echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Biochemistry News > Biotechnology News > Sugar fermentation of microorganisms.

    Sugar fermentation of microorganisms.

    • Last Update: 2020-10-21
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    1, monosaccharine fermentation test
    (i), experimental principle
    monosaccharine fermentation is to add glucose, lactose or maltose and so on to protein water
    culture
    base, so that the final concentration of 0.75 to 1%. And add a certain amount of phenolic red indicator and small inverter, made of monosaccharide fermentation tube, inoculated bacteria cultured by 37 degrees C 18 to 24 hours, if you can break down the sugar-producing acid then phenolic red indicator from red yellow, if you can break down the acid has CO2 and H2 gas formation, small inverter is aggregated with air bubbles;
    (ii), experimental materials
    1. Bacteria: E. coli, typhoid 18 to 24 hours
    agar
    oblique culture.
    2.
    : glucose
    tube, lactose fermentation tube, etc.
    (iii) Experimental methods
    1. Typhoid and E. coli were inoculated in glucose and lactose fermentation tubes according to the liquid inoculation method.
    2. Incubate at 37 degrees C for 18 to 24 hours.
    3. Observations: Because some bacteria can break down a certain sugar acid, so the medium PH dropped below 7.0, in the phenolic red indicator, the medium color from red to yellow. The acid-producing person indicates that if a gas is produced at the same time, bubbles appear in the medium's small inverter tube, which is acid-producing and gas-producing, and is expressed as "⊕", without decomposition, the indicator does not change color, with "-" as the indication.
    (iv), experimental results
    thyroid Bacillus E. coli
    glucose and ⊕
    lactose - ⊕
    II, V-P (Voges-Proskauer) test
    (i), experimental principles
    some Bacteria such as gas-producing bacteria, decomposing glucose to produce acetone acid, acetone acid dehydration, the production of acetyl methyl methanol, in an alkaline environment is oxidized to diacetyl, and then combined with the culture base necide to produce red
    compounds
    , V-P test positive.
    (ii), experimental materials
    1. Bacteria: E. coli, gas-producing bacteria 18 to 24 hours agar slope culture.
    2. Culture: Glucose proteinwater culture.
    3.
    reagents
    : V-P reagents (40% potassium hydroxide solution (containing 0.3% crea acid) and 6% α-naphenol alcohol solution).
    (iii) the experimental method
    . 1. Inoculated against E. coli, the production of Bacillus gas in two glucosewater.
    2. After 48 hours of culture at 37 degrees C, remove 1 ml of KOH1ml and α-naphenol solution, shake well, and set aside
    tet tube
    rack for 5 to 15 minutes.
    (iv) and the experimental results
    the culture liquid became red as positive and the invaricose color was negative.
    3, methyl red test
    (i), experimental principle
    some bacteria such as E. coli and other decomposing glucose to produce acetone acid, and then decomposed into formic acid, acetic acid, lactic acid, etc., so that the culture base PH value dropped below 4.5, add methyl red instructions The agent is red, which is positive, if the amount of acid produced is small or the resulting acid is further converted into alcohol, aldehyde, gas and water, then the
    acid and alkali
    degrees of the culture is still above PH 6.2, the methyl red indicator is yellow, negative reaction.
    (ii), experimental materials
    . 1. Bacteria: E. coli, gas-producing bacteria 18 to 24 hours agar slope culture.
    2. Culture: Glucosewater culture.
    3. Reagents: Methyl Red Reagents.
    (iii) the experimental method
    . 1. E. coli and Bacillus gas produced were inoculated in two glucosewater mediums.
    2. Set 37 degrees C culture 2 to 3 days to remove, respectively, add methyl red reagents 2 to 3 drops, mix well, observe the results.
    (IV), the experimental results
    E. coli: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
    4. Sodium
    acid is the only carbon source and ammonium dihydrohydrogen
    phosphate is the only nitrogen source . General bacteria can use ammonium dihydrohydrogen phosphate as a nitrogen source, but not necessarilydecompose radon to obtain carbon source. For this reason, according to the possibility of using radonacid to identify bacteria, such as gassacs can be used as a carbon source, bacteria grow and reproduce, the formation of moss, decomposition of datesacid to produce alkaline carbonates, so that the culture pH rose to 7.0 Above, from green to dark blue, test positive for the use of radonate, while E. coli can not break down theacid, can not get carbon source, can not grow, sterile moss formation, the color of the culture base does not change, for the use of radonate test negative.
    (ii), experimental materials
    . 1. Bacteria: E. coli, gas-producing bacteria 18 to 24 hours agar slope culture.
    2. Culture base: acid slope.
    (iii) the experimental method
    . 1. E. coli, which produces Bacillus gas, was inoculated in two and acid ramp cultures.
    2. The results were observed after 24
    24
    at a temperature of 37 degrees C.
    (iv), the experimental results
    production of Bacillus gas: ( bacteria moss growth, culture base color change)
    E. coli: - (sterile moss growth, culture base unchanged color
    .
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.