• 제목/요약/키워드: Stationary phase

검색결과 775건 처리시간 0.034초

사과주(酒) 산막효묘(産膜酵母) Hansenula beijerinckii FY-5 의 소수성(疏水性)과 산막성(産膜性)과의 관련성(關聯性) (Relationship between Hydrophobicity and Pellicle Formation in a Film Strain of Hansenula beijerinckii FY-5 Isolated from Apple Wine)

  • 송형익;정기택
    • 한국식품과학회지
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    • 제17권3호
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    • pp.203-207
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    • 1985
  • 저장사과주에서 분리(分離) 동정(同定)한 산막효모(産膜酵母) Hansenula beijerinckii FY-5의 소수성(疎水性)과 피막형성(皮膜形成)과의 관계(關係)를 조사하였다. 비(非)이온계(系) 계면활성제(界面活性劑) 첨가에 의해 균생육(菌生育)은 가능(可能)하지만 피막(皮膜)이 전혀 형성(形成)되지 않으며 소수도(疎水度)도 크게 낮아지는 사실로 미루어 볼때, 피막형성(皮膜形成)에는 효모세포(醉母細胞)를 배지표면(表面)에 보존(保持)시키는 어떤 인자(因予)가 요구되며 그 인자(因子)가 바로 효모세포표면(酵償細胞表面)외 소수성(疎水性)이 아닌가 생각된다. 산막성효모(産膜性酵母)에 있어서는 소수도(疎水度)가 클수록 피막형성(皮膜形成)이 왕성하였으나 비산막성효모(非産膜性酵母)는 대체로 소수도(疎水度)가 낮았다. 탄소원이 에타놀일때 소수도(疎水度)가 높았으며 pH의 상승에 따라 소수도(疎水度)는 감소(減少)하는 경향이었다. 배양기간별로는 균생육(菌生育)과 더불어 소수도(疎水度)도 비례적으로 증가하여 정상기(正常期)에 최대치를 보였다.

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Lactobacillus casei subsp. 및 Streptococcus faecium이 생산한 항균성물질의 성상 (Characteristics of the antibacterial substances produced by Lactobacillus casei subsp. and Streptococcus faecium)

  • 강경구;마점술
    • 대한수의학회지
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    • 제33권3호
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    • pp.393-406
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    • 1993
  • Antibacterial substances produced by Lactobacillus casei subsp. and Streptococcus faecium were examined for its antibacterial effects against some pathogenic bacteria. They were partially purified with ammonium sulfate precipitation, methanol-acetone extraction, G-50 gel filtration and examined its characteristics. When L casei subsp. and Str faecium were cultivated in MRS broth, stationary phase of L casei is until 24 hours and Str faecium is 20 hours. pH change of the cultured medium was both decreased after 12 hours and then constant at pH 4.5~4.6 after 28 hours. MRS broth culture fluids of L casei subsp. and Str faecium appeared the antibacterial effects by the spot-on-the-lawn method against ETEC, Sal pullorum and Sta aureus. Culture filtrates of L casei subsp. and Str faecium also appeared the antibacterial effects by the disc diffusion method. Culture filtrates of L casei sub. rhamnosus 7469 produced 0.032M of lactic acid and 0.01M of acetic acid. Str faecium 27273 also produced 0.027M of lactic acid and 0.01M of acetic acid. Protein concentrations of culture filtrates produced by L casei sub rhamnosus 7469 and Str faecium 27273 was $495{\mu}g/m{\ell}$ and $594{\mu}g/m{\ell}$, respectively. Antibacterial substances which are partially purified by ammonum sulfate precipitation, methanol-acetone extraction and G-50 gel filtration inhibit the growth of ETEC, Sal pullorum and Sta aureus. Characteristics of purified antibacterial substances was examined. Its molecular weight was about 31Kd, stabilized at $100^{\circ}C/20min.$ and some of proteolytic enzyme treatment.

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GC를 이용한 극성용매의 분석방법 개발 연구 (Study on Development of Analytical Method for Polar Solvents by GC)

  • 오도석;김성화;이슬;황경철
    • 한국산업보건학회지
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    • 제26권1호
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    • pp.20-29
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    • 2016
  • Objectives: The purpose of this study is to simplify and standardize analytical method of polar solvents(methanol, isopropanol, n-butanol, acetone, methylene chloride and MIBK) in the working environmental by GC. Because NIOSH methods are various and complicated. Methods: The method is using the same stationary phase(5% phenyl 95% dimethylpolysiloxane), absorbent(silica gel) and desorption solvent(DMSO) for above 6 solvents. For the 6 solvents desorption efficiency, calibration curve, and limit of detection were studied Results: As the results, 6 solvents{2 groups ; first group(methanol/isopropanol/butanol) and second group(acetone/methylene chloride/MIBK)} could be separated and quantified within 10 minutes. Desorption efficiency from silica gell of 6 solvents using dimethylsulfoxide(DMSO) was methanol 86.2%, isopropanol 103.2%, n-butanol 101.8%, acetone 98.2%, methylene chloride 103.9% and MIBK 106.2% in the range of 0.2, 0.5, 2.0 times of TWA, consequently, satisfied NIOSH estimation level(beyond 75%). Correlation coefficient(r)in the range of 0.2~2.0 times of TWA, was above 0.999 for 6 solvent. LOD(mg/DMSO ml) using calibration curve in the range of 0.2~2 times of TWA was methanol 0.11, isopropyl alcohol 0.20, n-butanol 0.03, acetone 0.50, methylene chloride 0.05, MIBK 0.04 respectably. Conclusions: This method can be used at the sampling and analytical method for polar solvents by GC. Also, will be able to be applied with NIOSH methods.

Overexpression of the spr D Gene Encoding Strptomyces griseus Protease D Stimulates Actinorhodin Production in Streptomyces lividans

  • Choi, Si-Sun;Chi, Won-Jae;Lee, Jae-Hag;Kang, Sang-Soon;Jeong, Byeong-Chul;Hong, Soon-Kwang
    • Journal of Microbiology
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    • 제39권4호
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    • pp.305-313
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    • 2001
  • The spr D gene encoding Strptomyces griseus protease D(SGPD); a chymotrypsin-like proteae, was cloned from Strptomyces griseus IFO13350 and sequence. Most of the amino-acid sequence deduced from the nucleotide sequence is idential to that Strptomyces griseus IMRU3499 except that one amino acid has been deleted and Trp 369 has been substituted into Cys369 in the SGPD from S. griseus IFO13350 without affecting the protease activity. The spr D gene was overexpressed in Streptomyce liv-idans TK24 as a heterologous host. Various media with different compositions were also used to max-imize the productivity of SGPD inthe heterologous host. The SGPD productivity was best when the transformant S. lividans TK24 was cultivated in R2YE medium. The relative chymotrypsin activity of the culture broth measured with an artificial chromogenic substrate, N-scuccinyl-ala-ala-pro-phe-p-nitroanilide, was 16 units/ml. A high level of SGPD was also produced in YEME and SAAM medial but it was relatively lower that in R2YE medium and negligible amounts of SGPD were produced in GYE, GAE and Benedict media. The growth of S. lividans reacted the maximum level of cell mass at days 3 and 4 of the culture, but SGPD production started in the stationary phase of cell growth and kept increase in till the 10$^{th}$ day of culture in R2YE and YEME medium, but in GYE media the productivity reached maximum level at 8days of cultivation. The introduction of the spr D gene into S. lividans TK24 triggered biosyntheis of the pigmented antibiotic , actinorhodin, which implies some protease may paly a very improtant role in secondary-metabolite formation in sStreptomyces.

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GABA 함량이 높은 청국장을 발효하는 균주의 분리 및 동정 (Isolation and Identification of GABA-producing Microorganism from Chungkookjang)

  • 맹소연;김은아;이가영;김로의;황대연;손홍주;김동섭
    • 생명과학회지
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    • 제23권1호
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    • pp.102-109
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    • 2013
  • 전통적인 방법으로 제조된 청국장으로부터 우수한 발효 균주들을 분리하여 재래식으로 청국장을 제조하고, 제조된 청국장의 생리활성 물질인 GABA를 유지 및 보강하면서 품질을 향상시키기 위하여 청국장 발효능이 뛰어난 종균을 찾아 분리하였다. 분리된 균주들 가운데 GABA의 함량이 높은 청국장을 생산하는 MC 31을 실험균주로 선택하였고 API Kit와 16S rDNA sequence를 통하여 Bacillus subtilis MC 31로 명명하였다. B. subtilis MC 31의 최적배지와 온도, 시간을 찾아본 결과 LB 배지에서 $37^{\circ}C$, 24시간이 가장 높은 생육을 나타내었다. GABA 생산에 적합한 발효 온도와 시간을 조절하여 최적 조건을 찾아본 결과 B. subtilis MC 31는 $40^{\circ}C$에서 72시간에 가장 많은 GABA를 생산하였다.

State detection of explosive welding structure by dual-tree complex wavelet transform based permutation entropy

  • Si, Yue;Zhang, ZhouSuo;Cheng, Wei;Yuan, FeiChen
    • Steel and Composite Structures
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    • 제19권3호
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    • pp.569-583
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    • 2015
  • Recent years, explosive welding structures have been widely used in many engineering fields. The bonding state detection of explosive welding structures is significant to prevent unscheduled failures and even catastrophic accidents. However, this task still faces challenges due to the complexity of the bonding interface. In this paper, a new method called dual-tree complex wavelet transform based permutation entropy (DTCWT-PE) is proposed to detect bonding state of such structures. Benefiting from the complex analytical wavelet function, the dual-tree complex wavelet transform (DTCWT) has better shift invariance and reduced spectral aliasing compared with the traditional wavelet transform. All those characters are good for characterizing the vibration response signals. Furthermore, as a statistical measure, permutation entropy (PE) quantifies the complexity of non-stationary signals through phase space reconstruction, and thus it can be used as a viable tool to detect the change of bonding state. In order to more accurate identification and detection of bonding state, PE values derived from DTCWT coefficients are proposed to extract the state information from the vibration response signal of explosive welding structure, and then the extracted PE values serve as input vectors of support vector machine (SVM) to identify the bonding state of the structure. The experiments on bonding state detection of explosive welding pipes are presented to illustrate the feasibility and effectiveness of the proposed method.

홍화씨 분말 첨가가 김치의 품질에 미치는 영향 (Effects of Safflower Seed Powder on the Quality Characteristics of Kimchi)

  • 박우포;박규동;엄현섭
    • 한국식품저장유통학회지
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    • 제9권2호
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    • pp.200-204
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    • 2002
  • 김치 담금시부터 숙성 13일경까지 홍화씨 분말을 첨가한 시험구들은 대조구보다 대체적으로 낮은 pH를 나타내었으며, 그 이후에는 시험구간에 큰 차이를 나타내지는 않았다. 숙성 2일까지는 적정산도가 큰 차이를 나타내지 않았으나 그 이후 13일경까지는 대조구가 가장 낮은 값을 나타내었으며, 홍화씨 분말의 첨가량이 많을수록 높은 값을 나타내었다. 숙성 20일 이후에는 시험구간에 큰 차이를 나타내지는 않았다. 김치가 숙성되는 동안 환원당 함량은 지속적으로 감소하여 숙성 20일에 최저 함량을 보였으며, 홍화씨 분말을 2% 첨가한 시험구가 대체적으로 낮은 값을 나타내었다. 김치 담금 후 숙성 5일 사이에 총균수와 유산균수가 급격하게 증가하였으며, 대조구는 숙성 15일에 최대값을 나타내었으나 홍화씨 분말을 첨가한 시험구는 숙성 10일에 최대 값을 나타내었다. 관능검사 결과 홍화씨 분말을 3% 첨가한 시험구를 제외한 시험구들은 냄새 및 맛에 있어서 대조구와 유의적인 차이를 나타내지는 않았다.

폐섬유자원의 발효공학적 이용에 관한 연구 (제오보) 분리균 Cellulomonas속 균주의 이용성 (Studies on the Fermentative Utilization of Cellulosic Wastes. (Part V) Utilization of Cellulomonas sp.)

  • 심기환;성낙기;윤한대
    • 한국미생물·생명공학회지
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    • 제5권1호
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    • pp.24-28
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    • 1977
  • 비교적 효율적으로 이용되고 있지 않는 섬유성물질의 이용성을 높이고 섬유소 자화세균에 의한 섬유소 단세포단백을 생산할 목적으로 전보에서 분리, 동정한 Collulomonas flavigena GFB 24-1의 몇 가지 균학적 성질을 통한 이용성을 검토한 결과를 요약하면 다음과 같다. 1. 섬유질 자화세균 생육배지에서 배양한 결과 pH 7.0에서 50시간 배양하였을 때 균체증식이 가장 좋았고, 배양시 유리되는 단백질은 배양중 시간이 경과됨에 따라 증가하였다. 2. Cellulolytic activity는 pH 5~7에서 40~50시간, 배양하였을 때 가장 좋았다. 4. 생육배지에서 배양시 기질의 농도의 증가에 따라 6%까지는 균체증식이 직선적으로 증가하였으며 8%까지는 완만하게 증가하다가 9~10%농도에서는 감소하였다. 5. NaOH 처리한 볏짚은 기질로 하여 진탕 flask에서 배양한 결과 48기산 배양하였을 때 균체증식이 10.6mg/ml로써 가장좋았다.

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Heterologous Expression of Streptomyces albus Genes Linked to an Integrating Element and Activation of Antibiotic Production

  • Kwon, Hyung-Jin;Lee, Soon-Youl;Hong, Soon-Kwang;Park, Uhn-Mee;Suh, Joo-Won
    • Journal of Microbiology and Biotechnology
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    • 제9권4호
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    • pp.488-497
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    • 1999
  • Probing Streptomyces albus ATCC 21838 chromosomal DNA with a proline tRNA sequence resulted in an isolation of a putative integrating element in the 6.4-kb EcoRI fragment. It was found that Streptomyces lividans TK-24 transformed with a cloned DNA fragment on a multicopy plasmid, produced a higher level of spore pigment and mycelial red pigment on a regeneration agar. Furthermore, the transformant S. lividans TK-24 produced a markedly increased level of undecylprodigiosin in a broth culture. A nucleotide sequence analysis of the cloned region revealed several open reading frames homologous to the integrases of integrating plasmids or temperate bacteriophages, signal-transducing regulatory proteins with a conserved ATP-binding domain, oxidoreductases ($\beta$-ketoacyl reductase), and an AraC-like transcriptional regulator. To examine the effect on antibiotic production, each coding region was overexpressed separately from the other genes in the region in S. lividans TK-24 with; pJHS3044 for the expression of the signal-transducing regulatory protein homologue, pJHS3045 for the homologue of oxidoreductase, and pJHS3051 for the homologue of the AraC-like transcriptional regulator. Phenotypic studies of S. lividans TK-24 strains harboring plasmids for the overexpression of individual genes suggested the following effects of the genes on antibiotic production: The oxidoreductase homologue stimulated the production of actinorhodin and undecylprodigiosin, which was influenced by the culture conditions; the homologue of the AraC-like transcriptional regulator was the most effective factor in antibiotic production within all the culture conditions tested; the signal-transducing regulatory protein homologue repressed the effect due to the homologue of the AraC-like transcriptional regulator, however, the antibiotic production was derepressed upon entering the stationary phase.

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Cellulosimicrobium sp. 분리균의 Hemicellulases 생산성과 효소특성 (Production and Properties of Hemicellulases by a Cellulosimicrobium sp. Isolate)

  • 윤기홍
    • 한국미생물·생명공학회지
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    • 제39권3호
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    • pp.252-258
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    • 2011
  • 탄소원으로 palm kernel meal(PKM)과 밀기울을 함유한 배지에서 농후배양하여 작물 재배 토양으로부터 xylan과 locust bean gum(LBG)에 대한 분해활성이 있는 균을 분리하였다. 분리균 YB-1107의 16S rDNA 서열이 Cellulosimicrobium 속 균주와 유사도가 높은 균주로 판명되었다. 분리균의 mannanase는 LBG와 PKM에 의해 생산성이 증가된 반면에 xylanase는 oat spelt xylan과 밀기울에 의해 생산성이 증가되었다. Mannanase는 0.7% PKM을 첨가한 배지, xylanase는 1% 밀기울을 첨가한 배지에서 각각 최대 생산성을 보였으며 모두 정지기에서 생산이 되었다. 분리균의 배양상등액은 $55^{\circ}C$와 pH 6.5에서 mannanase의 최대활성을 보였으며, $65^{\circ}C$와 pH 5.5에서 xylanase의 최적반응 활성을 나타냈다. Mannanase에 의해 분해된 LBG와 xylanase에 의해 분해된 xylan으로부터 각각 올리고당이 관찰되었으며, 또한 이들 효소는 밀기울과 미강도 분해하여 올리고당으로 전환하는 것으로 확인되었다.