The document summarizes various physical and chemical methods used to control microorganisms. Physical methods include heat (through autoclaving, fractional sterilization, boiling), radiation (UV light, X-rays, gamma rays), and low temperatures. Chemical methods involve the use of disinfectants like phenol, alcohol, iodine, chlorine, heavy metals, dyes, detergents, aldehydes and ethylene oxide. Antibiotics work by inhibiting bacterial cell wall synthesis. Overall, the document outlines different sterilization techniques and their modes of action against microbes.
The document summarizes various physical and chemical methods used to control microorganisms. Physical methods include heat (through autoclaving, fractional sterilization, boiling), radiation (UV light, X-rays, gamma rays), and low temperatures. Chemical methods involve the use of disinfectants like phenol, alcohol, iodine, chlorine, heavy metals, dyes, detergents, aldehydes and ethylene oxide. Antibiotics work by inhibiting bacterial cell wall synthesis. Overall, the document outlines different sterilization techniques and their modes of action against microbes.
The document summarizes various physical and chemical methods used to control microorganisms. Physical methods include heat (through autoclaving, fractional sterilization, boiling), radiation (UV light, X-rays, gamma rays), and low temperatures. Chemical methods involve the use of disinfectants like phenol, alcohol, iodine, chlorine, heavy metals, dyes, detergents, aldehydes and ethylene oxide. Antibiotics work by inhibiting bacterial cell wall synthesis. Overall, the document outlines different sterilization techniques and their modes of action against microbes.
1. HIGH TEMPERATURE MOIST HEAT Coagulation of Cellular Autoclave(steam under Proteins pressue,121˚C at 15lbsq2)
2. FRACTIONAL Coagulation of Cellular Applied for heat sensitive
STERILIZATION Proteins materials, 100˚C for 3 successive days. A few seconds exposure. 3. BOILING Coagulation of Cellular Do not ensure sterilization, Proteins only destroy vegetative cells. Practice of exposing lab. Instruments provides disinfection. 4. PATEURIZATION Coagulation of Cellular Exposure at 62.8˚C for Proteins 30minutes, leads to killing of vegetative forms only. Spores and virus sustain this temperature. 5. DRY HEAT Oxidation of Cellular Proteins Applied for lab. Apparatus HOT AIR Exposure of 160˚C for 2 STERILIZATION hours. 6. INCINERATION Oxidation of Cellular Proteins Destruction by burning m.orgs. directly on flame. Used for hazardous stuff. 7. LOW TEMPERATURE Cessation of Metabolic Storage for longer periods Activities at temperature 4˚C-7˚C. Deep Freeze temperature -20˚C--70˚C. Liquid Nitrogen -196˚C is used to preserve cultures of viruses 8. DESSICATION Cessation of Metabolic Lyophilizer : Activities by drying(removal of Organisms are subjected to water)term used is extreme dehydration in Lyophilization: quick drying frozen state and then sealed in vacuum. Orgs. remain viable for years 9. OSMOTIC PRESSURE Distortion of cell via Applied for several food plasmolysis and plasmoptysis products: pickles, jams and jellies etc. 10. RADIATIONS Λ2650˚A, absorbed by Nucleic Less penetration power. ULTRAVIOLET LIGHT Acid where it forms Thymine Destructive microbes Dimers in which two adjacent present on the surface. Thymine forms a bond. Replication is inhibited. 11. X-RAYS High penetration power,ionization Production of mutants of DNA 12. GAMMA RAYS They create free hydrogen High penetration power. radicals, hydroxyl radicals and commercial sterilization of some peroxides which in turn packages of considerable causes different kinds of size. Sterilization of cellular damages. packaged food. 13. SURFACE Alteration in permeability Gas Liquid interface TENSION&INTERFACIAL characteristics of cytoplasmic Immiscible liquid interface TENSION membrane causing leakage of cellular substances resulting in cell damage. 14. FILTERATION Straining, variant size of pore Isolation of certain bacteria enable even separation of virus. and purification of Water,Air and any other desired product. CONTROL OF MICROORGANISMS BY CHEMICAL AGENTS
S.No. NAME MODE OF ACTION APPLICATION
1. PHENOL Disruption of cell, precipitation of Disinfection of surfaces. cellular proteins, inactivation of enzymes and leakage of amino acids from cell. 2. ALCOHOL Protein denaturants and lipid ETHYL ALCOHOL in solvents hence damage lipid conc. Of 50%-90% is complex in cell membrane, effective againt vegetative dehydrating agents may cause and non-sporing forms bacteriostatic conditions. 3. HALOGENS Irreversible oxidation and Disinfection of skin, water IODINE inactivation of metabolic and air. compounds(sulphydral Sterilization of food gp.a.a)may also cause utensils. halogenationof tyrosine residues of amino acids. 4. CHLORINE Antimicrobial activity comes Water Treatment, through HYPOCHLOROUS Food industry, ACID when free chlorine is Domestic and Medical Use. added in water, resultantis nascent oxygen, being strong oxidizing agent it aids in damage to cellular constituents. 5. HEAVY METALS & Combining with cellular proteins Silver, Gold and Copper, THEIR COMPOUNDS and inactivating them. In higher exhibits antimicrobial conc. Coagulate cytoplasmic activity, even in very less proteins, resulting in damage and concs. death to cell. 6. DYES UNCERTAIN, inhibitory effect Certain media is made TRIPHENYLMETHANE by interfering with cellular selective by incorporation DYES oxidation processes. of low conc. 7. ACRIDINE DYES Intercalate with DNA and inhibit Treatment of burns and Nucleic Acid synthesis. wounds and for ophthalmic application and bladder irrigation. 8. SYNTHETIC Surface Tension depressants. Detergent action. Cationic DETERGENTS Can be cationic or anionic. detergents are more germicidal then anionic compounds. 9. QUATERNARY Denaturation of protein, Used as disinfectants and AMMONIUM interference in glycolysis and sanitizers, preservative of COMPOUNDS membrane damage.(experimental ophthalmic. evidences suggests damages towards cell membrane) 10. ALDEHYDES Combines with nucleic acid and Sterilant. In gaseous form FORMALDEHYDE proteins. applied for sterilization of closed units. 11. GLUTERALDEHYDE Combines with nucleic acid and Broad spectrum of activity. proteins. Used as an sterilant for various lab. Equipment. 12. GASEOUS AGENTS Alkylation of cellular proteins. Effective sterilizing agent ETHYLENE OXIDE for heat and moisture sensitive materials. 13. β- PROPIOLACTONE Damage to cellular proteins. Effectively destructive for cells, but less penetration power and CARCINOGENICITY HAS LIMITED ITS PRACTCAL USE. CHEMOTHERPEUTIC AGENTS
S.NO ANTIBIOTICS MODE OF ACTION USES
1. INHIBITION TO CELL WALL Interference with final stages Effective towards Gram SYNTHESIS of PEPTIDOGLYCAN +ve bacteria PENECILLINS BIOSYNTHESIS. Inhibtion of Penecillium notatum transpeptidation reaction. 2. CEPHALOSPORINS Similar to that of penicillin. Less toxic, efficient for Cephalosporium acremonium Inhibit crosslinking of killing peptides. Bactericidal to growing cells. 3. CYCLOSERINE Inhibitory on peptidoglycan, Tuberculosis therapy. Streptomyces spp. peptide moiety. It inhibits both Due to side effects its Syntheticall prep. alanine racemase and D- utilization is limited. alanyl-D-alanine synthetase, which is involved in synthesis of side chain. 4. BACITRACIN Interference with regeneration Topical treatment of Bacillus subtilis of the monophosphate form of infections caused by bactopreno; from phosphate gram +ve. Being toxic form. not used for systemic infections. 5. VANCOMYCIN Inhibit peptidoglycan Effective for Gram +ve Streptomyces orientalis synthesis by binding D-alanyl- pathogens. D-alanine group 6. DAMAGE TO CELL Adversely affect permeability Polymyxins are MEMBRANE of cell. effective against Gram- POLYMYXINS ve bacteria. TYROCIDINES&GRAMICIDEINS Tyrocidines and Gramicidines are effective towards Gram +ve bacteria 7. POLYENE Acts on sterol containing cell Polyene, acts on fungi NYSTATIN membrane. and animal cell but not Streptomyces nourseii bacteria. AMPHOTERICIN STreptomycin nodusa 8. INHIBITION OF NUCLEIC Irreversibly binds with 30s Effective for Gram –ve ACID AND PROTEIN subunit mRNA. bacteria including SYNTHESIS Mycobacterium STREPTOMYCIN tuberculosis Streptomyces griseus TETRACYCLINE Interference with the binding Streptomyces species of aminoacyl-tRNA to 30s subunit ribosome, 9. ERYTHROMYCIN Inhibit protein synthesis by Effective for Gram +ve Streptomyces erthraeus combining 50s subunit, sides and –ve bacteria. associated with transpeptidation and translocation. 10. INHIBITION OF SPECIFIC Competitive inhibition Broad Spectrum ENZYME SYSTEM between an essential effective for various SULFONAMIDE metabolite PABA and a groups. metabolite analog a SULFONAMIDE 11. ANTIFUNGAL ANTIBIOTICS NYSTATIN Fungicidal, alter cell Restricted to fungi and Streptomyces nourseii membrane. yeast GRISEOFULVIN Treatment of some Penecillium griseofulvin Fungicidal, alter cell systemic mycoses membrane. 12. ANTIVIRAL AGENTS INTERFERON Interference in Protein Broadly work for ACYCLOGUANOSINE Synthesis various. AMANTADINE Nucleoside analogue Active against Herpes. Interfere with uncoating of Very effective towards virus and subsequent release Influenza A virus of nucleic acid