• 제목/요약/키워드: microbial enzyme

검색결과 573건 처리시간 0.027초

Arthrobacter nicotianae에 의한 N-acetylglucosamine의 생산 (Microbial Production of N-Acetylglucosamine by Arthrobacter nicotianae)

  • 장지윤;김인철;장해춘
    • 한국식품과학회지
    • /
    • 제35권6호
    • /
    • pp.1188-1192
    • /
    • 2003
  • 새우나 게 껍질로부터 chitin을 유일한 탄소원으로 하는 집적배양에 의하여 chitinase 활성이 우수한 균주를 2종 분리하였다. 분리균주는 형태학적, 그람염색, 16s rDNA 서열분석을 통하여 Arthrobacter nicotianae로 동정되어, 각각 Arthrobacter nicotianae CH4와 Arthrobacter nicotianae CH13으로 명명하였다. 두 종의 분리균주로부터의 chitinase는 모두 pH $3.0{\sim}9.0$에서 90% 이상의 효소활성을 유지하여 높은 pH안정성을 나타내었다. 온도의 영향은 $20{\sim}60^{\circ}C$ 구간에서 최적 효소 활성의 $70{\sim}90%$를 유지하여 열안정성도 뛰어났다. A. nicotianae CH4와 A. nicotianae CH13이 분비하는 chitinase 조효소를 0.1% colloidal chitin 기질에 반응시켜서 반응산물로 생산되는 chitin 올리고당을 HPLC를 사용하여 분석하였다. A. nicotianae CH4 조효소에 의한 효소반응산물로는 올리고머인 $(GlcNAc)_4$이, A. nicotianae CH13는 단량체인 $(GlcNAc)_1$이 전체 반응산물의 각각 98% 이상 생성되었다.

Induction of Systemic Resistance against Cucumber mosaic virus in Arabidopsis thaliana by Trichoderma asperellum SKT-1

  • Elsharkawy, Mohsen Mohamed;Shimizu, Masafumi;Takahashi, Hideki;Ozaki, Kouichi;Hyakumachi, Mitsuro
    • The Plant Pathology Journal
    • /
    • 제29권2호
    • /
    • pp.193-200
    • /
    • 2013
  • Trichoderma asperellum SKT-1 is a microbial pesticide that is very effective against various diseases. Our study was undertaken to evaluate T. asperellum SKT-1 for induction of resistance against yellow strain of Cucumber mosaic virus (CMV-Y) in Arabidopsis plants. Disease severity was rated at 2 weeks post inoculation (WPI). CMV titre in Arabidopsis leaves was determined by indirect enzyme-linked immunosorbent assay (ELISA) at 2 WPI. Our results demonstrated that among all Arabidopsis plants treated with barley grain inoculum (BGI) of SKT-1 NahG and npr1 plants showed no significant reduction in disease severity and CMV titre as compared with control plants. In contrast, disease severity and CMV titre were significantly reduced in all Arabidopsis plants treated with culture filtrate (CF) of SKT-1 as compared with control plants. RT-PCR results showed increased expression levels of SA-inducible genes, but not JA/ET-inducible genes, in leaves of BGI treated plants. Moreover, expression levels of SA- and JA/ET-inducible genes were increased in leaves of CF treated plants. In conclusion, BGI treatment induced systemic resistance against CMV through SA signaling cascade in Arabidopsis plants. While, treatment with CF of SKT-1 mediated the expression of a majority of the various pathogen related genes, which led to the increased defense mechanism against CMV infection.

축사 내 황화수소와 암모니아의 저감방안 고찰: 한중비교 (Literature review of the Reduction of Hydrogen Sulfide and Ammonia in Livestock Pen: Comparison between Korean and Chinese cases)

  • 딩옌;문찬석
    • 한국산업보건학회지
    • /
    • 제29권4호
    • /
    • pp.442-451
    • /
    • 2019
  • Objectives: The aim of this study was to review the reduction methods for ammonia (NH3) and hydrogen sulfide (H2S) exposure in livestock. Methods: By reviewing domestic and international research reports from Korea and China, reducing ammonia and hydrogen sulfide in livestock pens was analyzed in terms of ventilation, deodorant, and feed additives. In addition, exposure limits in Korea and China were examined through a comparison between 'TLV-TWA and STEL under the Industrial Safety and Health Act in Korea' and 'Management Standards for Air of Livestock Pens in China'. Results and Discussion: In order to effectively control hazardous gases and odors in livestock pens, the enhancement of natural ventilation or the addition of ventilation fans at the pollution source are being examined. Deodorants are used as adsorbents or masking deodorants. Additives to feed were zeolite powder, FeSO4·7H2O, enzymes, and microbial preparations. Use of feed additives was low-cost and had significant effects compared to other methods. Zeolite was the most commonly used in feed additive in Chinese cases and proved to be low-cost and effective for reducing harmful gases. Enzyme preparations were shown to stimulate the growth of livestock, but were expensive. Conclusions: This study reviewed and examined domestic and international research papers in Korea and China for reducing ammonia and hydrogen sulfide concentrations in livestock pens. More diverse research and the development of feed additives are needed.

Citric acid와 phytic acid가 첨가된 된장의 색도와 품질특성 (Color and Quality Properties of Doenjang Added with Citric Acid and Phytic Acid)

  • 곽은정;박완수;임성일
    • 한국식품과학회지
    • /
    • 제35권3호
    • /
    • pp.455-460
    • /
    • 2003
  • 된장의 생산성 증대 및 부가가치를 높이기 위한 방안으로 된장의 갈변을 억제하기 위해 0.25%와 0.5% citric acid와 phytic acid를 첨가하여 된장을 제조하고 이들 유기산이 색도와 품질특성에 미치는 영향을 알아보았다. 이를 위해 $30^{\circ}C$에서 80일간 저장하면서 pH, 산도, 아미노태 질소, 효소활성, 색, 갈변억제율, 미생물수를 측정하였고 관능검사도 실시하였다. Citric acid와 phytic acid 첨가농도와 발효기간이 증가함에 따라 산도와 갈변억제율은 더욱 증가하였고, pH, 아미노태 질소 및 효소활성은 더욱 저하되었다. 총균, 효모 및 젖산균수는 pH 저하의 영향을 받지 않았다. 관능검사결과, panel들은 갈색 정도의 차이만을 유의적으로 인식하였고 향, 구수한 맛, 신맛, 기호도는 유의성이 인정되지 못하였다. 한편 0.25% 첨가시는 갈변은 억제되면서 품질특성뿐 아니라 관능적 특성도 대조구와 유사하였다. 이와 같은 사실로부터 citric acid와 phytic acid는 새로운 된장의 갈변억제제로 활용할 수 있을 것으로 사료되었다.

The effects of low-protein diets and protease supplementation on broiler chickens in a hot and humid tropical environment

  • Law, Fang Lin;Zulkifli, Idrus;Soleimani, Abdoreza Farjam;Liang, Juan Boo;Awad, Elmutaz Atta
    • Asian-Australasian Journal of Animal Sciences
    • /
    • 제31권8호
    • /
    • pp.1291-1300
    • /
    • 2018
  • Objective: This experiment was conducted to investigate the effects of dietary crude protein (CP) level and exogenous protease supplementation on growth performance, serum metabolites, carcass traits, small intestinal morphology and endogenous protease activity in broiler chickens reared under a tropical climate. Methods: A total of 480 day-old male broiler chicks were randomly assigned to eight dietary treatments in a $4{\times}2$ factorial arrangement. The main effects were CP level (21.0%, 19.7%, 18.5%, or 17.2% from 1 to 21 days and 19.0%, 17.9%, 16.7%, or 15.6% from 22 to 35 days) and protease enzyme supplementation (0 ppm or 500 ppm). All experimental diets were fortified with synthetic feed-grade lysine, methionine, threonine and tryptophan to provide the minimum amino acid recommended levels for Cobb 500. Results: Reducing dietary CP linearly reduced (p<0.05) growth performance, serum albumin, total protein, and carcass traits and increased (p<0.05) serum triglycerides and abdominal fat. There was no consistent effect of reducing dietary CP on morphological parameters of the intestine and on the pancreatic and intestinal endogenous protease activity (p>0.05). Protease supplementation improved (p<0.05) feed conversion ratio, body weight gain, carcass yield and intestinal absorptive surface area. Conclusion: Protease supplementation, as measured by growth performance, intestinal morphology and carcass yield, may alleviate the detrimental effects of low protein diets in broiler chickens.

Isolation and Characterization of Bacteriophages Against Pseudomonas syringae pv. actinidiae Causing Bacterial Canker Disease in Kiwifruit

  • Yu, Ji-Gang;Lim, Jeong-A;Song, Yu-Rim;Heu, Sunggi;Kim, Gyoung Hee;Koh, Young Jin;Oh, Chang-Sik
    • Journal of Microbiology and Biotechnology
    • /
    • 제26권2호
    • /
    • pp.385-393
    • /
    • 2016
  • Pseudomonas syringae pv. actinidiae causes bacterial canker disease in kiwifruit. Owing to the prohibition of agricultural antibiotic use in major kiwifruit-cultivating countries, alternative methods need to be developed to manage this disease. Bacteriophages are viruses that specifically infect target bacteria and have recently been reconsidered as potential biological control agents for bacterial pathogens owing to their specificity in terms of host range. In this study, we isolated bacteriophages against P. syringae pv. actinidiae from soils collected from kiwifruit orchards in Korea and selected seven bacteriophages for further characterization based on restriction enzyme digestion patterns of genomic DNA. Among the studied bacteriophages, two belong to the Myoviridae family and three belong to the Podoviridae family, based on morphology observed by transmission electron microscopy. The host range of the selected bacteriophages was confirmed using 18 strains of P. syringae pv. actinidiae, including the Psa2 and Psa3 groups, and some were also effective against other P. syringae pathovars. Lytic activity of the selected bacteriophages was sustained in vitro until 80 h, and their activity remained stable up to 50℃, at pH 11, and under UV-B light. These results indicate that the isolated bacteriophages are specific to P. syringae species and are resistant to various environmental factors, implying their potential use in control of bacterial canker disease in kiwifruits.

사료 및 보조사료로서의 생균제 급여에 따른 돈사 환경개선과 돼지 생산성에 미치는 영향 (Effects of the Feed and Probiotic Feeding on the Improvement of Hoggery Environment and the Productivity of Swine)

  • 이은영;임정수
    • 한국미생물·생명공학회지
    • /
    • 제39권3호
    • /
    • pp.200-209
    • /
    • 2011
  • 동물은 고기, 우유, 및 달걀과 같은 중요한 산물을 생산한다. 현대사회의 도시화과정 및 고도 성장은 보다 많은 동물성 산물을 요구하고 작은 농장에서 밀집화된 사육이 이루어지게 되는 원인이 되었다. 결과적으로 가축 분뇨생산량이 증가되었으며, 그에 따른 악취문제도 필연적인 결과로 나타났다. 분뇨로 인한 악취문제를 해결하지 못할 경우 축산업의 지속적인 발전과 환경개선을 이루는 큰 장애가 될 것이다. 축산환경으로 생산되는 악취는 휘발성지방산, 암모니아와 휘발성아민, 인돌과 페놀, 그리고 황화합물 네 종류로 분류된다. 질소성분의 절반이상은 뇨로 배설되기 때문에 동물을 사육하는 과정에서 저단백 사료와 합성아미노산을 급여시키고, 소화효소나 미생물제제 혹은 생균제를 사료에 첨가시켜줄 경우 질소원의 배출량을 감소시켜줄 수 있는 중요한 방법이 될 것이다. 따라서, 축산환경의 개선과 축산분야의 생산성을 향상시켜주기 위하여 사료 및 보조사료를 급여하는 다양한 시도가 진행되고 있다.

Effective Microwell Plate-Based Screening Method for Microbes Producing Cellulase and Xylanase and Its Application

  • Kim, Jennifer Jooyoun;Kwon, Young-Kyung;Kim, Ji Hyung;Heo, Soo-Jin;Lee, Youngdeuk;Lee, Su-Jin;Shim, Won-Bo;Jung, Won-Kyo;Hyun, Jung-Ho;Kwon, Kae Kyoung;Kang, Do-Hyung;Oh, Chulhong
    • Journal of Microbiology and Biotechnology
    • /
    • 제24권11호
    • /
    • pp.1559-1565
    • /
    • 2014
  • Cellulase and xylanase are main hydrolysis enzymes for the degradation of cellulosic and hemicellulosic biomass, respectively. In this study, our aim was to develop and test the efficacy of a rapid, high-throughput method to screen hydrolytic-enzyme-producing microbes. To accomplish this, we modified the 3,5-dinitrosalicylic acid (DNS) method for microwell plate-based screening. Targeted microbial samples were initially cultured on agar plates with both cellulose and xylan as substrates. Then, isolated colonies were subcultured in broth media containing yeast extract and either cellulose or xylan. The supernatants of the culture broth were tested with our modified DNS screening method in a 96-microwell plate, with a $200{\mu}l$ total reaction volume. In addition, the stability and reliability of glucose and xylose standards, which were used to determine the enzymatic activity, were studied at $100^{\circ}C$ for different time intervals in a dry oven. It was concluded that the minimum incubation time required for stable color development of the standard solution is 20 min. With this technique, we successfully screened 21 and 31 cellulase- and xylanase-producing strains, respectively, in a single experimental trial. Among the identified strains, 19 showed both cellulose and xylan hydrolyzing activities. These microbes can be applied to bioethanol production from cellulosic and hemicellulosic biomass.

Biochemical Characterization of a GDSL-Motif Esterase from Bacillus sp. K91 with a New Putative Catalytic Mechanism

  • Ding, Junmei;Yu, Tingting;Liang, Lianming;Xie, Zhenrong;Yang, Yunjuan;Zhou, Junpei;Xu, Bo;Li, Junjun;Huang, Zunxi
    • Journal of Microbiology and Biotechnology
    • /
    • 제24권11호
    • /
    • pp.1551-1558
    • /
    • 2014
  • The esterase gene Est8 from the thermophilic bacterium Bacillus sp. K91 was cloned and expressed in Escherichia coli. The monomeric enzyme exhibited a theoretical molecular mass of 24.5 kDa and an optimal activity around $50^{\circ}C$ at pH 9.0. A model of Est8 was constructed using a hypothetical YxiM precursor structure (2O14_A) from Bacillus subtilis as template. The structure showed an ${\alpha}/{\beta}$-hydrolase fold and indicated the presence of a typical catalytic triad consisting of Ser-11, Asp-182, and His-185, which were investigated by site-directed replacements coupled with kinetic characterization. Asp-182 and His-185 residues were more critical than the Ser-11 residue in the catalytic activity of Est8. A comparison of the amino acid sequence showed that Est8 could be grouped into the GDSL family and further classified as an SGNH hydrolase. Est8 is a new member of the SGNH hydrolase subfamily and may employ a different catalytic mechanism.

Purification and Characterization of Six Fibrinolytic Serine-Proteases from Earthworm Lumbricus rubellus

  • Cho, Il-Hwan;Choi, Eui-Sung;Lim, Hun-Gil;Lee, Hyung-Hoan
    • BMB Reports
    • /
    • 제37권2호
    • /
    • pp.199-205
    • /
    • 2004
  • The six lumbrokinase fractions (F1 to F6) with fibrinolytic activities were purified from earthworm Lumbricus rubellus lysates using the procedures of autolysis, ammonium sulfate fractionation, and column chromatography. The proteolytic activities on the casein substrate of the six iso-enzymes ranged from 11.3 to 167.5 unit/mg with the rank activity orders of F2 > F1 > F5 > F6 > F3 > F4. The fibrinolytic activities of the six fractions on the fibrin plates ranged from 20.8 to 207.2 unit/mg with rank orders of F6 > F2 > F5 > F3 > F1 > F4. The molecular weights of each iso-enzyme, as estimated by SDS-PAGE, were 24.6 (F1), 26.8 (F2), 28.2 (F3), 25.4 (F4), 33.1 (F5), and 33.0 kDa (F6), respectively. The plasminogen was activated into plasmin by the enzymes. The optimal temperature of the six iso-enzymes was $50^{\circ}C$, and the optimal pH ranged from pH 4-12. The four iso-enzymes (F1-F4) were completely inhibited by PMSF. The two enzymes (F5 and F6) were completely inhibited by aprotinin, TLCK, TPCK, SBTI, LBTI, and leupeptin. The N-terminal amino acid (aa) sequences of the first 20 to 22 residues of each fraction had high homology. All six isoenzymes had identical aa residues 2-3 and 13-15. The N-terminal 21-22 aa sequences of the F2, F3, and F4 isoenzymes were almost the same. The N-terminal aa sequences of F5 and F6 were identical.