• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    1530771 Microbiological testing MCDONNELL DOUGLAS CORP 6 Jan 1977 [3 May 1976] 388/77 Heading C6F A composition for selectively identifying Escherichia coli (E. coli) for use with an automated microbial analyzer comprises: (1) lactose and L-arabinose as sources of nutrients which are fermented by E. coli, (2) reduced Aniline Blue to indicate the presence of E. coli organisms (colourless to blue at pH 6.8-7), (3) the combination of coumaric acid (preferably the para compound), 3,4-dihydroxybenzoic acid and saponin as the means for inhibiting the growth of other coliform-like organisms, principally Klebsiella, which normally give positive results in tests for E. coli and optionally, (4) bile salts to inhibit the growth of Gram-positive organisms generally. A solution of the ingredients of the composition, together with other, conventional constituents, in stated amounts in distilled water (pH 7À5) is loaded into the wells of a urine screening card and freeze-dried in situ and the wells taped to protect the media prior to use. The medium will be rehydrated when a sample of urine is added to it for testing.
    公开号:SU741805A3
    申请号:SU772464948
    申请日:1977-03-28
    公开日:1980-06-15
    发明作者:Вэйн Лэнхэм Джеймс；Дуглас Родгерс Грегори；Чарльз Мейер Майкл
    申请人:Макдоннел Дуглас Корпорейшн (Фирма)；
    IPC主号:
    专利说明:

    (54) NUTRIENT FOR ESCHERiCHfA COli
    I
    This invention relates to the field of microbiology and can be used to identify microorganisms.
    A known nutrient medium for the identification of Escherichia cOT containing nutrient base, lactose, indicator, gram-positive microflora inhibitor and water 1.
    However, the known medium does not provide rapid identification of Escherichia coli.
    The aim of the invention is to accelerate the identification of Escherichia col i.
    This goal is achieved by the fact that the medium additionally contains arabinose, p-coumaric acid, dihydroxybenzoic acid, saponin, extract, it contains gelizat as a nutrient base, aniline blue as indicator, and bile salts as an inhibitor of gram-positive microflora. the following ratio of components, g / l:
    Gelizat
    5.0 - 6.0 4.0 - 6.0 Lactose
    4.0 - 6.0 Arabinose 0.75 - 1.25 Yeast Extract
    IDENTIFICATION
    - 1.25
    0.75
    Saponin - 1.5 0.05
    p-Kumarov acid
    Dihydrobenzoic
    0.05 - 1.5
    acid
    1.5 - 4.5
    Bilious Sun, 15 - 35 (ml)
    Aniline blue
    Water Rest
    The proposed medium contains sources of sugar that are selectively fermented.
    10 bacteria with the formation of acids, and also contains an indicator of pH-sensitive aniline blue, the color of which turns into blue in an acidic environment. The medium also contains inhibitors for other gram-negative or19 ganisms, as an example, for labs i na. The combination of inhibitors contains coumarin acid, 3,4-dihydroxybenzoic acid and saponin.
    20
    This combination inhibits Klebsiella to allow Escherichia CoP to grow.
    The medium contains also surfactants and inhibitors for gram-positive organisms. Nutrient sources are also used for the proposed medium (1x growth of Escherichia coli, a biological pH indicator that reacts to the acid formed by E.coli i, and a combination of p-coumaric acid, saponin and 3,4-dihydroxybenzoic acid to inhibit Klebsiella growth , also other inhibitors to inhibit the growth of gram-positive microorganisms. Most strains of E. col i ferment lactose to form acid, o-ara & 1, use sweat in detecting media. A suitable substitute for helsate is trypticase, finto and psiyshpton. Bile salt mixtures are used to inhibit the growth of gram-positive organisms.These mixtures contain extractive substances of bile and are a mixture of surface-active substances that inhibit gram-positive organisms. Another suitable surfactant is taurochloric acid. 3,4-dihydroxybenzoic acid, saponin and p-coumaric acid are used to inhibit the growth of Klebsiella and other E. coli-like organisms. O- and m-coumaric acid may be used. The preferred indicator for the medium is aniline. As a source of vitamins, add yeast or other suitable biological extract in the amount of 0.95-1.05 g / l. Before using the medium, its pH should be 7.5. The medium is prepared as follows. Mix 0.2 g of p-coumaric acid, 0.2 g of 3,4-dihydroxybenzoic acid with 3 1 n. AOH / 100 ml of medium and 1/4 of the required volume of distilled water give 100 ml of double strength medium. 1 This mixture is heated to dissolve all solids. The solution is made up to 95 ml with distilled water and 1.0 g of gelisate, 1.0 g of lactose, 1.0 g of L-arabinose, 0.6 g of a mixture of bile salts and 0.2 g of yeast extract are added to it. The pH is adjusted to 6.2 and 5 ml of indicator is added - reduced aniline blue with OD g saponin. Check and adjust to 7.2 by addition of base. The solution is sterilized by filtration, placed in a stern container and labeled. Nutrient medium is used as follows. The medium is loaded into the wells of the urine analysis cards, dried at a temperature below 0 ° C and the cards are coated to protect the medium. The grooves are filled with half the volume of the medium. Then, when the remaining volume of depressions is filled with a urine sample, the medium is again hydrated to a normal single strength concentration at which it works. This medium can detect EiColi concentrations of 10 cells / ml in 12 hours. A longer time is required at lower concentrations. The proposed environment accelerates the identification of Escherichia coli. Formulas of the invention Nutrient medium for identification of Escherichia coli, containing nutrient base, lactose, bladder, gram-susceptible microflora inhibitor and water, characterized in that, in order to accelerate the identification of Escheridiia coli, it additionally contains arabinose, p-coumaric acid , dihydroxybenzoic acid, saponin, yeast extract, as a nutrient base, it contains gelizat, aniline blue as an indicator, and as an inhibitor of gram-positive microflora - bile salts and components, g / l: Gelizat 5,0 - 6,0 Lactose 4,0 - 6,0 Arabinose 4,0-6,0 Yeast extract 0.75 - 1.25 Saponin 0.75 - 1.25 p-Kumphova acid 0.05 - 1.5 Dihydroxybenzoic acid 0.05 - 1.5 Bile salts1.5 - 4.5 Aniline blue15 - 35 (ml) WaterOstal. Sources of information taken into account in the examination 1. Handbook of microbiological and virological research methods. Ed. M. O. Birger. M., Medicine, 1973, p. 58.
    权利要求:
    Claims (1)
    [1]
    Claim
    20 !
    The nutrient medium for the identification Esche * rich fa coli, comprising a nutrient base, lactose, indicator, inhibitor of Gram-positive microflora and water, wherein 25 Jasia in that, in order to accelerate the identification of Escherichia coli, it further comprises arabinose, p-coumaric acid, dihydroxybenzoic acid, saponin, yeast extract, it contains gelizate as a nutrient base, aniline blue as an indicator, and bile salts as an inhibitor of gram-positive microflora in the following ratio of
    tov, g / l: z5 Gelizat 5.0 - 6.0 Lactose 4.0 - 6.0 Arabinose 4.0 - 6.0 Yeast extract 0.75 - - 1.25 Saponin 0.75 - 1.25 p-Coumaric acid, dihydroxybenzo, other 0.05 - 1.5 acid 0.05 - 1.5 Bile salts 1,5 - 4,5 Aniline blue fifteen - -35 (ml) Water Rest.
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    同族专利:
    公开号 | 公开日
    IL51238D0|1977-03-31|
    CA1060764A|1979-08-21|
    GB1530771A|1978-11-01|
    ZA7736B|1977-11-30|
    ATA103877A|1978-09-15|
    DD129490A5|1978-01-18|
    FR2350394A1|1977-12-02|
    DK84677A|1977-11-04|
    AU2137777A|1978-07-27|
    JPS52134084A|1977-11-09|
    ES456306A1|1978-05-01|
    US4072572A|1978-02-07|
    BE851877A|1977-08-29|
    DE2708356B2|1978-09-21|
    LU76851A1|1977-09-12|
    FI770502A|1977-11-04|
    JPS5525839B2|1980-07-09|
    DE2708356C3|1979-05-31|
    IT1074839B|1985-04-20|
    NL7701900A|1977-11-07|
    NO770657L|1977-11-04|
    DE2708356A1|1977-11-10|
    FR2350394B1|1980-02-01|
    SE7701602L|1977-11-04|
    BR7700942A|1977-10-18|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US3825474A|1972-06-22|1974-07-23|P Cooper|Proteus resistant agar culture media|US4144133A|1977-08-25|1979-03-13|J. K. And Susie L. Wadley Research Institute And Blood Bank|Fungal growth media|
    IL54621D0|1977-08-29|1978-07-31|Mc Donnell Douglas Corp|E. coli sensitivity broth|
    US4279995A|1979-12-03|1981-07-21|Mcdonnell Douglas Corporation|Selective salmonella carbohydrate and medium constructed therefrom|
    NL8003140A|1980-05-29|1982-01-04|Thomassen & Drijver|METHOD AND APPARATUS FOR MANUFACTURING A BUS ROPE AT LEAST AT LEAST END INCLUDING AN OUTWARD DIRECTIVE FLANGE AND CONNECTED CIRCULAR TIGHTENING|
    AT403054B|1996-03-04|1997-11-25|Stauffer Elisaweta Mag|METHOD AND DEVICE FOR DETERMINING COLIFORMER AND FECALCOLIFORM NUCLEES IN WATER|
    US8211657B2|2002-04-29|2012-07-03|The Board Of Trustees Of The University Of Arkansas|Capillary-column-based bioseparator/bioreactor with an optical/electrochemical detector for detection of microbial pathogens|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US05/682,651|US4072572A|1976-05-03|1976-05-03|E. coli detection broth for clinical use with automated microbial analyzer|
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