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Bacteriology

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MYCOLOGY   STUDY OF FUNGI  
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PROTOZOOLOGY   STUDY OF PROTOZOA  
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PHYCOLOGY   STUDY OF ALGAE  
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LINNENS   DEVELOPED THE SYSTEM OF LATIN NOMENCLATURE  
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ROBERT HOOKE   DISCOVERED THE CELLS IN CORK/ COMPOUND MICROSCOPE IN MAGNIFYING SMALL OBJECTS  
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ANTON VAN LEEWENHOEK   BACTERIA IN CELLS/ ANIMALCULES PRESENT IN ENVIRONMENT  
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EDWARD JENNER   VACCINATION IMMUNIZATION  
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SEMMELWEIS   HAND WASHING (2 HOSPITAL TEACHING/NONTEACHING)  
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JOHN SNOW   EPIDIMIOLOGY OF CHOLERA (MAPPED LONDON WHERE THE WATER PUMP WAS REMOVED AND FOUND THAT IT WAS CONTAMINATED)  
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LOUIS PASTEUR   DISPROVE SPONTANEOUS GENERATION/HE WAS A CHEMIST THAT WAS HIRED TO FIND WHY THERE WAS MUCH SPOILAGE ON WINE / ALSO DEVELOPED VACCINE ON RABIES AND ANTHRAX  
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JOSEPH LISTER   FIRST SURGEON USING PHENOL COMPOUND  
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ROBERT KOCH   KOCH'S POSTULATE/FOUND WHAT CAUSE TUBERCOLOSIS  
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KOCH'S POSTULATE   1) THE SAME PATHOGEN MUST BE PRESENT IN EVERY CASE OF DISEASE  
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KOCH'S POSTULATE   2) PATHOGEN FROM THE DISEASED HOST MUST BE ISOLATED AND GROW IN A PURE CULTURE  
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KOCH'S POSTULATE   3) PATHOGEN FROM THE PURE CULTURE MUST CAUSED THE DISEASE WHEN IT IS INOCULATED INTO HEALTHY SUSCEPTIBLE LABORATORY ANIMAL  
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KOCH'S POSTULATE   4) PATHOGEN MUST ME ISOLATED FROM THE INOCCULATED ANIMAL AND MUST BE SHOWN TO THE ORIGINAL ORGANISM.  
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WAHR AND FANNY HESSE   DEVELOPED AGAR THAT ARE USED TO GROW PURE CULTURE / AGAR DOES NOT SOLIDIFIES EVEN IN HIGH TEMPERATURE  
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CHRISTIAN GRAM   DEVELOPED GRAM STAIN  
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DIMITRI IWANOWSKI   FILTERABLE VIRUSES(HE TOOK INFECTED TOBACO PLANTS AND FILTERED AND INFECT A HEALTHY PLANT)  
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PAUL ELRICH   CHEMOTHERAPHY FOR SYPHILLIS  
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ALEXANDER FLEMMING   ACCIDENTALLY DEVELOPED PENICILLIN  
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GERHARD DOMAGK   DISCOVERED PRONTONSIL (EFFECTIVE FOR TREATING STREPTOCOCCUS)  
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SULFA DRUGS   WAS DISCOVERED AFTER PENICILLIN BUT WAS FIRST MARKETED BEFORE PENICILLIN ON 1940  
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JAMES WATSON/FRANCIS CRICK/ ROSALING FRANKLIN/ MAURICE WILKINS   who discover the DNA STRUCTURE  
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SALKS/SABIN   who discover POLO VACCINE  
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CARL WOESSE   who discover THE THREE DOMAINS OF BACTERIA (ARCHEA/EUKARYA)  
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SURGEON GENERAL   CLOSES BOOKS ON INFECTIOUS DISEASE  
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CLINICAL APPEARANCE OF AIDS   EPIDIMIOLOGY 1980  
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WHO   ANNOUNCE ERRADICATION OF SMALLPOX  
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STANLEY PRUSINER   PRIONS (MAD COW DISEASE) RESPONSIBLE FOR ALL DIFFERENT NEURAL DISEASE  
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LUC MONTAGNIER & ROBERT GALLO   PURIFY AND CHARACTIRIZATION OF HIV ON 1983  
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POSITIVE IMPACT OF MICROBIOLOGY/BACTERIA/MICROORGANISM ETC   DEGREDATION OF WASTE-NITROGEN FIXATION-SEWAGE TREATMENT-BIOREMEDIATION- NORMAL FLORA (E COLI LIVING IN OUR INTESTINE, SKIN ETC.)  
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IMPACT OF MICROORGANISM   FOOD(BREADMAKING/FERMENTATION)BIOREMIDIATION-PROBIOTICS  
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IMPACT OF MICROORGANISM   MEDICAL PRODUCTS VACINE (INSULIN PRODUCED BY BACTERIA/INSECT PEST CONTROL/GENE THERAPY  
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BIOREMEDIATION   OIL SPILLS  
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NEGATIVE IMPACT   BUBONIC PLAGUE/INFECTED BLANKET (SMALLPOX)/REEMERGING OF DISEASE-ANTIBIOTIC RESISTANCE,BIOTERRORISM,IMMUNOSUPRESSION, LAX VACCINATION PROG.,  
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EMERGING DISEASE   HANTAVIRUS, LYME, AIDS, TOXIC SHOCK SYNDROME,WESTNILE, ESCHERICHIA ECOLI,EBOLA HEMMORHAGIC FEVER,  
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PANDEMIC   WORLDWIDE (AIDS)  
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ENDEMIC   SMALL DEFINE AREA  
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SYMBIOSIS   MUTUALISM/COMMENSALISM/PARASITISM  
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LIGHT MICROSCOPE   BRIGHTFIELD/DARKFIELD/FLUORESCENSE  
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ELECTRON MICROSCOPE   IMMAGE APPEAR ON SCREEN (TRANSMISSION/SCANNING)  
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COMPOUND MICROSCOPE   2 LENSE  
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BINOCULAR   2 EYEPIECE  
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OIL IMMERSION OIL (WHY?)   RISK OF HAVING LITTLE LIGHT/ USE REFRACTIVE INDEX TO KEEP LIGHT PATH INTO OBJECTIVE LENSE  
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DARKFIELD MICROSCOPE wHY?   FOR FRAGILITY/SIZE (USE FOR LIVING ORGANISM/FRAGILE/VERY SMALL ORGANISM)  
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FLUORESCENT MICROSCOPE   USE SPECIAL LIGHT UV/FLUORESCENT DYES  
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FLUOROCHROME   FLUORESCENT TAG  
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SCANNING MIC.   SCANNING OUTSIDE OBJECTS  
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TRANSMISSION MIC.   LOOKING THROUGH OBJECTS  
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TECHNIQUE   SMEAR/AIRDRY/FIXATION(HEAT)/STAIN  
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POSITIVE CHARGE   BASIC DYES -MOST CELL ARE NEGATIVE CHARGE  
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NEGATIVE CHARGE   ACIDIC DYES  
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DIFFERENTIAL STAIN   GRAM STAIN-BASIS-PROCESS  
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ACID FAST STAIN   BASIS(CELL WALL)-ACID FAST ORGANISM (MYOBACTERIA)- PROCESS  
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MYOBACTERIA   ACID FAST ORGANISM SPECIES- TUBERCOLOSIS  
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MYCOPLASM   DO NOT HAVE CELL ( NOT AN ACID FAST ORGANISM)  
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SAPHRONEN   COUNTER STAIN  
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CAPSULE STAIN   CARBOHYDRATE COAT AROUND CELL  
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ENDOSPERM STAIN   BACTERIA THAT HOLD TO WITHSTAND HARSH CONDITION (SURVIVAL)  
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FLAGELLA STAIN   ???/  
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MONOMORPHIC   1 SHAPE COCOUS/BACILLUS/SPIRAL  
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PLEOMORPHIC   VARIETY OF SHAPES  
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BACILLUS ANTHRACIS   GENUS/SPECIES (CAUSE ANTHRAX)  
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DIPLO BACILLUS   TWO ROD SHAPE  
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STREPTO BACILLUS   CHAIN OF ROD SHAPE  
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COCO BACILLI   ROUND SHAPE  
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VIBRIO   COMMA SHAPE  
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SPIRILLUM   WORM SHAPE  
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SPIROCHETE   SPIRAL SHAPE  
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FILAMENTOUS   FILAMENTS CLUSTER  
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DIPLOCOCCI   2 ROUND/CIRCLE SHAPE  
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STREPTOCOCCI   CIRCLE CHAIN  
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STAPHYLOCOCCI   CLUSTER OF CIRCLE  
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SARCINAE   PACKETS OF 8 CIRCLE  
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TETRAD   PACKETS OF 4 CIRCLE  
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GLYCOCALYX   SWEET COAT ON EXTERIOR CAPSULE-ALLOWS TO BE VERULENT (EASILY CAUSED DISEASE) (BIOFILM)  
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CAPSULE   MAKES ORGANISM MORE VERULENT BECAUSE OF NUTRIENTS (CARB), AND KEEPS MOISTURE THAT EASY TO ADHERE OR STICK  
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FILAMENTOUS PROTEIN APPENDAGES   FLAGELLUM/FLAGELLA -LOCOMOTION  
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MONOTRICHOUS   1 FLAGELLA  
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LOPTRICHOUS   MORE THAN 1 FLAGELLA  
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AMPITRICHOUS   1 OR MORE ON BOTH ENDS FLAGELLA  
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PERRITRICHOUS   FLAGELLA THAT SURROUNDS THE CELL  
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ATTACHMENT PILUS/PILLI   FIMBRIA/FIMBRIAE-ENVOLVE IN ATTACHMENT EX. NICERIA GNORRHEA(ADHESION)  
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CONJUGATION PILUS/PILLI   LONGER THAN FIMBRIA 1 BACTERIA CELL TRANSFER ITS DNA TO A DIFFERENT BACTERIA CELL  
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BACTERIA CELL WALL   ALMOST ALL BACTERIA HAVE CELL WALL EXCEPT FOR_______  
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PEPTIDOGLYCANS   PEPTIDES/GLYCAN(CARBOHYDRATES)ALTERNATE UNITS OF NAM/NAGATTACHED USING PEPTIDE CHAINS (AMINO ACIDS)  
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GRAM POSITIVE   -TECHOIC ACIDS ASSOCIATED WITH PEPTIDOGLYCANS(EXTRA REINFORCEMENT)-SEVERAL LAYERS OF PEPTIDOGLYCANS EXTERIOR-THICK-NO OUTER MEMBRANE-NO PERIPLASM-NO LIPOPOLYSACHARRIDES  
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GRAM NEGATIVE   -THIN PEPTIDOGLYCANS (THIN)-NO TECHOIC ACIDS-OUTER MEMBRANE-PERIPLASM CONTAINS PEPTIDOGLYCANS-LIPOPOLYSACHARRIDES (OUTERMEMBRANE) ORANGE-LIPID A ENDOTOXIN VERY IMPORTANT LAYER OF GRAM NEGATIVE  
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ARCHEA   PSEUDOPEPTIDOGLYCAN  
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PLASMA MEMBRANE   PHOSPOLIPID BILAYER  
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DIFFUSION   MOVING FROM MORE CONCENTRATION TO LESS CONCENTRATION  
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OSMOSIS   WATER MOVING FROM_____  
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TRANSPORT   FACILITATED/ACTIVE  
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FACILITATED TRANSPORT   -MOVEMENT WITH CONCENTRATION GRADIENT-NO ENERGY-PROTEIN AND DIFUSSION  
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ACTIVE TRANSPORT   MOVEMENT AGAINST CONCENTRATION GRADIENTENERGY REQUIREDPROTEIN AND ENERGY  
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CYTOPLASM   MEMBRANE WITH THINGS SUSPENDED IN IT CYTOSOL  
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RIBOSOME   2 CHEMICAL PARTSRIBOSOMAL RNAPROTEIN  
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RIBOSOME   2PHYSICAL PARTS30 S50 STHEN 70 S  
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INCLUSIONS   METOCHROMATIC GRANULESINCLUSION(BACTERIA CELLS WANTS TO TAKE MORE NUTRIENTS AND STORE IT) (IT IS ALSO USE FOR IDENTIFICATION)  
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ENDOSPORES IN BACTERIA   SURVIVAL NOT REPRODUCTIONALLOW THE BACTERIA TO WITHSTAND HARSH CONDITION  
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BACILLUS   CAN FORM ENDOSPORE(BACILLUS ANTHRACIS)  
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PROKARYOTE   SMALLERNO NUCLEUSNO MEMBRANESOME GLYCOCALYXCELL WALL EXCEPT FOR ________ AND ______PEPTIDOGLYCANPLASMA MEMBRANECYTOPLASMRIBOSOMES SMALLERCHROMOSOME SINGLEBINARY FUSSIONNO MITOSIS/ NO SEXUAL REPRODUCTION  
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EUKARYOTE   LARGERNUCLEUSGLYCOCALYX SOME NOT HUMANSNO PEPTIDOGLYCANSPLASMA MEMBRANECYTOPLASMRIBOSOME LARGERCHROMOSOMES MULTIPLE PAIRSMITOSIS/MEIOSISSEXUAL/ASEXUAL  
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FUNGI   EUKARYOTESNOT PLANT KINGDOMDONT CARRY ON PHOTOSYNTHESIS2 TYPES ( MOLD/YEAST)  
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MOLD   MULTICELLULAR  
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YEAST   UNICELLULAR  
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MYCOSES   DISEASE CAUSE BY FUNGI  
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STRUCTURE OF MOLDS   HYPHA(S)HYPAE(P)MYCELIUM(S)MYCELIA(P)SEPTAE  
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DIMORPHIC FUNGI   SOME FUNGI CAN BE YEAST OR MOLD AT DIFFERENT TEMPERATURE (YEAST-HI) (MOLD-LOW)  
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FUNGI NUTRIENTS INTAKE   HETEROTROPHSEXTRACELLULAR ENZYMES (BREAK DOWN FOOD)MYCELIA(EXTEND HYPHA TO GET FOOD)  
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SAPROBES/DECOMPOSERS   FUNGI IS DECOMPOSERS  
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FUNGI GROWTH REQ.   OXYGENTEMPERATURE CAN TOLERATE HIGH TEMP.PH CAN TOLERATE ACIDITYOSMOTIC PRESSURE WITHSTAND HIGH OP  
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FUNGI REPRODUCTION   EXIST AS HAPLOID BUT CAN ALSO BE DIPLOIDASEXUAL AND SEXUAL REP.SPORES-FOR REPRODUCTION NOT SURVIVALDIFF. MATING TYPES  
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HYPHAE FRAGMENTATION   BREAK APART HYPHA THEN BECOME NEW ORGANISM  
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YEAST   PRODUCE BY BUDDING  
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HETEROKARYON   FUNGI FUSE TO FORM CELL WITH 2 NUCLEI  
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DIPLOID ZYGOTE   FUNGI FORM 2 ZYGOTE  
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ASEXUAL REPRODUCTION IN FUNGI>? WHY?   GENETIC DIVERSITY  
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ZYGOMYCOTA   SEXUAL REPRODUCTION-HAS THE ABILITY TO FORM ZYGOSPHORE  
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ASCOMYCOTA   SEX REP.SEXUAL STRUCTURE THAT SUPPORTS SPORES AFTER SEX. REPR.  
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BASIDIOMYCOTA   SEX.REP.  
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IMPERFECT FUNGI   DO NOT CARRY ON SEXUAL REPRODUCTION ONLY CARRY ON ASEXUAL REPRODUCTION.  
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FUNGI NOT CLASSIFIED AS PLANT   NO CHLOROPHYL CELL WALL CONTAIN CARB. CALLED CHITINMULTICELLULARAUTOTROPHIC  
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