Explore topic-wise InterviewSolutions in .

This section includes InterviewSolutions, each offering curated multiple-choice questions to sharpen your knowledge and support exam preparation. Choose a topic below to get started.

1.

What is the name of the method used to attach enzymes to stationary solids by weak physical forces?(a) Absorption(b) Cross linking(c) Adsorption(d) Capillary actionThis question was posed to me in exam.Origin of the question is Methods of Immobilization topic in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct option is (c) Adsorption

The best I can EXPLAIN: ATTACHMENT of enzymes to stationary SOLIDS by weak physical forces such as VANDER WAALS forces or dispersion forces. Active site is normally unaffected and nearly full activity is observed. Desorption of enzymes is a common problem.

2.

Which of the following are natural mineral polymers?(a) Cellulose(b) Dextran(c) Agar(d) SilicaThe question was posed to me in an internship interview.My query is from Methods of Immobilization topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The CORRECT choice is (d) Silica

The explanation is: NATURAL polymers are which will be polysaccharides are cellulose, dextran. Agar, agarose, chitin, alginate. Natural polymers of protein categories are collage, albumin. INORGANIC natural polymers are bentonite and silica. Inorganic PROCESSES materials are GLASS, metals, etc.

3.

Which of the physical property of the matrices particularly determine the surface area and binding capacity?(a) Swelling behaviour(b) Mechanical strength(c) Compression behaviour(d) Pore parametersI have been asked this question in final exam.My query is from Methods of Immobilization in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right choice is (d) Pore parameters

For explanation I would say: Physical characteristics of the MATRICES such as MEAN particle diameter, swelling behaviour, MECHANICAL strength and COMPRESSION behaviour, etc. These physical characteristics are important for the performance of the immobilized conditions. Pore parameters and particle size determine the total surface area.

4.

In physical adsorption the enzymes are attached to the matrix through hydrogen bonding, van der Waals forces, or hydrophobic interactions; whereas in ionic bonding, the enzymes are bound through?(a) Hydrophilic linkage(b) Di-sulphide bonding(c) Salt linkages(d) Cross-linkingThe question was posed to me in an online quiz.Enquiry is from Methods of Immobilization topic in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right option is (c) Salt linkages

For explanation: The simplest immobilization method is nonspecific adsorption, based on physical adsorption or IONIC bonding for the drug MOLECULES with the polymeric molecules.The bonding between the drug and the polymer COMPOUND is REVERSIBLE. It also influences the strength of the INTERACTION.

5.

What is the method name that is based on the occlusion of an enzyme within a polymeric network that allows the substrate and products to pass through but retains the enzyme?(a) The entrapment method(b) Covalent coupling(c) Microencapsulation(d) Hollow fibreThis question was addressed to me in examination.This intriguing question comes from Methods of Immobilization topic in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct OPTION is (a) The entrapment method

To ELABORATE: In this method, the enzyme is not bound to the matrix or MEMBRANE. There are different approaches to entrapping ENZYMES such as gel or fibre entrapping and micro-encapsulation.

6.

The most common procedures of irreversible enzyme immobilization are covalent coupling, entrapment or micro-encapsulation and ____________(a) Hydrophilic linkage(b) Di-sulphide bonding(c) Covalent bonding(d) Cross-linkingI got this question in an internship interview.Enquiry is from Methods of Immobilization topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right answer is (d) Cross-linking

To explain: The concept of IRREVERSIBLE immobilization MEANS that once the biocatalyst is ATTACHED to the support it cannot be detached without destroying either the biological activity of the enzyme or the support. Thus the most COMMON procedures of irreversible enzyme immobilization are covalent coupling, entrapment or micro-encapsulation and crosslinking of the enzyme with POLYMERS.

7.

Who reported the first industrial use of immobilized enzymes in 1967?(a) Robert Hook(b) Chibata and co-workers(c) James Watson(d) Kary MullisI had been asked this question in an internship interview.My question is from Methods of Immobilization topic in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct option is (b) CHIBATA and co-workers

To elaborate: They have ALSO developed the immobilization of ASPERGILLUS oryzae aminoacylase for the resolution of synthetic racemic D-L amino acids. In their work fungal aminoacylase was immobilised on DEAE-Sephadex through IONIC bonding. They used this system to produce l-aspartate from ammonium fumarate.

8.

What term is given to “enzymes physically confined or localized in a certain defined region of space with retention of their catalytic activities, and which can be used repeatedly and continuous?(a) Localized enzymes(b) Localisation of enzymes(c) Immobilized enzymes(d) Catalysed enzymesI have been asked this question during an online exam.I want to ask this question from Methods of Immobilization topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»
9.

What is the name of the method used to cross link enzyme molecules with each other using agents such as glutaraldehyde?(a) Cross linking(b) Polyacrylamide(c) Agar(d) PolyacrylateThis question was posed to me at a job interview.My enquiry is from Methods of Immobilization in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct CHOICE is (a) Cross linking

To elaborate: Cross-linking is to cross link ENZYME molecules with each other USING AGENTS such as glutaraldehyde. Features are similar to covalent bonding. Several methods of crosslinking are COMBINED.

10.

Which membrane configuration is used for separating enzyme from substrate and product solution?(a) Packed column reactor(b) Hollow fibre configuration(c) Fluidized bed reactor(d) Stirred tank reactorThis question was addressed to me in my homework.This key question is from Methods of Immobilization in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct option is (b) HOLLOW fibre configuration

Explanation: Hollow fibre configuration is a very popular arrangement for separating enzyme from SUBSTRATE and product can be taken out easily. Hollow fibres CONTAINING a stationery enzyme SOLUTION. Mobile fluid OUTSIDE fibres containing substrate and products.

11.

Membrane materials include: Nylon, cellulose, polysulfone and _______________(a) Collagen(b) Polyacrylamide(c) Agar(d) PolyacrylateThe question was asked by my college professor while I was bunking the class.My doubt is from Methods of Immobilization topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer» RIGHT answer is (d) Polyacrylate

Best explanation: Membrane materials are the materials by which the membrane will be constructed. The enzyme solution may be CONFINES between thin semi permeable membranes. Membrane materials include NYLON, CELLULOSE, polysulfone, polyacrylate.
12.

Which one is a matrix for entrapment?(a) Cellulose(b) Polysulfone(c) Nylon(d) CollagenThis question was posed to me in exam.I'd like to ask this question from Methods of Immobilization topic in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right CHOICE is (d) COLLAGEN

For explanation I would say: The matrices for ENTRAPMENT are Ca- alginate, AGAR, polyacrylamide, collagen. Membrane materials are enzyme solutions which will be confined between THIN semipermeable membranes. Membrane materials include nylon, cellulose, polysulfone, polyacrylate.

13.

Why is the enzyme solution mixed with a polymeric fluid?(a) To make it more potent(b) Faster reaction(c) More active sites on the surface(d) Solidifies into various formsThis question was addressed to me in an internship interview.My question is from Methods of Immobilization in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The CORRECT answer is (d) Solidifies into various forms

To explain: The ENZYME SOLUTIONS are mixed with a polymeric FLUID which will solidify the enzymes into various forms. The solidification depends on application. The polymeric material is semi-permeable. Large is the molecular weight enzymes cannot diffuse out, small SUBSTRATE and product molecules can.

14.

Catalyst reuse is an advantage of immobilized enzyme systems.(a) True(b) FalseThis question was posed to me in an internship interview.This intriguing question comes from Methods of Immobilization topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right option is (a) True

The explanation: The enzymes which were immobilized can be reused. Since the enzymes f=don’t GET wash off fully, and the active sites are preserved by staking the enzymes all together in a polyester gel. This has advantages of easier OPERATION, easier PRODUCT separation, and wider CHOICE of reactors.

15.

Which enzyme gives Acrylamide as a product?(a) Nitrile Hydratase(b) Glucose isomerase(c) Penicillin acylase(d) Beta-GalactosidaseThis question was addressed to me in exam.This intriguing question comes from Methods of Immobilization in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right CHOICE is (a) Nitrile Hydratase

The best EXPLANATION: Acrlamide is a monomer which is used for production of a lot of substances. It is produced by the addition of WATER to ACRYLAMIDE. The catalyst used in this process is nitrile hydratase. This catalyst is difficult to regenerate. Thus we have to use immobilised nitrile hydrates.

16.

What is the product obtained from glucose isomerase?(a) Amino acids(b) High fructose corn syrup(c) Penicillin(d) AcrylamideThis question was addressed to me in exam.This key question is from Methods of Immobilization topic in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct option is (B) High fructose corn syrup

To explain I WOULD SAY: In corn syrup production the starch is broken down by enzymes. To make, high fructose corn syrup, the corn syrup has to be further broken down or processed by GLUCOSE isomerase. This step helps to CONVERT some of the glucose into fructose.

17.

What is the term given to restriction of enzyme mobility in a fixed space?(a) Enzyme deactivation(b) Enzyme saturation(c) Enzyme activation(d) Enzyme immobilizationThis question was addressed to me in quiz.I'd like to ask this question from Methods of Immobilization in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct choice is (d) Enzyme immobilization

Explanation: Immobilized enzymes refers to enzymes being physically CONFINED to or has been localised in a defined region of space. This ALSO helps them to retain their CATALYTIC activities which can be used continuously. The containment of enzyme solution WITHIN a confined space for the PURPOSE of retaining and re-using enzyme in processing equipment.

18.

The rate of enzyme conversion of the substrate will decrease with temperature.(a) True(b) FalseThis question was posed to me during an online interview.I want to ask this question from Methods of Immobilization topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct ANSWER is (b) False

Best explanation: It will increase. The RATE of enzyme conversion of the substrate will increase with temperature up to an optimum.Above this temperature, enzyme activity will decrease as enzyme denatures. THERMAL denaturation of the enzyme can occur after a certain point of INCREASED temperature.

19.

If the substrate contains ionic groups, what happens to the pH of the medium?(a) The pH of medium increases(b) The pH of medium decreases(c) The pH of medium remains same(d) The pH of medium affects the affinity of substrate to enzymeI have been asked this question at a job interview.The question is from Methods of Immobilization in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right option is (d) The pH of medium AFFECTS the affinity of substrate to enzyme

Easy explanation: Some CASES, the substrate may contain ionic groups, and the pH of medium affects the affinity of substrate to enzyme. This may lead to major changes in the binding of the enzyme to the substrate. This may damage some VITAL REACTIONS in our body.

20.

Variation in pH of medium result in changes of ionic form of the active site.(a) True(b) FalseThis question was posed to me in class test.My doubt is from Methods of Immobilization topic in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct answer is (a) True

Easy explanation: Variation in pH of MEDIUM result in changes of IONIC form of the active site and activity of enzyme, hence the reaction rate. Variation in pH of medium can also result in changes of the maximum reaction rate, Km stability of the enzyme. Enzyme are active only over small RANGE of pH due to the active site functional group charges (ionic form) and the three dimensional SHAPE of enzyme are pH-dependent.

21.

What is the suitable form of ionic group of enzymes?(a) Acidic or basic(b) Acidic(c) Basic(d) neutralThis question was posed to me in exam.I'd like to ask this question from Methods of Immobilization in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct option is (a) Acidic or basic

The explanation: Certain enzyme have ionic group on their active sites, and these ionic group must be in a suitable FORM (acid or base) to function. Variation in PH of medium result in changes of ionic form of the active site, activity of enzyme, hence the reaction rate, AFFECT the maximum reaction rate, Km STABILITY of the enzyme.

22.

Why are Enzymes active only over small range of pH?(a) Its enzymes property(b) Due to non-active site functional group charges(c) Due to the active site functional group charges(d) It prevents from structure destructionThe question was posed to me during an online interview.Question is taken from Methods of Immobilization topic in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right answer is (c) Due to the active site FUNCTIONAL GROUP charges

The best I can explain: Enzyme are active only over small range of PH due to the active site functional group charges (ionic FORM) and the three dimensional shape of enzyme are pH-dependent. Certain enzyme have ionic group on their active sites, and these ionic group must be in a suitable form (acid or BASE) to function.

23.

pH range required for streptomycin production is __________(a) 7-8(b) 5-8(c) 4-5(d) 9-10The question was asked in an online interview.My question comes from Production of Antibiotics (Isolation of Fermentation Products) in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right ANSWER is (a) 7-8

To EXPLAIN: The OPTIMUM temperature for fermentation should be in the range of 25 to 30°C. The optimum PH range should be in the range of 7.0 and 8.0. High RATE of streptomycin production occurs in the pH range of 7.6 to 8.0.

24.

How is streptomycin recovered?(a) Paper chromatography(b) Hydrophobic chromatography(c) Size exclusion chromatography(d) Ion exchange chromatographyThe question was posed to me by my college director while I was bunking the class.Origin of the question is Production of Antibiotics (Isolation of Fermentation Products) in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer» RIGHT choice is (d) Ion exchange chromatography

The best explanation: STREPTOMYCIN is an antibiotic which is used to TREAT a number of bacterial infections. It is an extracellular product so they are removed by adsorption to ion exchange columns in chromatography. The period of operation is short and streptomycin sulfate is obtained in a single fraction with an OVERALL yield of approximately 60 percent at a purity of 400 to 600 UNITS per mg.
25.

Streptomycin is _____ antibiotic.(a) Narrow spectrum(b) Broad spectrum(c) Narrow and broad spectrum(d) Medium spectrumThis question was posed to me in semester exam.Enquiry is from Production of Antibiotics (Isolation of Fermentation Products) in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right OPTION is (b) BROAD spectrum

For EXPLANATION: STREPTOMYCIN has amino cyclohexanol moiety. It is effective against gram –ve organisms but yet it is broad-spectrum antibiotic. It is used for the treatment of TUBERCULOSIS. Its side effect is nephrotoxicity.

26.

How is penicillin stored?(a) Filtration(b) Crystallization(c) Distillation(d) SublimationThis question was posed to me in exam.This question is from Production of Antibiotics (Isolation of Fermentation Products) topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct choice is (b) Crystallization

For explanation: Pure metal salts of penicillin can be SAFELY sterilized by dry heat if DESIRED. Thereafter, the aqueous solution of penicillin is subjected to crystallization. The alkali metal salts of penicillin are extremely soluble in WATER, and methods THEREFORE known for crystallizing them have employed organic solvents under nearly anhydrous CONDITIONS.

27.

What is the precursor of penicillin?(a) Benzylpenicillin(b) Isopenicillin N(c) phenylacetic acid(d) L-α aminoadipic acidThis question was addressed to me in examination.Query is from Production of Antibiotics (Isolation of Fermentation Products) topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct option is (c) phenylacetic acid

Easiest explanation: Benzylpenicillin (Penicillin G) is a narrow spectrum antibiotic used to treat infections caused by some bacteria. It is a NATURAL penicillin antibiotic administered intravenously or intramuscularly. Penicillin G MAY ALSO be used in CASES such as prophylaxis against susceptible organisms.

28.

The doubling time of Penicillium notatum is ___________(a) 6 hrs(b) 5 hrs(c) 4 hrs(d) 3 hrsI got this question in final exam.This intriguing question originated from Production of Antibiotics (Isolation of Fermentation Products) in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The CORRECT OPTION is (a) 6 hrs

Explanation: Growth PHASE is of 40 hrs duration with a doubling time of 6 hrs. Oxygen supply becomes CRITICAL during this phase due to an increase in viscosity of the medium. Production phase duration is 120 to 180 hrs.

29.

pH required for the production of penicillin will be ______________(a) 8.0(b) 7.5(c) 6.5(d) 5.0This question was posed to me in a job interview.Enquiry is from Production of Antibiotics (Isolation of Fermentation Products) in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The CORRECT option is (C) 6.5

Explanation: The pH should be has to be between 6.4 and 6.8 during the active production phase of penicillin. All the necessary precursors, ammonia, sugar, carbon dioxide, oxygen is controlled, by THOROUGH monitoring of TEMPERATURE and pH for OPTIMAL antibiotic production.

30.

Penicillium chrysogenum produce penicillin.(a) True(b) FalseThis question was addressed to me by my college director while I was bunking the class.The doubt is from Production of Antibiotics (Isolation of Fermentation Products) in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer» CORRECT answer is (a) True

Best explanation: Penicillium chrysogenum or P. Notatum (formerly) is a SPECIES of fungus. COMMON in temperate and subtropical regions. It has rarely CAUSED human disease. It is the source of SEVERAL β-lactam antibiotics, most significantly penicillin. Other secondary metabolites include roquefortine C, Meleagris, etc.
31.

Penicillin inhibits cell wall synthesis.(a) True(b) FalseThe question was asked in a job interview.My question is from Production of Antibiotics (Isolation of Fermentation Products) topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»
32.

Penicillin is active against ____________(a) Gram +ve bacteria(b) Gram-ve bacteria(c) All virus(d) All bacteriaI have been asked this question in class test.The origin of the question is Production of Antibiotics (Isolation of Fermentation Products) in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right ANSWER is (a) GRAM +ve bacteria

Explanation: First discovered by Alexander Fleming in 1929. Natural penicillin is active against a variety of gram +ve bacteria ORGANISMS. They are labile in acids and become inactive when its beta-lactam ring is cleaved by beta-lactamase ENZYME.

33.

How inoculum is prepared in the production of antibiotics?(a) On solid media(b) On liquid media(c) First on solid media than on liquid media(d) On suspensionThis question was addressed to me in exam.Enquiry is from Production of Antibiotics (Isolation of Fermentation Products) topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct option is (C) First on solid media than on liquid media

To ELABORATE: Inoculum development BEGINS on solid media, and then liquid media are used; the media used are specific for inoculum development. Spore SUSPENSION is prepared for inoculum. This will be then transferred to the fermenter.

34.

Antibiotics are mainly produced by _________(a) Bacteria(b) Algae(c) Fungi(d) Fungi and bacteriaThis question was addressed to me in examination.The above asked question is from Production of Antibiotics (Isolation of Fermentation Products) topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»
35.

How many antibiotics have still been isolated?(a) 5000(b) 2000(c) 7000(d) 3000This question was posed to me during a job interview.My doubt stems from Production of Antibiotics (Isolation of Fermentation Products) topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer» RIGHT answer is (c) 7000

To explain: Although more than 7,000 ANTIBIOTIC compounds have been isolated till date, only 100 or so are being used to treat human, animal and plant diseases. The first antibiotic DISCOVERED was penicillin by Alexender FLEMING.
36.

Who discovered the first antibiotic?(a) Alexander Fleming(b) Louis Pasteur(c) Francis Crick(d) Kary MullisThe question was posed to me in an interview for internship.The doubt is from Production of Antibiotics (Isolation of Fermentation Products) topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct option is (a) ALEXANDER Fleming

For explanation I would say: The antibiotic penicillin was discovered by Alexander Fleming in 1929, but its commercial production commenced only during the early 1940s. Fleming was ALSO the first to raise a concern about the potential of bacteria developing resistance due to the EXPLOITATION of ANTIBIOTICS, a problem which poses a MAJOR threat to healthcare in this era.

37.

What are antibiotics?(a) Nutrient supplements(b) Anti-cancer drugs(c) Anti-microbial drugs(d) Anti-ulcer drugsThe question was asked in unit test.My question comes from Production of Antibiotics (Isolation of Fermentation Products) topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»
38.

In a chemostat operating under steady state, a bacterial culture can be grown at dilution rate higher than the maximum growth rate by _________(a) Partial cell recycling(b) Using sub optimal temperature(c) pH cycling(d) Substrate feed rate cyclingI have been asked this question by my college professor while I was bunking the class.Asked question is from Antibiotics topic in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The CORRECT choice is (a) Partial cell recycling

To explain: D = F/V

DILUTION rate is the rate with which substrate is ADDED to a continuous system and products are removed from the system. When dilution rate is HIGHER than maximum GROWTH rate wash out condition occurs in which the cell concentrations progressively decreases. Only way of culturing biomass in the case of wash out is by partially recycling the cells, which were removed from the system.

39.

How does impeller speed affect bubble size?(a) As impeller speed increases, the bubble size increases(b) As impeller speed increases, bubble size stays consistent(c) As impeller speed increases, bubble size becomes inconsistent(d) As impeller speed increases, the bubble size decreasesI have been asked this question during an internship interview.Enquiry is from Antibiotics topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct choice is (d) As impeller speed increases, the bubble size decreases

To explain: As impeller speed increases shear and TURBULENCE increases, this decreases the bubble size. Large bubbles impedes in PROPER mixing of media. But SMALLER bubbles will give better mass TRANSFER.

40.

What may cause foaming in a bioreactor?(a) A decrease in agitation(b) The formation of large stable bubbles(c) The formation of small unstable bubbles(d) The breaking of large unstable bubblesThe question was asked in class test.My doubt stems from Antibiotics topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct answer is (d) The breaking of large unstable bubbles

Best explanation: Large WEAK foam bubbles are easily broken by MECHANICAL FORCES (i.e., agitation) and may FORM new tiny bubbles which are much more stable. Tiny bubbles has higher surface area to volume ratio which GIVES more mass transfer.

41.

What is the value of μmf / μf for fluidized bed fermenter?(a) 0.02 – 0.5(b) 0.05-0.08(c) 1.0-1.2(d) 0.0-0.02The question was asked during an interview.This intriguing question comes from Antibiotics topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct CHOICE is (a) 0.02 – 0.5

Best EXPLANATION: The substrate TENDS to MAKE lumps which adhere to the inner wall of the fermenter. This phenomenon causes an increase in the value of μmf. Thus, μmf / μf is actually estimated to be 0.02-0.5.

42.

Which microbes are used in photobioreactors?(a) Fungi(b) Bacteria(c) Microalgae(d) CyanobateriaThe question was posed to me in an interview for job.My doubt stems from Antibiotics topic in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right answer is (c) Microalgae

For EXPLANATION I would say: Photo-bioreactors are operated in a continuous mode at a TEMPERATURE RANGE of 25-40℃. Microalgae and cyanobacteria are used for this bioprocess most of the times. The organisms will be growing during day light while the products are produced during night.

43.

Why packed bed bioreactors are good?(a) Does not allow accumulation of products(b) Allow ease in pH controlling(c) Allow proper gas distribution(d) Less concentration of enzymes or cells required because of immobilisationI got this question in an online interview.The query is from Antibiotics in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct OPTION is (a) Does not allow accumulation of products

Explanation: It’s a difficult task to control the pH of packed BED BIOREACTORS by the adding ACID or alkali because of poor mixing. These bioreactors are preferred for bioprocessing technology involving product-inhibited reactions SINCE the packed bed bioreactors does not allow accumulation of the products.

44.

What is the most important thing one should remember while working with fluidized bed reactor?(a) Gas dispersion(b) Medium pH(c) Temperature(d) Weight of solid particlesThe question was posed to me by my school teacher while I was bunking the class.My question comes from Antibiotics topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The CORRECT answer is (d) Weight of solid particles

The explanation is: For an efficient operation of fluidized BEDS, gas is sparged to create a SUITABLE and optimised gas-liquid-solid fluid bed. It is necessary to KEEP in mind that the suspended solid particles are not too LIGHT or too dense (too light ones may float whereas to dense ones may settle at the bottom), and they should stay in a good suspended state.

45.

Two-stage airlift bioreactors are used for the temperature dependent formation of products.(a) True(b) FalseThis question was posed to me in my homework.I'm obligated to ask this question of Antibiotics topic in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right option is (a) True

For explanation I would SAY: In two-stage airlift bioreactors growing cells from one BIOREACTOR (maintained at temperature 30℃) are pumped into another bioreactor (at temperature 42°C). Since the temperature cannot be ABRUPTLY very QUICKLY increased from 30℃ to 42℃ there is a necessity for the two-stages.

46.

There are three types of airlift bioreactors.(a) True(b) FalseThe question was posed to me in an internship interview.My question comes from Antibiotics in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct answer is (b) False

Easiest explanation: Internal loop BIOREACTOR creates an internal LIQUID CIRCULATION channel. It has a SINGLE container and has a central draft tube that creates interior liquid circulation channel. External loop AIRLIFT bioreactor has an external loop where the liquid circulate through separate independent channels.

47.

Which of the following is a characteristic for airlift bioreactors?(a) More efficient than bubble column reactors(b) Less efficient than bubble column reactors(c) Equally efficient as bubble column reactors(d) Not at all efficientI got this question during an interview.My question comes from Antibiotics in portion Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct choice is (a) More EFFICIENT than bubble column reactors

The explanation: Airlift bioreactors are more efficient than bubble COLUMNS. This is particularly true for denser suspension of microorganisms. The mixing of the contents is BETTER than the bubble column than any other BIOREACTOR.

48.

What is the aspect ratio of bubble column bioreactors?(a) 1-3(b) 3-5(c) 4-6(d) 8-10I had been asked this question in semester exam.This question is from Antibiotics topic in section Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Right choice is (c) 4-6

To explain: Air or gas sparged inside a bioreactor such an AD BUBBLE column reactor through the use of PERFORATED pipes or plates are called spargers. The FLOW rate of the air/gas INFLUENCES the some factors —O2 transfer, mixing. The bubble column bioreactors may be fitted with perforated plates to improve its performance. The vessel used for bubble column bioreactors is usually cylindrical and has an aspect ratio of 4-6 (i.e., height to diameter ratio).

49.

Impellers in stirred tank bioreactors helps in ________________(a) Breaking down large bubbles into smaller ones(b) Mixing of medium contents(c) Homogenisation(d) Homogenisation, mixing, breaking bubblesThe question was asked in an international level competition.I'm obligated to ask this question of Antibiotics topic in chapter Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

The correct ANSWER is (d) Homogenisation, mixing, breaking bubbles

The explanation is: Bioreactors are CYLINDRICAL vessels with a motor driven shaft that supports one or more impellers or agitators. The bubbles which are generated by the sparger are bigger and has to be broken down to smaller bubbles by the USE of impellers. This LEADS to a UNIFORM and homogeneous environment throughout the bioreactor.

50.

Sparger in stirred tank bioreactor helps in ________________(a) Proper gas distribution(b) Proper mixing of medium(c) Measuring temperature of medium(d) Better sterilityThe question was asked by my school teacher while I was bunking the class.Question is taken from Antibiotics topic in division Antibiotics & Enzyme Immobilization of Drug Biotechnology

Answer»

Correct choice is (a) Proper gas distribution

The best explanation: A device known as the SPARGER is used to sparge in air inside a STIRRED tank reactor or a short stirred tank reactor. There are different kinds of sparger available. It can be ring with many holes, a tube with single orifice. Spargers and impellers enables BETTER gas distribution throughout the VESSEL.