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A. Proteins
B. Peptones
C. *Amino acids
D. Lipids
E. Carbohydrates
A. meat
B. fish
C. meat and bone flour
D. casein
E. *all answers are correct
A. Brilliant green
B. Rivanol
C. Acriflavin
D. none of them.
E. *all of them
A. lipase
B. protease
C. hydrolase
D. *catalase
E. urease
A. lipase
B. protease
C. hydrolase
D. *catalase
E. urease
A. Oxydoreductases
B. Isomerases
C. Ligases
D. *Hydrolases
E. Transferases
A. Hydrolases
B. Isomerases
C. Transferases
D. Lyases
E. *Oxydoreductases
A. *Transferases
B. Ligases
C. Lyases
D. Oxydoreductases
E. Isomerases
A. age of bacteria
B. composition of nutrient medium
C. medium рН
D. *year season
E. temperatures, aeration
A. acid
B. alkali
C. gas
D. *acid and gas
E. fixing the finished products is not succeeded
A. Universal
B. Liquid
C. Selective
D. Elective
E. *Differential-diagnostic
A. mechanical
B. physical
C. chemical
D. biological
E. *all answers are correct
A. nucleic acids
B. *enzymes
C. metabolites
D. Plasmids
E. Transposons
A. Lipids
B. Proteins
C. *Polysaccharides
D. Carbohydrates
E. Amino acids
A. Polysaccharides
B. Lipids
C. *Proteins
D. Carbohydrates
E. Amino acids
A. adaptive
B. *endoenzymes
C. exoenzymes
D. constitutive
E. all answers are right
A. formation of singlet oxygen
B. formation of hydrogen peroxide
C. formation of ozone
D. *all answers are correct
E. all answers are incorrect
A. Virophage
B. *Bacteriophage
C. Arbovirus
D. Rhabdovirus
E. Provirus
A. the presence of the correct viral polymerase
B. *the presence of the correct virus receptor
C. the presence of a nucleus in the eucaryotic cell
D. the presence of cellular polyribosomes
E. the presence of the correct number of viral genome segments
A. Water - 50-60 %, dry weight - 40-60 %.
B. Water - 60-90 %, dry weight - 10-30 %.
C. *Water - 70-90 %, dry weight - 10-30 %.
D. Water - 40-50 %, dry weight - 50-60 %.
E. Water - 20-40 %, dry weight - 60-80 %.
A. synonym of term of «jar»
B. vehicle which allows to study chemical properties of bacteria
C. vehicle, in which it is possible to make sterilization of media
D. *vehicle which allows to make continuous cultivation of microorganisms in laboratory conditions
E. vehicle which allows to study antigenic properties of bacteria
A. the envelope
B. the polymerase
C. the icosahedral capsid
D. the lipid
E. *the nucleic acid
A. Skin
B. Meat
C. *Algae
D. Arthral cartilage
E. Bones
A. *initiation and regulation of virus replication
B. maintenance of the virus outside the cell
C. coding for the structural proteins of the virus
D. determining the group specific antigens of the virus
E. coding for the lipid components of the viral envelope
A. Mouse
B. Rat
C. Cat
D. Dog
E. *Chicken
A. does not have any effect according to the cell
B. affect RNA molecules
C. *affect DNA molecules and as a result forms thymine dimers
D. affect the ribosomes
E. affect the structure of cell wall
A. destroys cell DNA
B. destroys cell RNA
C. destroys cell mesosome
D. *forms a cavitation cavity, filled in the pair of liquid, with high pressure inside
E. an ultrasound does not influence on bacteria
A. *by a simple transversal division
B. by a mitosis
C. by spore formation
D. by sexual way
E. by a disjunctive way
A. Roux’s medium
B. Leffler’s medium
C. *Giss’s media
D. Ploskirev’s medium
E. EMB medium
A. Clostridium tetani, Clostridium perfringens
B. Mycobacterium tuberculosis, Vibrio cholerae
C. Corynebacterium diphtheriae, Salmonella typhi
D. *Brucella abortus
E. Lactobacillus acidophilus
A. Clostridium tetani, Clostridium perfringens
B. Mycobacterium tuberculosis, Vibrio cholerae
C. *Corynebacterium diphtheriae, Salmonella typhi
D. Brucella abortus
E. Lactobacillus acidophilus
A. Staphylococcus aureus
B. Shigella flexneri
C. Salmonella patience
D. *Yersinia pestis
E. Streptococcus pyogenes
A. Obligate anaerobes
B. Capneic bacteria
C. *Obligate aerobes
D. Microaerophilic bacteria
E. Facultative anaerobes
A. %.
B. %.
C. *55 %.
D. %.
E. %
A. Stationary
B. *Exponential
C. Initial
D. Death
E. Expotential
A. Initial
B. Exponential
C. *Accumulations
D. Stationary
E. Decline
A. Agglutination test
B. Complement fixation test
C. *Precipitation test
D. Gruber’s test
E. Indirect hemagglutination test
A. appearance of areas of darkening on a mat red background
B. the changes of medium color
C. appearance of bright red colonies of microbes, if they cause haemolysis
D. *appearance of colorless areas surround the colonies on mat red background if the have hemolytic activity
E. appearance of colorless colonies
A. Making meat small
B. Filtration
C. *Extraction
D. Boiling
E. Sterilization
A. % sodium sulfate
B. % acids
C. *1 % alkali
D. % iron sulfate
E. % sodium chloride
A. proteins
B. lipids
C. *agar-agar
D. carbohydrates
E. there is no correct answer
A. *Joint cultivation of anaerobic bacteria and Serratia marcescens, which utilizes an oxygen intensively
B. Cultivation of anaerobes in the organism of laboratory animals
C. Cultivation of anaerobes in the chicken embryos
D. All answers are correct
E. All answers are wrong
A. use of Gas generating box
B. application of pyrogallol on the bottom of the jar
C. use the high column of nutrient medium
D. introduction of pieces of liver or muscles and vitamin K3 as supplement in the medium
E. *right answer A, B, D
A. use of Gas generating box
B. to cover the surface of medium with the layer of vaseline oil
C. use the high column of nutrient medium
D. *right answers B and C.
E. right answers A, B and C
A. use of Gas generating box
B. to cover the surface of medium with the layer of vaseline oil
C. use the high column of nutrient medium
D. *regeneration of nutrient medium before inoculation
E. correct answer is not present
A. formation of flakes, fastened to the inner wall of test tube
B. by diffuse turbidity
C. formation of grains, fastened on the inner wall of test tube.
D. formation of pellicle on the surface of medium
E. *correct answers A and C
A. Crumble-like
B. homogeneous
C. viscid
D. mucous
E. *all answers are correct
A. Lactic-acid fermentation
B. alcoholic fermentation
C. butiric-acid fermentation
D. *all answers are correct
E. all answers are wrong
A. pantothenic acid
B. Cholin
C. nicotine acid
D. *all answers are correct
E. all answers of incorrect
A. Polio
B. Hepatitis
C. *Tobacco mosaic virus
D. Potato blight
E. Influenza
A. the acute titer is less than 10
B. the convalescent titcr is greater than 20
C. there is a twofold rise in titer
D. *there is a fourfold rise in titer
E. there is no change in titer
A. on DNA of cell
B. on мРNA
C. on a cytoplasm membrane
D. on a cellular wall
E. *on DNA, located in the place of connection of mesosome and cytoplasm membrane
A. Contain DNA
B. Contain RNA
C. Are extracellular
D. Reproduce independently
E. *Induce host metabolism
A. *Herpes
B. Rhinovirus
C. Influenza
D. Rabies Virus
E. echovirus
A. protein
B. enzymes
C. nucleic acid
D. *a capsid
E. an envelope
A. *WI-38.
B. HeLa.
C. HEp-2.
D. KB.
E. Detroid 5
A. HeLa.
B. HEp-2.
C. KB.
D. Detroit 5
E. *All of the above
A. Phage structural proteins
B. Proteins that help with phage assembly without becoming part of the virion structure
C. Proteins involved in cell lysis and phage release
D. *All of the above
E. None of the above
A. poxvirus
B. retrovirus
C. *picornavirus
D. herpesvirus
E. adenovirus
F.
A. *capsomers
B. capsid
C. nucleocapsid
D. virion
E. envelope
A. *Phage structural proteins
B. DNA polymerase
C. Early proteins
D. All of the above
E. None of the above
A. Temperate virus
B. Naked virus
C. Virion
D. *RNA phage
E. DNA phage
A. Poxviruses
B. Paramyxoviruses
C. Picornaviruses
D. *Parvoviridae
E. Orthomyxoviruses
A. herpes virus
B. mumps
C. influenza
D. chicken pox
E. *picorna virus
A. I. Mechnikov
B. S. Vinogradsky
C. *L. Pasteur
D. R. Koch
E. E. Ru
A. staphylococci and streptococci
B. escherichia and salmonellas
C. mycobacteria and bordetella
D. *rickettsia and chlamidia
E. vibrios and treponema
A. consistencies
B. density
C. color
D. *all answers are correct
E. all answers are wrong
A. metabolic
B. *amphibolic
C. associative
D. dissociative
E. polybolic
A. fermentation
B. respiration
C. photosynthesis
D. *all answers are correct
E. all answers are wrong
A. gram-positive
B. gram-negative
C. form capsules
D. *form spores
E. form pili
A. carbon acid and water
B. glucose and lactose
C. carbon acid and nitrogen
D. mannitol and methanol
E. *indole and hydrogen sulphide
A. hours
B. hours
C. hours
D. *48 hours
E. hour
A. *The changes of the color from a pinky to yellow of the column of agar
B. The changes of the color from a pinky to yellow the slant surface of agar
C. The changes of the color from a pinky to red the slant surface of agar
D. The changes of the color from a pinky to yellow of the column of agar and the slant surface of agar
E. The changes of the color from a pinky to red of the column of agar
A. Yolk-salt agar
B. Buchin’s medium
C. Mannitol-salt agar
D. Blood-sugar agar
E. *Right answers A and C
A. Zeissler’s method
B. Shukevich’s method
C. Veynberg’s method
D. *Fortner’s method
E. Pasteur’s method
A. -90 °С during 10 min
B. -80 °С during 30 min
C. -60 °С during 30 min
D. -100 °С during 30 min
E. *80-90 °С during 1 hour.
A. sterilization by water bath at 58-60 °С during a hour 2-3 days one after the other
B. single sterilization by water bath at 98-100 °С during 10 min
C. sterilization by water bath at 58-60 °С during a hour 3-4 days one after the other
D. *sterilization by water bath at 58-60 °С during a hour 5-6 day one after the other
E. sterilization by water bath at 80-90 °С during a hour 2-3 days one after the other
A. Mueller’s medium
B. % alkaline peptone water
C. Ru’s medium
D. Blood agar
E. *Saburo’s medium
A. *Mueller’s medium
B. % alkaline peptone water
C. Ru’s medium
D. Blood agar
E. Saburo’s medium
A. heterotrophs
B. autotrophs
C. lithotrophs
D. organotrophs
E. *chemotrophs
A. Mueller’s medium
B. % alkaline peptone water
C. Ru’s medium
D. *Agar with furazolidonum and tween
E. Saburo’s medium
A. deleting bacterial and fungal spores of the objects of environment
B. elimination of pathogenic microorganisms in a wound
C. *decontamination of pathogenic microorganisms is the
D. diminishing the degree of microbial contamination of skin and mucous membranes
E. elimination viruses in the environment
A. Precipitating serum
B. *Agglutinating serum
C. Neutralizing serum
D. Hemolytic serum
E. Right answer is not present
A. acid
B. alkali
C. gas
D. *acid and gas
E. fixing the finished products is not succeeded
A. Andrede
B. Neutral red
C. *Phenol red
D. Bromthymol blue
E. Thymol blue
A. Flat
B. Convex
C. Dome-shaped
D. Pitted
E. *All answers are correct
A. Biochemical and serologic
B. *Cultural (signs of growth) and morphological
C. Tinctorial and biochemical
D. Susceptibility to phages and antibiotics
E. Right answer is not present
A. *134 °С 40 minutes
B. °С 20 minutes
C. °С 15 minutes
D. °С 10 minutes
E. °С 30 minutes
A. *does not have capsules
B. have capsules
C. sometimes does not have flagella
D. low or absent virulence
E. easily phagocytable
A. *easily phagocytable
B. poorly phagocytable
C. biochemically more active
D. isolated in the acute stage of disease
E. have capsules
A. *enzymes
B. toxins
C. allergens
D. plasmids
E. antigens
A. allergic tests
B. *inoculation of laboratory animals
C. agglutination test
D. biochemical reactions
E. cultivation on species
A. *Gononococci
B. Vibrio cholerae
C. Shigella
D. Corynebacterium diphtheriae
E. Salmonella typhi
A. Roux’s method
B. Gram’s method
C. Inoculation by a needle
D. *Drigalsky’s method
E. Morozov’s method
A. *character of growth
B. character of staining
C. enzyme activity
D. all answers are correct
E. all answers are wrong
A. character of bacterial staining
B. *character of growth of bacteria on/in nutrient medium
C. character of biological features of bacteria
D. all answers are correct
E. all answers are wrong
A. Carbonic acids and waters
B. Glucose and lactose
C. Carbonic acid and nitrogen
D. Mannitol and methanol
E. *Indole and hydrogen sulfide
A. *Kitt-Tarozzi’s medium
B. Giss’s medium
C. Zeissler’s medium
D. Endo’s medium
E. Ploskirev’s medium
A. equipment for anesthesia
B. *nutrient media
C. prostheses
D. endoscope instruments
E. catgut
A. formaldehyde
B. chloroform
C. beta-propiolactone
D. ethylene oxide
E. *methane
A. Tuberculosis
B. Botulism
C. Tetanus
D. Salmonellosis
E. *All answers are correct
A. Veinberg’s medium
B. Zeissler’s medium
C. *Giss’ media
D. Kitt-Tarozzi’s medium
E. Milk
A. Bacteriological loop
B. *Spatula
C. Bacteriological needle
D. Jar
E. All answers are correct
A. *Bacteriological loop
B. Spatula
C. Bacteriological needle
D. All answers are wrong
E. All answers are correct
A. Pasteur’s serial dilution
B. Koch’s method
C. Drigalsky’s method
D. Streak’s method
E. *Leffler’s method
A. *on solid nutrient media
B. in liquid nutrient media
C. in laboratory animals
D. in chicken embryo
E. in cell cultures
A. Fortner’s method
B. *Drigalsky’s method
C. Membrane filters’ method
D. Gins’s method
E. Leffler’s method
A. For cognition
B. For treatment
C. *For diagnostic
D. For prophylactic
E. For anamnesis
A. allergic tests
B. biotests in animals
C. *polymerase chain reaction
D. phage typing
E. examination of bacterial susceptibility to antibiotics
A. tubes
B. Petry’s plates
C. *rubber corks
D. metallic instruments
E. heat-resistant powders
A. By keeping in incubator at 37 °С for a few hours.
B. By keeping in incubator at a temperature 42 °С for a few hours
C. By keeping at 18-20 °С. For a few hours
D. *By keeping in incubator for a few days at 37 °С.
E. Right answer is not present
A. To cool the tested material before inoculation, as spores are insusceptible to the action of low temperatures
B. *To heat the tested material before inoculation, as spores are heat stable
C. To inoculate tested material and cultivate it in anaerobic conditions
D. To inoculate tested material, which contains spore forming bacilli in laboratory animals
E. To separate microorganisms according to their spore formation is impossible
A. To inoculate tested material on the upper part of slant agar
B. *To inoculate tested material in the drop of fluid in the lower part of slant agar
C. To do inoculation of tested material by a prick in the slant agar
D. To separate microorganisms is impossible
E. To add to the tested material some substance which cause coagulation flagella protein
A. *By wet-mount technique
B. By Grey’s technique
C. Staining according to Zdrodovsky’s technique
D. By scanning microscope
E. By radioisotope method
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