Unit 3: Plant Bioactives, Single Cell Culture and Germplasm Preservation - Practice Quiz

BTY540 — Plant Biotechnology 60 Questions
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1 Single cell culture in plants involves the growth and multiplication of:

Techniques for single cell culture Easy
A. Individual isolated cells
B. Groups of tissues
C. Complete mature plants directly transferred without any isolation, sterilization, or nutrient adjustment steps
D. Whole intact organs

2 Which enzyme is commonly used to isolate single cells by degrading the middle lamella between plant cells?

Techniques for single cell culture Easy
A. Lipase
B. Pectinase
C. Amylase
D. Protease

3 Which method uses a very thin layer of medium in a dish to culture single cells?

Techniques for single cell culture Easy
A. Organ culture
B. Suspension culture
C. Callus culture
D. Micro-drop culture

4 Single cells obtained after enzymatic removal of the cell wall are called:

Techniques for single cell culture Easy
A. Meristems
B. Explants
C. Callus
D. Protoplasts

5 The technique in which single cells are grown on a layer of nurse cells is known as:

Techniques for single cell culture Easy
A. Batch culture
B. Static culture
C. Nurse culture
D. Hanging drop culture

6 Single cell culture is especially useful for producing:

Applications of single cell culture Easy
A. Grafted plants
B. Genetically uniform clones
C. Wild-type ecotypes
D. Naturally cross-pollinated hybrids

7 Which of the following is an important application of single cell culture?

Applications of single cell culture Easy
A. Field irrigation
B. Soil testing
C. Mutant selection
D. Seed drying

8 Single cell culture helps study the process of __ at the individual cell level.

Applications of single cell culture Easy
A. Root gravitropism in soil
B. Photosynthesis in whole forests
C. Seed germination in nature
D. Cell division and differentiation

9 Single cells that can develop into complete plants demonstrate the property of:

Applications of single cell culture Easy
A. Dormancy
B. Senescence
C. Necrosis
D. Totipotency

10 Secondary metabolites in plants are mainly produced using:

Techniques of secondary metabolite production Easy
A. Bacterial fermentation only
B. Cell suspension cultures
C. Whole plantations only
D. Animal cell lines

11 The addition of a compound that stimulates increased production of a secondary metabolite is called:

Techniques of secondary metabolite production Easy
A. Sterilization
B. Acclimatization
C. Elicitation
D. Subculturing

12 Which cultured organ system is often used to produce secondary metabolites due to genetic stability?

Techniques of secondary metabolite production Easy
A. Pollen tubes
B. Hairy root cultures
C. Xylem vessels
D. Guard cells

13 Large-scale culturing of plant cells for metabolite production is typically carried out in a:

Techniques of secondary metabolite production Easy
A. Bioreactor
B. Seed bank
C. Greenhouse pot
D. Petri dish only

14 Many plant secondary metabolites are commercially important as:

Applications of secondary metabolites and bioactives Easy
A. Pharmaceutical drugs
B. Metal alloys
C. Building cement
D. Plastic polymers

15 Which anticancer secondary metabolite is obtained from Taxus species?

Applications of secondary metabolites and bioactives Easy
A. Taxol
B. Caffeine
C. Nicotine
D. Morphine

16 Plant bioactives are commonly used in the food industry as natural:

Applications of secondary metabolites and bioactives Easy
A. Fertilizers and pesticides only
B. Flavors and colors
C. Construction materials
D. Fuels and lubricants

17 A cryoprotectant is a substance used to:

Germplasm preservation methods: cryoprotectants Easy
A. Increase enzyme activity at high temperature
B. Kill microbial contaminants
C. Protect cells from freezing damage
D. Speed up plant flowering

18 Which of the following is a commonly used cryoprotectant?

Germplasm preservation methods: cryoprotectants Easy
A. Dimethyl sulfoxide (DMSO)
B. Ethanol only
C. Acetic acid
D. Sodium chloride

19 Cryopreservation of plant germplasm is generally carried out in liquid nitrogen at approximately:

Germplasm preservation methods: cryopreservation Easy
A.
B.
C.
D.

20 Which storage method is considered best for long-term preservation of plant germplasm?

Germplasm preservation methods: long term storage Easy
A. Storage at room temperature
B. Short-term refrigeration at with occasional subculturing every few weeks
C. Drying in open air
D. Cryopreservation

21 A researcher wants to isolate single cells from intact leaf mesophyll tissue without using enzymes. Which technique is most appropriate?

techniques for single cell culture Medium
A. Protoplast fusion using PEG
B. Sequential digestion with macerozyme
C. Mechanical isolation by grinding tissue in a suitable buffer
D. Treatment with pectinase and cellulase

22 In the feeder layer technique for culturing single cells at low density, what is the primary role of the feeder layer?

techniques for single cell culture Medium
A. To supply conditioning factors and growth substances that support the isolated cell
B. To act as a source of contamination control
C. To provide light for photosynthesis
D. To physically anchor the single cell to the medium

23 The Bergmann cell plating technique is primarily used to:

techniques for single cell culture Medium
A. Preserve germplasm at low temperature
B. Fuse two protoplasts
C. Extract secondary metabolites
D. Determine plating efficiency and isolate single-cell clones

24 Which culture method keeps a single cell in a very small volume of medium in a microchamber, allowing continuous microscopic observation of its division?

techniques for single cell culture Medium
A. Microchamber (micro-drop) technique
B. Bergmann plating
C. Suspension culture in shake flasks
D. Nurse culture on filter paper

25 Single cell cloning is valuable in plant biotechnology mainly because it allows:

applications of single cell culture Medium
A. Direct field transplantation of protoplasts
B. Formation of somatic hybrids without fusion
C. Production of grafted chimeras
D. Selection of genetically uniform mutant lines from individual cells

26 In a mutant selection program, single cells are grown on medium containing a selective agent (e.g., an amino acid analogue). The surviving colonies are most likely:

applications of single cell culture Medium
A. Non-dividing feeder cells
B. Cells that lost their cell wall permanently
C. Cells contaminated with bacteria
D. Cells carrying resistance mutations to the selective agent

27 Which application relies on the totipotency demonstrated by single plant cells?

applications of single cell culture Medium
A. Grafting of two woody stems
B. Extraction of chlorophyll from leaves
C. Fermentation of glucose to ethanol
D. Regeneration of a whole plant from a single cultured cell

28 In cell suspension cultures, a two-stage (growth and production) strategy is often used because:

techniques of secondary metabolite production Medium
A. Cells cannot grow and photosynthesise simultaneously
B. Metabolites are only made during log phase growth
C. Secondary metabolite synthesis frequently peaks after the growth phase slows
D. The first stage removes all contaminants

29 Adding a precursor such as phenylalanine to a culture producing rosmarinic acid is an example of:

techniques of secondary metabolite production Medium
A. Immobilization of cells
B. Precursor feeding to enhance metabolite yield
C. Cryoprotection of the culture
D. Elicitation using a biotic agent

30 Treating a cell culture with a fungal cell-wall extract to boost alkaloid production is called:

techniques of secondary metabolite production Medium
A. Subculturing
B. Encapsulation
C. Elicitation
D. Immobilization

31 Why are hairy root cultures (via Agrobacterium rhizogenes) often preferred for producing certain secondary metabolites?

techniques of secondary metabolite production Medium
A. They require no nutrients
B. They cannot be scaled up
C. They are genetically stable and produce metabolites at levels comparable to intact roots
D. They grow only in the dark without medium

32 Cell immobilization in calcium alginate beads benefits secondary metabolite production mainly by:

techniques of secondary metabolite production Medium
A. Increasing the mutation rate of cells
B. Eliminating the need for a carbon source
C. Preventing any metabolite synthesis
D. Allowing continuous product recovery and prolonged cell viability

33 Which pairing of a plant secondary metabolite with its commercial use is correct?

applications of secondary metabolites and bioactives Medium
A. Starch — analgesic
B. Lignin — antimalarial
C. Taxol — anticancer drug
D. Cellulose — antibiotic

34 Shikonin, produced commercially from Lithospermum cell cultures, is valued mainly as a:

applications of secondary metabolites and bioactives Medium
A. Natural dye and antimicrobial/wound-healing pigment
B. Photosynthetic pigment for food colour only
C. Nitrogen-fixing compound
D. Structural cell-wall polymer

35 A pharmaceutical company chooses cell culture rather than field cultivation to obtain a bioactive alkaloid. Which is the strongest justification?

applications of secondary metabolites and bioactives Medium
A. Consistent, season-independent supply under controlled conditions
B. The metabolite structure changes to a simpler form
C. It always costs less than any field crop
D. It removes the need for any downstream purification

36 DMSO and glycerol are commonly used cryoprotectants because they:

cryoprotectants Medium
A. Kill microbial contaminants
B. Increase the freezing point of water
C. Reduce intracellular ice-crystal formation during freezing
D. Supply carbon for cell growth

37 Which statement best distinguishes a penetrating from a non-penetrating cryoprotectant?

cryoprotectants Medium
A. Both act only outside the cell
B. Penetrating agents (e.g., DMSO) enter cells, while non-penetrating agents (e.g., sucrose) act osmotically outside
C. Both are toxic and never used
D. Penetrating agents stay outside, non-penetrating enter cells

38 In the vitrification method of cryopreservation, cells are protected because:

cryopreservation Medium
A. Water content is increased before freezing
B. Cells are frozen slowly to form large crystals
C. Highly concentrated cryoprotectants form a glassy solid without ice crystals
D. Cells are heated above 100 °C

39 Cryopreserved plant material is typically stored in liquid nitrogen. The corresponding temperature is approximately:

cryopreservation Medium
A.
B.
C.
D.

40 For short/medium-term in vitro conservation, growth is slowed by reduced temperature and osmotic agents. Which addition most directly slows growth osmotically?

short or Medium term storage Medium
A. Extra auxin in the medium
B. Increased light intensity
C. Mannitol in the culture medium
D. Higher incubation temperature

41 In the Bergmann cell plating technique, a single cell suspension is mixed with molten agar medium and poured into a Petri dish. If the plating efficiency is defined as the ratio of colonies formed to cells plated, and a researcher plates cells and obtains 1600 colonies, what is the plating efficiency, and what does a low value primarily indicate?

techniques for single cell culture Hard
A. ; indicating optimal nurse tissue support was provided
B. ; indicating the cells were fully differentiated and non-dividing
C. ; indicating many cells failed to divide due to lack of conditioning factors or low density
D. ; indicating the agar concentration was toxic to all cells

42 A researcher wants to culture a single isolated cell without diluting the conditioning factors it secretes. Which technique best achieves cell growth at effectively 'high density' for the individual cell while keeping it physically isolated?

techniques for single cell culture Hard
A. Bergmann agar plating at cells/mL
B. Filter paper raft nurse technique with pooled medium exchange
C. Bulk suspension culture in a large stirred bioreactor
D. Microchamber / microdrop culture (Torrey's technique) using a small volume

43 Single cell cloning is exploited to isolate somaclonal variants. Which statement most accurately describes why single-cell-derived clones are preferred over shoot-tip derived plants for capturing novel variation?

applications of single cell culture Hard
A. Single cells always retain the exact parental genotype ensuring uniformity
B. Shoot tips undergo meiosis producing more variation than somatic cells
C. Single cells cannot be regenerated so variation is irrelevant
D. Single cells expose recessive mutations and epigenetic changes uniformly across the regenerant, avoiding chimeras

44 In a two-stage batch culture for secondary metabolite production, cells are first grown in a growth medium then transferred to a production medium. Why is this two-stage strategy often necessary?

techniques of secondary metabolite production Hard
A. Growth and metabolite production peak simultaneously in log phase
B. Secondary metabolite synthesis is typically maximal during the stationary/idiophase and can be inhibited by rapid growth conditions
C. Primary metabolites are only produced during stationary phase requiring separation
D. Cells cannot survive in a single medium beyond 24 hours

45 Elicitation is used to boost secondary metabolite yield. A biotic elicitor such as a fungal cell wall fragment (e.g., chitosan) primarily enhances metabolite production by:

techniques of secondary metabolite production Hard
A. Mimicking a pathogen attack and triggering defense-related signal transduction and gene expression
B. Increasing the osmotic potential to lyse vacuoles and release products
C. Permanently mutating biosynthetic genes to overexpress them
D. Providing additional carbon skeletons directly incorporated into the metabolite

46 In-situ product removal (ISPR) using adsorbent resins or a second organic phase is applied during metabolite production mainly to overcome which limitation?

techniques of secondary metabolite production Hard
A. Feedback/end-product inhibition and degradation of the accumulated metabolite
B. Excessive foaming during aeration
C. Lack of precursor availability in the medium
D. Insufficient oxygen transfer in the bioreactor

47 Shikonin was the first plant secondary metabolite commercially produced via cell suspension culture. Which combination of factors made this economically viable compared to other metabolites?

applications of secondary metabolites and bioactives Hard
A. Its production required no medium optimization or elicitation
B. High market value, high per-cell productivity, and a two-stage medium optimized for accumulation
C. Low market value but extremely simple extraction from field crops
D. It is a primary metabolite produced constitutively in all growth phases

48 Hairy root cultures induced by Agrobacterium rhizogenes are often superior to cell suspension cultures for producing certain alkaloids because they:

applications of secondary metabolites and bioactives Hard
A. Grow faster than undifferentiated callus in all cases
B. Require no phytohormones but produce only primary metabolites
C. Lose the Ri plasmid rapidly ensuring genetic reversion
D. Are genetically and biochemically stable and can synthesize metabolites normally made in differentiated roots

49 Cryoprotectants are classified as penetrating and non-penetrating. DMSO (penetrating) and sucrose (non-penetrating) are often combined. What is the principal complementary mechanism of this combination?

cryoprotectants Hard
A. Both act only extracellularly to form a protective sugar glass
B. DMSO reduces intracellular ice by entering cells while sucrose drives osmotic dehydration, together minimizing lethal ice formation
C. Both increase intracellular water content to dilute salts
D. DMSO raises the freezing point while sucrose lowers membrane permeability

50 During vitrification-based cryopreservation, a highly concentrated cryoprotectant mixture (e.g., PVS2) is applied. The primary goal of vitrification is to:

cryoprotectants Hard
A. Increase the freezing point so cells freeze at higher temperatures
B. Convert cell water into an amorphous glass state without ice crystal formation on cooling
C. Promote controlled extracellular ice nucleation to dehydrate cells slowly
D. Rehydrate cells fully before plunging into liquid nitrogen

51 Excessively high DMSO concentrations or prolonged exposure at room temperature before freezing can be detrimental because DMSO:

cryoprotectants Hard
A. Is cytotoxic and can cause osmotic stress and chemical toxicity if not applied cold and briefly
B. Permanently crosslinks DNA at all temperatures
C. Freezes irreversibly at blocking cell metabolism
D. Cannot penetrate the plasma membrane at any temperature

52 In the classical two-step (slow) freezing protocol, samples are cooled at a controlled rate (e.g., ) to about before plunging into liquid nitrogen. The controlled slow cooling step is critical because it:

cryopreservation Hard
A. Prevents any water loss to preserve full cell turgor
B. Forces intracellular ice to nucleate uniformly for even freezing
C. Allows extracellular ice formation and progressive protective dehydration, minimizing intracellular ice
D. Warms the cytoplasm to prevent solute concentration

53 Rapid, uncontrolled warming (thawing) after cryopreservation is generally recommended for slow-frozen plant cells to prevent:

cryopreservation Hard
A. Recrystallization (devitrification) where small ice crystals fuse into large damaging ones
B. Immediate cryoprotectant precipitation on the membrane
C. Loss of the amorphous glass state in vitrified samples only
D. Osmotic swelling from cryoprotectant influx

54 Encapsulation-dehydration is a cryopreservation technique where explants are encased in alginate beads. The key advantage of this approach over direct vitrification is that it:

cryopreservation Hard
A. Freezes samples at without any dehydration
B. Allows gradual osmotic and evaporative dehydration with reduced toxic cryoprotectant exposure
C. Eliminates the need for liquid nitrogen entirely
D. Guarantees regrowth for all species without optimization

55 For medium-term germplasm storage, growth is slowed rather than stopped. Which combination of methods is most consistent with achieving reduced-growth in-vitro storage?

short or Medium term storage Hard
A. Cryopreservation in liquid nitrogen at
B. Continuous high-light incubation at with rich medium
C. Complete desiccation of seeds to moisture
D. Lowering temperature (–), adding osmotica like mannitol, and reducing nutrient/hormone levels

56 A key limitation of reduced-growth (medium-term) storage compared to cryopreservation is that:

short or Medium term storage Hard
A. Metabolism is completely halted preventing all genetic change
B. It requires liquid nitrogen infrastructure that is costly
C. Samples cannot be recovered once stored
D. Cells remain metabolically active, so somaclonal variation and genetic drift can still accumulate over repeated subcultures

57 'Recalcitrant' seeds (e.g., many tropical species) cannot be conserved in conventional seed banks. The main reason and the recommended long-term alternative are:

long term storage Hard
A. They have thick coats blocking imbibition; scarification and drying is used
B. They germinate too fast; short-term cold storage of whole seeds is used
C. They produce toxins; in-vitro suspension culture is used long-term
D. They cannot tolerate desiccation/low temperature; cryopreservation of excised embryonic axes is used instead

58 Liquid nitrogen storage at is considered ideal for long-term germplasm conservation primarily because at this temperature:

long term storage Hard
A. Cells continue slow division to maintain viability signals
B. All metabolic and most physicochemical (diffusion-driven) reactions effectively cease, halting deterioration indefinitely
C. Enzymatic repair of DNA is accelerated preventing mutations
D. Ice crystals grow slowly enough to remain harmless

59 Protoplast fusion followed by single-cell culture is used for somatic hybridization. If a fusion produces a heterokaryon that later loses chromosomes from one parent during culture, the resulting product is best described as a:

applications of single cell culture Hard
A. Non-viable cell that cannot regenerate
B. Asymmetric hybrid / cybrid depending on which genome components are retained
C. Perfect symmetric amphidiploid with all chromosomes retained
D. Haploid regenerant identical to one parent

60 Precursor feeding is a strategy to enhance secondary metabolite yield. For it to be effective, the fed precursor must:

techniques of secondary metabolite production Hard
A. Be a primary metabolite unrelated to the target pathway
B. Be a final end-product that feedback-activates the pathway
C. Lie on the biosynthetic pathway at a step that is rate-limiting or committed toward the target product
D. Inhibit all competing branch pathways permanently