• 제목/요약/키워드: industrial mutant

검색결과 79건 처리시간 0.034초

자외선 조사에 의해 유도된 미세조류 Arthrospira platensis 변이주의 특성 (Characterization of Arthrospira platensis Mutants Generated by UV-B Irradiation)

  • 박현진;김영화;이재화
    • 공업화학
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    • 제23권5호
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    • pp.496-500
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    • 2012
  • Arthrospira platensis (A. platensis)는 상업적으로 중요한 사상형 미세조류이다. 화학적 혹은 물리적 돌연변이원에 의해 유도된 변이주 분리는 균주 개량에 중요하게 작용한다. 본 연구에서, A. platensis에서 자외선(UV-B)조사에 따른 영향을 살펴보았고, 그에 따른 변이주를 확보하였다. A. platensis를 자외선(15 Watt, 254 nm)을 이용하여 1, 3, 5, 10 min 동안 처리 한 후, 얻어진 변이주를 각각 UM1, UM3, UM5, UM10으로 명명하였다. 특히, UM5 변이주는 야생균주와 비교하여 지질의 함량이 8~11배 가량 크게 증가하였다. 또한, 카로티노이드 함량과 항산화 효소(peroxidase, superoxide dismutase) 활성이 증가하였다. 이 결과, 자외선에 의해 유도된 변이주는 생리활성 물질을 축적하였으며, 이러한 유용성분을 생산하는 미세조류의 균주 개발은 미세조류의 산업화를 촉진시킬 것으로 기대된다.

Analysis of Active Center in Hyperthermophilic Cellulase from Pyrococcus horikoshii

  • Kang, Hee-Jin;Ishikawa, Kazuhiko
    • Journal of Microbiology and Biotechnology
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    • 제17권8호
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    • pp.1249-1253
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    • 2007
  • A hyperthermostable endoglucanase from Pyrococcus horikoshii with the capability of hydrolyzing crystalline cellulose was analyzed. A protein engineering study was carried out to obtain a reduced-size mutant. Five amino acid residues at both the N- and C-terminus were found to be removable without any loss of activity or thermal stability. Site-directed mutagenesis was also performed on R102, N200, E201, H297, Y299, E342, and W377, residues possibly involved in the active center or in the recognition and binding of a cellulose substrate. The activity of the resulting mutants was considerably decreased, confirming that the mutated residues were all important for activity. A reduced-size enzyme, as active as the wild-type endoglucanase, was successfully obtained, plus the residues critical for its activity and specificity were confirmed. Consequently, an engineered enzyme with a reduced size was obtained, and the amino acids essential for activity were confirmed by site-directed mutagenesis and comparison with a known three-dimensional structure.

Malonate Metabolism: Biochemistry, Molecular Biology, Physiology, and Industrial Application

  • Kim, Yu-Sam
    • BMB Reports
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    • 제35권5호
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    • pp.443-451
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    • 2002
  • Malonate is a three-carbon dicarboxylic acid. It is well known as a competitive inhibitor of succinate dehydrogenase. It occurs naturally in biological systems, such as legumes and developing rat brains, which indicates that it may play an important role in symbiotic nitrogen metabolism and brain development. Recently, enzymes that are related to malonate metabolism were discovered and characterized. The genes that encode the enzymes were isolated, and the regulation of their expression was also studied. The mutant bacteria, in which the malonate-metabolizing gene was deleted, lost its primary function, symbiosis, between Rhizobium leguminosarium bv trifolii and clover. This suggests that malonate metabolism is essential in symbiotic nitrogen metabolism, at least in clover nodules. In addition to these, the genes matB and matC have been successfully used for generation of the industrial strain of Streptomyces for the production of antibiotics.

제 1차 한.중 생명공학 심포지움 (Practice of industrial strain improvement)

  • Lei, Zhao-zu
    • 미생물과산업
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    • 제19권2호
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    • pp.34-41
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    • 1993
  • Industrial strain improvement is concerned with developing or modifying microorganisms used in production of commercially important fermentation products. The aim is to reduce the production cost by improving productivity of a strain and manipulating specific characteristics such as the ability to utilize cheaper raw materials or resist bacteriophages. The traditional empirical approach to strain improvement is mutation combined with selection and breeding techniques. It is still used by us to improve the productivity of organisms in amino acids, organic acids and enzymes production. The breeding of high L-lysine-producing strain Au112 is one of the outstanding examples of this approach. It is a homoserine auxotroph with AEC, TA double metabolic analogue resistant markers. The yield reaches 100 g/l. Besides, the citric acid-producing organism Aspergillus niger, Co827, its productivity reaches the advanced level in the world, is also the result of a series mutations especially with $^60Co{\gamma}$-radiation. The thermostable .alpha.-amylase producing strain A 4041 is the third example. By combining physical and chemical mutations, the strain A 4041 becomes an asporogenous, catabolite derepressed mutant with rifamycin resistant and methionine, arginine auxotroph markers. The .alpha.-amylase activity reaches 200 units/ml. The fourth successful example of mutation in strain improvement is the glucoamylase-producing strain Aspergillus niger SP56, its enzyme activity is 20,000 units/ml, 4 times of that of the parental strain UV-11. Recently, recombinant DNA approach provides a worthwhile alternative strategy to industrial strain improvement. This technique had been used by us to increase the thermostable .alpha.-amylase production and on some genetic researches.

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Isolation of $NH_4^+$-Tolerant Mutants of Actinobacillus succinogenes for Succinic Acid Production by Continuous Selection

  • Ye, Gui-Zi;Jiang, Min;Li, Jian;Chen, Ke-Quan;Xi, Yong-Lan;Liu, Shu-Wen;Wei, Ping;Ouyang, Ping-Kai
    • Journal of Microbiology and Biotechnology
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    • 제20권8호
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    • pp.1219-1225
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    • 2010
  • Actinobacillus succinogenes, a representative succinicacid-producing microorganism, is seriously inhibited by ammonium ions, thereby hampering the industrial use of A. succinogenes with ammonium-ion-based materials as the pH controller. Therefore, this study isolated an ammonium-ion-tolerant mutant of A. succinogenes using a continuous-culture technique in which all the environmental factors, besides the stress (ammonium ions), were kept constant. Instead of operating the mutant-generating system as a nutrient-limited chemostat, it was used as a nutrient-unlimited system, allowing the cells to be continuously cultured at the maximum specific growth rate. The mutants were isolated on agar plates containing the acid-base indicator bromothymol blue and a high level of ammonium ions that would normally kill the parent strain by 100%. When cultured in anaerobic bottles with an ammonium ion concentration of 354 mmol/l, the mutant YZ0819 produced 40.21 g/l of succinic acid with a yield of 80.4%, whereas the parent strain NJ113 was unable to grow. When using $NH_4OH$ to buffer the culture pH in a 3.0 l stirredbioreactor, YZ0819 produced 35.15 g/l of succinic acid with a yield of 70.3%, which was 155% higher than that produced by NJ113. In addition, the morphology of YZ0819 changed in the fermentation broth, as the cells were aggregated from the beginning to the end of the fermentation. Therefore, these results indicate that YZ0819 can efficiently produce succinic acid when using $NH_4OH$ as the pH controller, and the formation of aggregates can be useful for transferring the cells from a cultivation medium for various industrial applications.

Bacillus subtilis ATP 조해(阻害) Ribonuclease에 관한 연구 (ATP-Inhibited Ribonuclease of Bacillus subtilis)

  • 이택수
    • Applied Biological Chemistry
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    • 제18권3호
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    • pp.167-176
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    • 1975
  • ATP-저해 ribonuclease는 Bacillus subtilis와 같은 Bacillus속에서만 발견 되는 것으로서 이들 효소의 생리적 역활을 규명할 목적으로 Bacillus subtilis 균주를 사용하여 ATP저해성 negative ribonuclease변이주의 취득을 시도하고 선정된 균주가 생산하는 ribonuclease의 정제 및 몇 가지 성질에 대하여 실험한 결과는 아래와 같다. 1. Bacillus subtilis로 부터 ATP-저해 ribonuclease negative mutant의 취득을 시도한 결과 시험된 1817주의 균중에서 101균주가 변이주주로 선정 되었다. 2. 수개의 개별적인 column chromatography에 의하여 당균주가 생산하는 ATP-저해성 ribonuclease의 정제를 시도한 결과 DEAE-Sephadex A-50 column chromatography을 이용한 경우는 30배의 정제 효과와 99%의 회수율을 나타냈고 Sephadex G-75 column의 경우는 20배의 정제 효과와 98%의 회수율을 각각 나타냈다. 3. pH 5침전, 유안염석, Sephadex G-75 및 CM Sephadex를 연속적으로 통과시켜 당효소에 대한대량정제 시험을 시도한 결과 최초의 step(crude extract) 과정에 비하여 60배의 정제효과를 나타냈다. 4. 본정제 효소액에 대하여 전기영동을 실시한 결과 비정제 효소액에 비하여 매우 감소된 수의 담백 pattern을 나타냈다. 5. 당균주가 생산하는 ATP저헤 ribonuclease는 single stranded RNA를 분해하여 2',3'-cyclic AMP, 2',3'-cyclic CMP, 2',3'-cyclic GMP, 2',3'-cyclic UMP와 몇종의 미지물을 생성하였고 또한 본효소는 double stranded RNA를 분해하지 않었다.

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The N-Terminal α-Helix Domain of Pseudomonas aeruginosa Lipoxygenase Is Required for Its Soluble Expression in Escherichia coli but Not for Catalysis

  • Lu, Xinyao;Wang, Guangsheng;Feng, Yue;Liu, Song;Zhou, Xiaoman;Du, Guocheng;Chen, Jian
    • Journal of Microbiology and Biotechnology
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    • 제26권10호
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    • pp.1701-1707
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    • 2016
  • Lipoxygenase (LOX) is an industrial enzyme with wide applications in food and pharmaceutical industries. The available structure information indicates that eukaryotic LOXs consist of N terminus β-barrel and C terminus catalytic domains. However, the latest crystal structure of Pseudomonas aeruginosa LOX shows it is significantly different from those of eukaryotic LOXs, including the N-terminal helix domain. In this paper, the functions of this N-terminal helix domain in the soluble expression and catalysis of P. aeruginosa LOX were analyzed. Genetic truncation of this helix domain resulted in an insoluble P. aeruginosa LOX mutant. The active C-terminal domain was obtained by dispase digestion of the P. aeruginosa LOX derivative containing the genetically introduced dispase recognition sites. This functional C-terminal domain showed raised substrate affinity but reduced catalytic activity and thermostability. Crystal structure analyses demonstrate that the broken polar contacts connecting the two domains and the exposed hydrophobic substrate binding pocket may contribute to the insoluble expression of the C terminus domain and the changes in the enzyme properties. Our data suggest that the N terminus domain of P. aeruginosa LOX is required for its soluble expression in E. coli, which is different from that of the eukaryotic LOXs. Besides this, this N-terminal domain is not necessary for catalysis but shows positive effects on the enzyme properties. The results presented here provide new and valuable information on the functions of the N terminus helix domain of P. aeruginosa LOX and further improvement of its enzyme properties by molecular modification.

Morphological Traits of S598A Sweetpotato as an Industrial Starch Crop

  • Kim, Kyung-Moon;Kim, Ji-Yeon;Kim, Jung-Il
    • 한국작물학회지
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    • 제54권4호
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    • pp.422-426
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    • 2009
  • Sweetpotato is one of the important starch crops, current more considered as an industrial crop rather than food because it has higher starch content (over 80% of biomass), it is used for bio resources for industrial area. In this study, we generated S598A (a mutant gene of oat phytochrome A) sweetpotato plant using Agrobacterium-transformation method. Morphological characteristics of S598A plant were compared with the wild type sweetpotato, S598A had darker green leaves, increased chlorophyll content higher than to two-fold, delayed leaf senescence, shorter plant height (60% shorter than that of the wild type), more number of leaves and petioles about 1.8-fold, shorter petiole length (30% shorter), 1.2-fold more branches and 1.6-fold thicker stem diameters. From this study, S598A plants with such phenotypic characteristics might be able to use the solar energy efficiently, to have increased tolerance to biotic and abiotic stresses and finally to increase productivity (not only starch yield but also root biomass yield). S598A sweetpotato lines are under field trials.

열내성 Cellobiose 2-epimerase를 발현하는 대장균의 고정화담체를 이용한 락툴로오스의 생산방법 (Lactulose Production Using Immobilized Cells Including Thermostable Cellobiose 2-epimerase)

  • 박아름;구봉성;김진숙;김은정;이현철
    • 한국미생물·생명공학회지
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    • 제44권4호
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    • pp.504-511
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    • 2016
  • 락툴로오스는 기존에 화학적인 이성화법을 통해 생산해왔던 기능성 당으로서 프로바이오틱스나 장내균총 개선을 위한 의약품으로 활용되어 왔다. 최근 락툴로오스 화학전환법의 단점인 촉매제거와 부산물제거 에너지손실등의 문제를 해결할 수 있는 생물촉매를 이용한 락툴로오스 전환법이 대두되었다. 본연구에서는 유당의 낮은 용해도와 락툴로오스의 효율적전환을 위해 최적의 효소를 선별하여 무작위 돌연변이법으로 유전자를 개량하여 열내성이 $75^{\circ}C$까지 증진되고 활성이 1.3배 향상된 효소를 선별하였다. 이 효소를 정제하여 사용하는 대신 본 연구에서는 과량 발현시킨 대장균을 Ca-alginate로 고정화하여 $70^{\circ}C$에서 200 g/l의 유당과 회분식으로 반응시켜 43%의 전환 수율을 확인하였다. 반복회분식 실험에서 고정화된 담체는 비교적 안정적이었으며 4회 반복반응 후에도 80% 이상의 활성을 유지하고 있었다. 산업적인 방법을 개발하기 위해 고정화 담체를 이용한 반응기의 운전 최적화와 담체의 안정화를 증진시키는 추가적인 연구가 필요하지만, 본 연구에서는 열내성 특성을 이용하여 정제된 효소가 아닌 효소를 발현하는 세포자체를 고정화 시킴으로써 경제성있는 생산에 대한 방법론을 제시하였다.

Cold-Adapted and Rhizosphere-Competent Strain of Rahnella sp. with Broad-Spectrum Plant Growth-Promotion Potential

  • Vyas, Pratibha;Joshi, Robin;Sharma, K.C.;Rahi, Praveen;Gulati, Ashu;Gulati, Arvind
    • Journal of Microbiology and Biotechnology
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    • 제20권12호
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    • pp.1724-1734
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    • 2010
  • A phosphate-solubilizing bacterial strain isolated from Hippophae rhamnoides rhizosphere was identified as Rahnella sp. based on its phenotypic features and 16S rRNA gene sequence. The bacterial strain showed the growth characteristics of a cold-adapted psychrotroph, with the multiple plant growth-promoting traits of inorganic and organic phosphate solubilization, 1-aminocyclopropane-1-carboxylate-deaminase activity, ammonia generation, and siderophore production. The strain also produced indole-3-acetic acid, indole-3-acetaldehyde, indole-3-acetamide, indole-3-acetonitrile, indole-3-lactic acid, and indole-3-pyruvic acid in tryptophan-supplemented nutrient broth. Gluconic, citric and isocitric acids were the major organic acids detected during tricalcium phosphate solubilization. A rifampicin-resistant mutant of the strain exhibited high rhizosphere competence without disturbance to the resident microbial populations in pea rhizosphere. Seed bacterization with a charcoal-based inoculum significantly increased growth in barley, chickpea, pea, and maize under the controlled environment. Microplot testing of the inoculum at two different locations in pea also showed significant increase in growth and yield. The attributes of cold-tolerance, high rhizosphere competence, and broad-spectrum plant growth-promoting activity exhibited the potential of Rahnella sp. BIHB 783 for increasing agriculture productivity.