Industrial Product From Microbial Process

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Transcript Industrial Product From Microbial Process

MIC 303 INDUSTRIAL AND ENVIRONMENTAL MICROBIOLOGY INDUSTRIAL PRODUCTS FROM MICROBIAL PROCESSES (CON’T)

Vinegar

an alcoholic liquid that has been allowed to sour.

“Vinegar” = the French word “vin” (wine), “aigre” (sour).

It is primarily used to flavor and preserve foods and as an ingredient in salad dressings and marinades.

also used as a cleaning agent.

Two way of production: i.

the microbial fermentation of alcohol ii. by the dilution of acetic acid Key equation: CH 3 CH 2 OH + O 2 → CH 3 CO 2 H + H 2 O

Types of vinegar

Malt vinegar Wine vinegar Other vinegars  Cider vinegar  Rice vinegar  Spirit vinegar Chemical synthesis of vinegar Balsamic vinegar Rice vinegar Balsamic vinegar

Microbes used

Key organism: Acetobacter (formerly known as Mycoderma), pertinent strains: Acetobacter aceti, Acetobacter pastorianus and Acetobacter hansenii Acetobacters are microscopic bacteria that live on oxygen bubbles.

Whereas the fermentation of grapes or hops to make wine or beer occurs in the absence of oxygen, the process of making vinegars relies on its presence.

Conversion generation of of ethanol to acetic aroma-active higher alcohols such as methyl butanol) acid is accompanied by secondary fermentation resulting in compounds (acetaldehyde, ethyl acetate and other esters and

Raw materials

Flavour: depends on the source of the alcohol.

Base materials: Herbs and fruit used to flavor vinegar.

Commonly used herbs include tarragon, garlic, and basil. Popular fruits include raspberries, cherries, and lemons.

Acetozym

In the vinegar factory, this process is induced by feeding acetozym nutrients into the tanks of alcohol.

Acetozym nutrients are manmade mother of vinegar in a powdered form.

It is a natural carbohydrate called cellulose. This film holds the highest concentration of acetobacters.

It is skimmed off the top and added to subsequent batches of alcohol to speed the formation of vinegar.

The Manufacturing Process The Generator Method

modern commercial production of vinegar.

submerged fermentation method.

These based on the goal of infusing as much oxygen as methods possible into are the alcohol product.

The Manufacturing Process The Submerged Fermentation Method

commonly used in the production of wine vinegars. Production plants are filled with large stainless steel tanks called acetators. The acetators are fitted with centrifugal pumps in the bottom that pump air bubbles into the tank in much the same way that an aquarium pump does. As the pump stirs the alcohol, acetozym nutrients are piped into the tank. The nutrients spur the growth of acetobacters on the oxygen bubbles. A heater in the tank keeps the temperature between 80 and 100°F (26-38°C).

The Manufacturing Process The Orleans Method

Slow process.

manufacture of high quality vinegars.

also called continuous method.

The Manufacturing Process

Natural Fermentation

Made easily by fermenting fresh sap into plastic or earthen jar until it becomes sour.

Then pack into plastic bottles and place under the heat of sun for few days.

PRODUCTION OF ANTIBIOTICS PENICILLIN

Antibiotics produced by Microorganisms

Antibiotic Producing microorganism

Cephalosporin

Chloramphenicol Streptomyces venezuelae

Erythromycin

Cephalosporium acrimonium Streptomyces erythreus

Griseofulvin Penicillin Streptomycin Tetracycline Gentamicin

Penicillium griseofulvin Penicillium chrysogenum Streptomyces griseus Streptomyces aureofaciens Micromonospora purpurea

Synthesis Pathway

 -ketoglutarate + AcCoA → homocitrate → L-α aminoadipic acid → L-Lysine + β-lactam The term "penam" is used to describe the core skeleton of a member of a penicillin antibiotic. This skeleton has the molecular formula R-C 9 H 11 N 2 O 4 S, where R is a variable side chain.

Moa of Penicillin

First antibiotic to have been manufacture in bulk All penicillin like antibiotics:  inhibit synthesis of peptidoglycan, essential part of the cell wall.

an  do not interfere with the synthesis of other intracellular components.

 do not affect human cells because human cells do not have cell walls.

Spectrum of Activity

used in the treatment of bacterial infections caused by susceptible, usually Gram-positive, organisms.

effective against many previously serious diseases such as syphillis and Staphylococcus infections .

Some members (e.g. amoxicillin) are also effective against Gram negative bacteria but not

Pseudomonas aeruginosa.

Moa of Penicillin

The β-lactam moiety (functional group) of penicillin binds to the DD-transpeptidase death due to osmotic pressure.

(links the peptidoglycan molecules in bacteria) → weakens the cell wall of the bacterium, causes cytolysis or In addition, the build-up of the bacteria's existing peptidoglycan.

peptidoglycan precursors triggers the activation of bacterial cell wall hydrolases and autolysins, which further digest Gram-positive bacteria are called protoplasts when they lose their cell wall. Gram-negative bacteria do not lose their cell wall completely and are called spheroplasts after treatment with penicillin.

Production of Penicillin

Penicillin was the first important commercial product produced by an aerobic, submerged fermentation and using a fed batch culture technique.

Used as input material for some semi synthetic antibiotics.

Secondary produced during metabolite, produced only in the stationary phase when growth of the fungus is inhibited by stress, not active growth.

PRODUCTION OF MONOSODIUM GLUTAMATE

Monosodium Glutamate (MSG)

MSG has first isolated as glutamic acid in 1866 by German chemist (Ritthausen) through the acidic hydrolysis of gliadin, a component of wheat gluten.

In 1908, Kikunae Ikeda, a Japanese chemist patented a process for isolating MSG from wheat flour and produced commercially under trade name “Ajinomoto” (the origin of flavour).

The Manufacturing Process

Preparation and Repulping Processess of Raw Materials  Natural crops is used as raw materials (easily obtained).

  Ex: Tapioca and sago or sugarcane (molasses).

Tapioca and sago powder are mixed with water to form starch slurry.

Liquefaction and Saccharification Process  Starch sluury is converted into glucose solution through enzymatic action.

Sterilization Process  The medium will sterilized using steam sterilization to eliminate contaminants.

The Manufacturing Process (cont)

Fermentation Process  The heat sterilized raw materials and other nutrients are put into fermenter.

 Microbes are added to convert glucose into glutamic acid.

Crystallization Process  Acidifying of fermentation materials are carried out to crystallized the glutamic acid produced.

 The glutamic acid crystal cake are separated from acidified fermentation broth.

Conversion of Glutamic acid to MSG  By adding glutamic acid cake into NaOH solution (food grade) to convert glutamic acid into MSG.

The Manufacturing Process (cont)

Cleaning of MSG  The impurities are removed by using active carbon to form more clean and clear MSG.

 Active carbon: many micro holes to attach impurities on its surface.

Crystallization of MSG   Clean MSG solution is concentrated by heating.

The crystal of MSG will be formed.

Drying of MSG  The crystal then are vibrated and transported through hot air in closed system until dry.

The Manufacturing Process (cont)

Sieving Process  Seggregating process to separate MSG crystall accordance to required size.

Packaging

MSG Production Process

Starch (Tapioca Flour, Maize Flour, Sago Flour) + H 2 O Starch slurry Liquefaction (85ºC cooled) Enzyme saccharification (60 hr, 55 60ºC) Glucose syrup and nutrient addition (ex Yeast Extract) Preculture of Brevibacterium lactofermentum cells Substrate sterilization (121 ºC)

Inoculation Batch Fermentation (1-2 weeks) Filtration (harvest) Ion Exchangers (to remove excess mineral salt) Acidification (pH 2.2 IEP) Cooling + Crystallization (40 days, 14 ºC) Glutamate acid slurry Separation Crude MSG (Magenta colour) Decolorization (Activated carbon, pH 6.4)

Filtration + NaOH Pure MSG (pH 6.9, 50% MSG) Final Filtration Crystallization Separation Sedimentation Drying Packing

INDUSTRIAL ALCOHOL FROM WASTES (OVERVIEW)

INDUSTRIAL ETHANOL

Industrial Production of Ethanol (Bio Oil Process)

Concentrated sugar cane molasses + mineral (Substrate preparation) Concentrated yeast stream (Pichina stipitis, S.cerevisiae, Candida schatae) Production fermenter (anaerobic) Batch Fermentation (7 days) Centrifugation/ Filtration Ethanol vapourizer Concentrated ethanol vapour Heat exchange Cooler Collection tank Bottling