than the hydrolysis rate of soluble starch. The purified enzyme was identified as glucoamylase because the product of soluble starch by the purified enzyme was mainly glucose by thin layer chromatography.

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Streptomyces의 mutanase 유도에 관한 연구 (A STUDY ABOUT THE INDUCTION OF MUTANASE FROM STREPTOMYCES)

  • 양규호;정진
    • 대한소아치과학회지
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    • 제23권3호
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    • pp.764-773
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    • 1996
  • The mutan containing $\alpha$-1,3 bond is an insoluble portion of glucan which is the main component of dental plaque. The secretion of mutanase was assessed with mutan-digesting Streptomyces isolated from soil, and the factors affecting its activity was studied, obtaining the following result. Mutan-digesting Streptomyces was identified as Streptomyces exfoliatus by its characteristics. The effect of dextranase was identified on the media containing blue dextran. A clear zone was produced by Streptomyces exfoliatus on the media containing blue mutan, so showing the secretion of mutanase. A clear zone was significantly produced on the media overlayed with agar containing blue mutan. A clear zone was produced at 2 days after the inoculation of Streptomyces exfoliatus on the media containing below a concentration of 0.025% glucose, at 3 days on the media containing 0.05 % glucose, and at 4 days on the media containing 0.1 % glucose. Mutan-digestion wasn't appeared early by adding other carbohydrates. The higher concentration of peptone, the later appearance of clear zone was on the media containing below a concentration of 0.1 % peptone. These results indicated that the secretion of mutanase was identified from mutan-digesting Streptomyces on the media containing blue mutan, and a clear zone was appeared lately on the media containing higher amount of glucose.

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Capsaicin이 연수후각의 흥분성 아미노산 전달물질에 미치는 영향 (Effect of Capsaicin on the Excitatory Amino Acids Neurotranmitters in Medullary Dorsal Horn)

  • 권수경;윤수한;이종흔
    • Restorative Dentistry and Endodontics
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    • 제19권2호
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    • pp.621-632
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    • 1994
  • This experiment was performed to study the effect of capsaicin on the excitatory amino acids (EAAs) neurotransmitter in medullary dorsal horn and to clarify the relationship between substance P and excitatory amino acids. Horizontal slice of rat medullary dorsal horn was prepared and perfused with modified Krebs-Ringer solution in brain slice chamber. Release of EAAs was induced by veratrine and capsaicin were added to perfusion solution to observe the changes in EAA release. Capsaicin and ruthenium red, capsaicin antagonist, were also systemically injected with 50mg/kg in first day and 100mg/kg in second day for 2 days. Medulla oblongata containing the medullary dorsal horn was isolated, homogenized and centrifused. Spernatant was freeze-dried and EAA was determined by HPLC. Release of glutamate and aspartate was significantly increased by veratrine or capsaicin, but veratrine evoked release of EAAs was blocked by capsaicin in vitro, and injected ruthenium red did not have effect on the contents of EMs in vivo. Systemically injected capsaicin evoked the slight decrease in content of glutamate and aspartate in medullary dorsal horn and this effect of capsaicin was unaffected by ruthenium red.

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대두 $\beta$-amylase Isozyme의 분리 및 정제 (Separation and Purification of Soybean $\beta$-amylase Isozymes)

  • 지의상
    • 한국식품영양학회지
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    • 제3권2호
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    • pp.149-160
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    • 1990
  • The soybean $\beta$-amylase ($\alpha$-1, 4-glucan maltohydrolase, EC 3.2.1.2) is composed of seven isozymes(I', I, II, III, IV, V and VI), and isozyme II and IV are the main components among these. The Purification of $\beta$-amylase isozymes from soybean whey were performed by ammonium sulfate fractionation, CM-Sephadex C-50 column chromatography, DEAE-Sephadex chromatography and Gel filtration. The resulted purity of $\beta$-amylase was throughly confirmed by electrophoresis, and then determined its isoelectric point and molecular weight. The results obtained were as follows, 1. Five active fractions of soybean p-amylase were derived on CM-Sephadex C-50 column chromatography. 2. Seven active bands of p-amylase isozymes were detected by isoelectric focusing gel electrophoresis, and their isoelectric points(I' to VI) were 5.07, 5.15, 5.25, 5.40, 5.55, 5.70 and 5.93, respectively. 3. Isozyme II and IV were main components of soybean $\beta$-amylase. 4. The molecular weights of both isozyme II and IV were determined to be 56,000 daltons by the result of SDS polyacrylamide gel electrophoresis. 5. Km values of main isozyme II & IV for amylopectin were determined to be 2.25 mg/ml, which suggest the same function of each isozyme.

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한국산 동백나무겨우살이에서 추출한 수용성 리그닌-탄수화물 복합체의 구조분석 (Structural Analysis of Water Soluble Lignin-Carbohydrate Complex(LCC) Isolated from Korean Camellia Mistletoe(Pseudixus japonicus Hayata))

  • 최준원;안원영
    • Journal of the Korean Wood Science and Technology
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    • 제25권3호
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    • pp.1-7
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    • 1997
  • 한국산 동백나무겨우살이(Pseudixus japonicus Hayata)에 존재하는 수용성 리그닌-탄수화물 복합체를 구성하는 다당류의 구조를 밝히고 리그닌 성분과 다당류의 결합양식을 구명하고자, 냉 온수 추출한 수용성 리그닌-탄수화물 복합체(M-LCC-WE)를 DEAE Sephadex A-50로 중성분획(M-LCC-N)과 산성분획(M-LCC-A), 나머지분획(M-LCC-R)으로 세분화한 후 M-LCC-N과 M-LCC-A에 대하여 메틸화, 아세틸화, 그리고 DDQ 산화반응을 실시하였다. M-LCC-N을 구성하는 다당류는 ($1{\rightarrow}4$) 글리코시드결합의 arabinan과 ($1{\rightarrow}4$)나 ($1{\rightarrow}6$) 글리코시드결합의 galactan과 glucan으로 M-LCC-A의 다당류는 ($1{\rightarrow}4$) 글리코시드결합의 arabinan과 ($1{\rightarrow}6$) 글리코시드결합의 galactan이 다당류 주성분으로 밝혀졌으며 galacturonic acid가 결합되어 있기 때문에 산성적 성질을 나타내고 있었다. 또한 M-LCC-A에서는 galacturonic acid 의 carboxyl 그룹이 리그닌의 ${\alpha}$-와 ${\gamma}$-위치에서 ester결합이 존재함이 확인되었다.

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느타리속 버섯류의 영양성분 및 생리활성 (Physiological Activity and Nutritional Composition of Pleurotus Species)

  • 엄수나;진경언;박계원;유영복;박기문
    • 한국식품과학회지
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    • 제42권1호
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    • pp.90-96
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    • 2010
  • 일반 느타리 13품종과 색상 느타리 5품종을 사용하여 아미노산 및 polyphenol, $\beta$-glucan 함량을 분석하고, 생리활성으로 항산화 및 항암, 항고혈압, 항혈전, 항당뇨, 항염활성을 측정하였다. 느타리버섯 18종의 아미노산 분석결과 전반적으로 감칠맛을 내는 glutamic acid 함량이 비교적 많이 함유되어 있었고, 필수아미노산 성분도 고르게 분포되어 있었다. Polyphenol 함량에서는 전품종에서 20 mg% 함량이상을 나타냈으며, 노랑느타리(R)가 $39.13{\pm}0.82\;mg%$로 가장 높았다. $\beta$-glucan 함량은 노랑느타리(R)에서 $37.67{\pm}0.22%$로 가장 높았으며, 그 외에 원형1(C), 장안PK(A)에서 각각 $28.75{\pm}0.61%$, $27.95{\pm}0.33%$의 순으로 나타났다. 전자공여능에서는 노랑느타리(R) 버섯의 DPPH $IC_{50}$값이 $2.93{\pm}0.44\;mg/mL$로 가장 낮아 항산화 활성이 가장 우수한 것으로 나타났으며, 세포독성 실험에서는 노랑느타리(R) 에탄올 추출물 1% 처리시 신장 암세포에 대해 36.90%의 세포 억제율을 보였다. ACE 저해활성의 경우 노랑느타리(R) 에탄올 추출물 1%농도에서 $60.5{\pm}0.2%$의 저해율이 측정되었고, 흑평(B) $56.7{\pm}1.1%$, 여름(H) $52.4{\pm}1.3%$ 수준으로 나타났다. 항혈전 활성에서는 3%농도에서 흑평(B)과 삼복(G)을 제외한 나머지 느타리버섯 에탄올 추출물에서 50%이상의 용해 활성을 보였으며 노랑느타리(R)에서 거의 plasmin과 동등한 활성을 나타냈다. 항당뇨 활성에서는 노랑느타리(R)의 경우 $50.5{\pm}0.8%$의 비교적 높은 효소저해율이 측정되었고, 항염활성에서는 노랑느타리(R)에서 $68.4{\pm}0.3%$의 억제율이 측정되었다. 이상의 결과로 일반 느타리 13 품종과 육종 재배된 색상 느타리 5품종 중 노랑느타리(R)가 가장 우수한 생리활성을 나타내 향후 기능성 소재로의 활용가능성이 기대되었다.

정상 및 병적체액중 동종효소분획에 관한 연구 (Study on the Pattern of Isoenzymes in Pancreatic Juice, Serum and Saliva of Rabbit)

  • 김원준;김혜영;이향우;홍사석
    • 대한약리학회지
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    • 제16권2호
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    • pp.15-24
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    • 1980
  • [${\alpha}$]-Amylase catalyses the hydrolysis of starch, glycogen, and related poly- and oligosac-charide by random cleavage of ${\alpha}$-D-(l-4) glucan linkage. In man large amounts of amylase are secreted into the digestive tract by the salivary and exocrine pancreatic gland, minimal amount being produced also in other tissues. It has been known that ${\alpha}$-amylase exists in multiple molecular forms, isoenzyme which can be separated from each other because of difference in their physicochemical properties. By using various methods, several groups of investigator have separated the many isoenzyme in serum, saliva and pancreatic juice. Furthermore, changes of the normal serum isoenzyme pattern is diagnostically useful even when the total serum enzyme activity is noninformative, such as the clinical use of isoenzyme of serum lactate dehydrogenase. Procarboxypeptidase-A which is one of the pancreatic enzymes is also present as isoenzymes. Four forms of procarboxypeptidase-A haye been found in the bovine enzyme and three forms of the porcine enzyme. In human pancreatic juice four forms of procarboxypeptidase-A isoenzyme were found by isoelectric focusing method. Recently, the so-called isoamylase analysis was developed for the diagnostic use of amylase in pancreatic diseases. In alcohotic patients, the serum concentration of pancreatic isoamylase is subnormal and this lowered activity provides strong evidence for pancreatic exocrine insufficiency. The purpose of this study was to elucidate the variations of the isoenzyme of amylase and procarboxypeptidase-A in serum, saliva and pancreatic juice of the experimental animals. The results are as follow. 1) Three main forms of isoenzyme of amylase by isoelectric focusing were found in pancreatic juice of normal rabbit. However, many new bands were appeared in the pancreatic juice of cholic acid administered animal intravenously while the infusion of cholic acid or elastase into pancreatic duct produced the decrease of number of the fractions on the isoelectric focusing. In the case of serum isoenzyme from normal animal, two major and a few minor isoamylases were observed. By injecting alcohol intravenousely the fractions of serum isoamylase were significantly decreased and in contrary to the pattern in the pancreatic juice the infusion of cholic acid or elastase into pancreatic duct exhitited a significant decrease of the isoenzyme of amylase fractions. In saliva from normal animal three main isoamylase were produced of the administration of alcohol. 2) In the case of procarboxypeptidase-A isoenzyme, two major fractions which have isoelectric point at 6.2 and 6.4 and other two minor bands were observed in the pancreatic juice of normal rabbit. By the treatment of the juice with trypsin, only one band was produced on the isoelectric focusing. No procarboxypeptidase was appeared on the electrofocusing by the infusion of cholic acid or phospholipase A into the pancreatic duct of rabbit. However, a single major fraction of procarboxypeptidase-A was appeared at 3 hr after simple ligation of the pancreatic duct. No significant changes were observed in the juice of the alcohol or cholic acid administered group.

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