Liquid nitrogen maintains a temperature of about , which halts metabolic activity for long-term storage.
Incorrect! Try again.
20Which storage method is considered best for long-term preservation of plant germplasm?
Germplasm preservation methods: long term storage
Easy
A.Drying in open air
B.Cryopreservation
C.Short-term refrigeration at with occasional subculturing every few weeks
D.Storage at room temperature
Correct Answer: Cryopreservation
Explanation:
Cryopreservation in liquid nitrogen allows indefinite, stable long-term storage of germplasm without genetic change.
Incorrect! Try again.
21A 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.Mechanical isolation by grinding tissue in a suitable buffer
B.Protoplast fusion using PEG
C.Treatment with pectinase and cellulase
D.Sequential digestion with macerozyme
Correct Answer: Mechanical isolation by grinding tissue in a suitable buffer
Explanation:
Single cells can be freed from soft tissues like mesophyll by gentle mechanical maceration in buffer, avoiding enzymes. Pectinase, cellulase and macerozyme are enzymatic methods, and PEG is used for protoplast fusion.
Incorrect! Try again.
22In 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 physically anchor the single cell to the medium
B.To provide light for photosynthesis
C.To supply conditioning factors and growth substances that support the isolated cell
D.To act as a source of contamination control
Correct Answer: To supply conditioning factors and growth substances that support the isolated cell
Explanation:
A feeder layer (X-irradiated non-dividing cells) releases metabolites and conditioning factors that enable a single isolated cell to divide at very low plating densities.
Incorrect! Try again.
23The Bergmann cell plating technique is primarily used to:
techniques for single cell culture
Medium
A.Fuse two protoplasts
B.Preserve germplasm at low temperature
C.Extract secondary metabolites
D.Determine plating efficiency and isolate single-cell clones
Correct Answer: Determine plating efficiency and isolate single-cell clones
Explanation:
Bergmann's plating distributes single cells evenly in a thin layer of agar-solidified medium, allowing colonies to arise from single cells and enabling calculation of plating efficiency.
Incorrect! Try again.
24Which culture method keeps a single cell in a very small volume of medium in a microchamber, allowing continuous microscopic observation of its division?
The microchamber technique isolates a single cell in a tiny drop of medium sealed between slides, permitting direct microscopic tracking of its growth and division.
Incorrect! Try again.
25Single cell cloning is valuable in plant biotechnology mainly because it allows:
applications of single cell culture
Medium
A.Selection of genetically uniform mutant lines from individual cells
B.Production of grafted chimeras
C.Direct field transplantation of protoplasts
D.Formation of somatic hybrids without fusion
Correct Answer: Selection of genetically uniform mutant lines from individual cells
Explanation:
Because each clone originates from one cell, single cell culture is ideal for isolating and multiplying genetically uniform variants or mutants selected in vitro.
Incorrect! Try again.
26In 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 carrying resistance mutations to the selective agent
C.Cells that lost their cell wall permanently
D.Cells contaminated with bacteria
Correct Answer: Cells carrying resistance mutations to the selective agent
Explanation:
Selection pressure kills sensitive cells, so surviving colonies represent variants that acquired resistance to the toxic analogue, allowing recovery of desired mutant genotypes.
Incorrect! Try again.
27Which application relies on the totipotency demonstrated by single plant cells?
applications of single cell culture
Medium
A.Regeneration of a whole plant from a single cultured cell
B.Fermentation of glucose to ethanol
C.Extraction of chlorophyll from leaves
D.Grafting of two woody stems
Correct Answer: Regeneration of a whole plant from a single cultured cell
Explanation:
Totipotency is the ability of a single somatic cell to regenerate an entire organism; single cell culture exploits this to raise complete plants from one cell.
Incorrect! Try again.
28In cell suspension cultures, a two-stage (growth and production) strategy is often used because:
techniques of secondary metabolite production
Medium
A.Metabolites are only made during log phase growth
B.Secondary metabolite synthesis frequently peaks after the growth phase slows
C.Cells cannot grow and photosynthesise simultaneously
D.The first stage removes all contaminants
Correct Answer: Secondary metabolite synthesis frequently peaks after the growth phase slows
Explanation:
Many secondary metabolites accumulate during the stationary/production phase, so a growth medium is used first, then cells are shifted to a production medium optimised for metabolite synthesis.
Incorrect! Try again.
29Adding 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.Cryoprotection of the culture
C.Elicitation using a biotic agent
D.Precursor feeding to enhance metabolite yield
Correct Answer: Precursor feeding to enhance metabolite yield
Explanation:
Supplying a biosynthetic intermediate (precursor) pushes the pathway toward the desired product, increasing yield — a common precursor-feeding strategy.
Incorrect! Try again.
30Treating a cell culture with a fungal cell-wall extract to boost alkaloid production is called:
techniques of secondary metabolite production
Medium
A.Elicitation
B.Encapsulation
C.Immobilization
D.Subculturing
Correct Answer: Elicitation
Explanation:
Elicitors (biotic like fungal extracts, or abiotic like metal ions) trigger the plant's defence-related secondary metabolism, enhancing production of compounds such as alkaloids and phytoalexins.
Incorrect! Try again.
31Why are hairy root cultures (via Agrobacterium rhizogenes) often preferred for producing certain secondary metabolites?
techniques of secondary metabolite production
Medium
A.They grow only in the dark without medium
B.They are genetically stable and produce metabolites at levels comparable to intact roots
C.They require no nutrients
D.They cannot be scaled up
Correct Answer: They are genetically stable and produce metabolites at levels comparable to intact roots
Explanation:
Hairy roots show fast, hormone-independent growth, are genetically stable, and synthesise root-associated metabolites at levels similar to or above those of the parent plant.
Incorrect! Try again.
32Cell immobilization in calcium alginate beads benefits secondary metabolite production mainly by:
techniques of secondary metabolite production
Medium
A.Preventing any metabolite synthesis
B.Increasing the mutation rate of cells
C.Eliminating the need for a carbon source
D.Allowing continuous product recovery and prolonged cell viability
Correct Answer: Allowing continuous product recovery and prolonged cell viability
Explanation:
Immobilized cells remain in a differentiated, viable state longer and permit continuous (non-destructive) product removal, improving process efficiency.
Incorrect! Try again.
33Which pairing of a plant secondary metabolite with its commercial use is correct?
applications of secondary metabolites and bioactives
Medium
A.Taxol — anticancer drug
B.Starch — analgesic
C.Cellulose — antibiotic
D.Lignin — antimalarial
Correct Answer: Taxol — anticancer drug
Explanation:
Taxol (paclitaxel), a diterpenoid alkaloid from Taxus, is a well-known anticancer agent. The other molecules are structural/storage polymers, not the therapeutics listed.
Incorrect! Try again.
34Shikonin, produced commercially from Lithospermum cell cultures, is valued mainly as a:
applications of secondary metabolites and bioactives
Medium
A.Nitrogen-fixing compound
B.Structural cell-wall polymer
C.Photosynthetic pigment for food colour only
D.Natural dye and antimicrobial/wound-healing pigment
Correct Answer: Natural dye and antimicrobial/wound-healing pigment
Explanation:
Shikonin is a red naphthoquinone pigment with antimicrobial and anti-inflammatory properties; it was among the first secondary metabolites produced commercially by plant cell culture.
Incorrect! Try again.
35A 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.The metabolite structure changes to a simpler form
B.Consistent, season-independent supply under controlled conditions
C.It removes the need for any downstream purification
D.It always costs less than any field crop
Correct Answer: Consistent, season-independent supply under controlled conditions
Explanation:
Cell cultures give a controlled, continuous, climate-independent source of the compound with uniform quality — a key advantage over seasonal, variable field production.
Incorrect! Try again.
36DMSO and glycerol are commonly used cryoprotectants because they:
cryoprotectants
Medium
A.Supply carbon for cell growth
B.Increase the freezing point of water
C.Kill microbial contaminants
D.Reduce intracellular ice-crystal formation during freezing
Correct Answer: Reduce intracellular ice-crystal formation during freezing
Explanation:
Cryoprotectants like DMSO and glycerol lower the freezing point and limit lethal intracellular ice crystal formation and dehydration damage during cryopreservation.
Incorrect! Try again.
37Which statement best distinguishes a penetrating from a non-penetrating cryoprotectant?
cryoprotectants
Medium
A.Both act only outside the cell
B.Both are toxic and never used
C.Penetrating agents (e.g., DMSO) enter cells, while non-penetrating agents (e.g., sucrose) act osmotically outside
D.Penetrating agents stay outside, non-penetrating enter cells
Correct Answer: Penetrating agents (e.g., DMSO) enter cells, while non-penetrating agents (e.g., sucrose) act osmotically outside
Explanation:
Penetrating cryoprotectants such as DMSO and glycerol cross the membrane to protect internally, whereas non-penetrating ones like sucrose and PEG act by drawing out water osmotically.
Incorrect! Try again.
38In the vitrification method of cryopreservation, cells are protected because:
cryopreservation
Medium
A.Highly concentrated cryoprotectants form a glassy solid without ice crystals
B.Water content is increased before freezing
C.Cells are heated above 100 °C
D.Cells are frozen slowly to form large crystals
Correct Answer: Highly concentrated cryoprotectants form a glassy solid without ice crystals
Explanation:
Vitrification uses highly concentrated cryoprotectant solutions and rapid cooling so the cell contents solidify into a glass-like state, avoiding damaging ice-crystal formation.
Incorrect! Try again.
39Cryopreserved plant material is typically stored in liquid nitrogen. The corresponding temperature is approximately:
cryopreservation
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
Liquid nitrogen maintains about , at which all metabolic and most physicochemical processes cease, permitting long-term genetic stability.
Incorrect! Try again.
40For 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.Higher incubation temperature
B.Mannitol in the culture medium
C.Increased light intensity
D.Extra auxin in the medium
Correct Answer: Mannitol in the culture medium
Explanation:
Osmotic retardants like mannitol or sorbitol reduce water availability and slow metabolism, extending subculture intervals for medium-term storage without freezing.
Incorrect! Try again.
41In 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
Correct Answer: ; indicating many cells failed to divide due to lack of conditioning factors or low density
Explanation:
Plating efficiency . Low plating efficiency at limiting cell densities typically reflects insufficient conditioning factors, which is why nurse cultures or conditioned medium are used to support isolated single cells.
Incorrect! Try again.
42A 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.Microchamber / microdrop culture (Torrey's technique) using a small volume
C.Bulk suspension culture in a large stirred bioreactor
D.Filter paper raft nurse technique with pooled medium exchange
Correct Answer: Microchamber / microdrop culture (Torrey's technique) using a small volume
Explanation:
In microchamber/microdrop culture, a single cell is placed in a very small volume so its own secreted conditioning factors are not diluted, mimicking high-density conditions while allowing observation of a single isolated cell.
Incorrect! Try again.
43Single 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 expose recessive mutations and epigenetic changes uniformly across the regenerant, avoiding chimeras
B.Single cells cannot be regenerated so variation is irrelevant
C.Single cells always retain the exact parental genotype ensuring uniformity
D.Shoot tips undergo meiosis producing more variation than somatic cells
Correct Answer: Single cells expose recessive mutations and epigenetic changes uniformly across the regenerant, avoiding chimeras
Explanation:
A plant regenerated from a single cell is non-chimeric, so any mutation (including recessive) or epigenetic change is present throughout, allowing clean recovery and expression of somaclonal variants, unlike multicellular explants that yield chimeras.
Incorrect! Try again.
44In 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.Cells cannot survive in a single medium beyond 24 hours
C.Primary metabolites are only produced during stationary phase requiring separation
D.Secondary metabolite synthesis is typically maximal during the stationary/idiophase and can be inhibited by rapid growth conditions
Correct Answer: Secondary metabolite synthesis is typically maximal during the stationary/idiophase and can be inhibited by rapid growth conditions
Explanation:
Many secondary metabolites accumulate in the idiophase (stationary phase) and are inversely related to growth. A growth-optimized medium builds biomass; a production medium (often high sucrose, low nitrogen, altered hormones) then triggers metabolite accumulation.
Incorrect! Try again.
45Elicitation 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.Providing additional carbon skeletons directly incorporated into the metabolite
D.Permanently mutating biosynthetic genes to overexpress them
Correct Answer: Mimicking a pathogen attack and triggering defense-related signal transduction and gene expression
Explanation:
Biotic elicitors like chitosan act as pathogen-associated molecular patterns, activating defense signaling (jasmonate, salicylate pathways) that upregulate biosynthetic genes for defensive secondary metabolites, thereby increasing yield.
Incorrect! Try again.
46In-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.Insufficient oxygen transfer in the bioreactor
B.Feedback/end-product inhibition and degradation of the accumulated metabolite
C.Lack of precursor availability in the medium
D.Excessive foaming during aeration
Correct Answer: Feedback/end-product inhibition and degradation of the accumulated metabolite
Explanation:
Continuous removal of the product prevents it from reaching concentrations that cause feedback inhibition or that degrade/are toxic to cells, thereby sustaining higher net production over time.
Incorrect! Try again.
47Shikonin 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.Low market value but extremely simple extraction from field crops
C.High market value, high per-cell productivity, and a two-stage medium optimized for accumulation
D.It is a primary metabolite produced constitutively in all growth phases
Correct Answer: High market value, high per-cell productivity, and a two-stage medium optimized for accumulation
Explanation:
Shikonin (from Lithospermum erythrorhizon) commanded a high price and was produced at high yield using an optimized two-stage system, making cell-culture production cost-effective—unlike many low-value metabolites where field cultivation is cheaper.
Incorrect! Try again.
48Hairy 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.Require no phytohormones but produce only primary metabolites
B.Grow faster than undifferentiated callus in all cases
C.Are genetically and biochemically stable and can synthesize metabolites normally made in differentiated roots
D.Lose the Ri plasmid rapidly ensuring genetic reversion
Correct Answer: Are genetically and biochemically stable and can synthesize metabolites normally made in differentiated roots
Explanation:
Hairy roots retain organ-level differentiation and metabolic stability, enabling continuous synthesis of root-associated metabolites (e.g., tropane alkaloids) without hormones, unlike genetically unstable, dedifferentiated suspension cells.
Incorrect! Try again.
49Cryoprotectants 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 increase intracellular water content to dilute salts
B.Both act only extracellularly to form a protective sugar glass
C.DMSO reduces intracellular ice by entering cells while sucrose drives osmotic dehydration, together minimizing lethal ice formation
D.DMSO raises the freezing point while sucrose lowers membrane permeability
Correct Answer: DMSO reduces intracellular ice by entering cells while sucrose drives osmotic dehydration, together minimizing lethal ice formation
Explanation:
Penetrating agents (DMSO) enter cells and colligatively reduce intracellular ice; non-penetrating agents (sucrose) stay outside and osmotically dehydrate cells. Combined, they lower the amount of freezable intracellular water, reducing ice-crystal damage.
Incorrect! Try again.
50During 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
Correct Answer: Convert cell water into an amorphous glass state without ice crystal formation on cooling
Explanation:
Vitrification uses highly concentrated cryoprotectants and rapid cooling so cellular solutions solidify into a non-crystalline (glassy) state, avoiding the mechanical damage caused by ice crystals entirely, bypassing slow controlled freezing.
Incorrect! Try again.
51Excessively high DMSO concentrations or prolonged exposure at room temperature before freezing can be detrimental because DMSO:
cryoprotectants
Hard
A.Cannot penetrate the plasma membrane at any temperature
B.Permanently crosslinks DNA at all temperatures
C.Freezes irreversibly at blocking cell metabolism
D.Is cytotoxic and can cause osmotic stress and chemical toxicity if not applied cold and briefly
Correct Answer: Is cytotoxic and can cause osmotic stress and chemical toxicity if not applied cold and briefly
Explanation:
DMSO is chemically toxic and osmotically active. To limit damage it is added at low temperature (often ) and for short durations before freezing, balancing its cryoprotective benefit against toxicity.
Incorrect! Try again.
52In 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.Warms the cytoplasm to prevent solute concentration
Slow cooling causes ice to form first outside the cell; the resulting osmotic gradient draws water out, dehydrating the cell so that lethal intracellular ice is minimized before final rapid plunge into liquid nitrogen.
Incorrect! Try again.
53Rapid, uncontrolled warming (thawing) after cryopreservation is generally recommended for slow-frozen plant cells to prevent:
cryopreservation
Hard
A.Osmotic swelling from cryoprotectant influx
B.Recrystallization (devitrification) where small ice crystals fuse into large damaging ones
C.Loss of the amorphous glass state in vitrified samples only
D.Immediate cryoprotectant precipitation on the membrane
Correct Answer: Recrystallization (devitrification) where small ice crystals fuse into large damaging ones
Explanation:
During slow warming, tiny intracellular ice crystals can grow/recrystallize into larger crystals that rupture membranes. Rapid warming passes through this dangerous temperature zone quickly, reducing recrystallization damage.
Incorrect! Try again.
54Encapsulation-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.Guarantees regrowth for all species without optimization
B.Freezes samples at without any dehydration
C.Allows gradual osmotic and evaporative dehydration with reduced toxic cryoprotectant exposure
D.Eliminates the need for liquid nitrogen entirely
Correct Answer: Allows gradual osmotic and evaporative dehydration with reduced toxic cryoprotectant exposure
Explanation:
In encapsulation-dehydration, alginate-encased explants are pre-cultured in high sucrose then air/silica-dried, achieving tolerance to freezing with minimal exposure to toxic penetrating cryoprotectants, unlike PVS2-based vitrification.
Incorrect! Try again.
55For 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.Complete desiccation of seeds to moisture
B.Lowering temperature (–), adding osmotica like mannitol, and reducing nutrient/hormone levels
C.Cryopreservation in liquid nitrogen at
D.Continuous high-light incubation at with rich medium
Correct Answer: Lowering temperature (–), adding osmotica like mannitol, and reducing nutrient/hormone levels
Explanation:
Medium-term (reduced-growth) storage extends subculture intervals by slowing metabolism using low temperatures, osmotic/growth-retarding agents (mannitol, ABA), and nutrient-limited media, without the full metabolic arrest of cryopreservation.
Incorrect! Try again.
56A key limitation of reduced-growth (medium-term) storage compared to cryopreservation is that:
short or Medium term storage
Hard
A.Cells remain metabolically active, so somaclonal variation and genetic drift can still accumulate over repeated subcultures
B.It requires liquid nitrogen infrastructure that is costly
C.Metabolism is completely halted preventing all genetic change
D.Samples cannot be recovered once stored
Correct Answer: Cells remain metabolically active, so somaclonal variation and genetic drift can still accumulate over repeated subcultures
Explanation:
Because reduced-growth storage only slows (not stops) metabolism and cells still divide occasionally, mutations and somaclonal variation can accumulate over time—unlike cryopreservation, which arrests metabolism and preserves genetic stability.
Incorrect! Try again.
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 germinate too fast; short-term cold storage of whole seeds is used
B.They cannot tolerate desiccation/low temperature; cryopreservation of excised embryonic axes is used instead
C.They have thick coats blocking imbibition; scarification and drying is used
D.They produce toxins; in-vitro suspension culture is used long-term
Correct Answer: They cannot tolerate desiccation/low temperature; cryopreservation of excised embryonic axes is used instead
Explanation:
Recalcitrant seeds are desiccation-sensitive and die when dried/frozen as whole seeds. For long-term conservation, embryonic axes or embryos are excised, partially dried, and cryopreserved in liquid nitrogen.
Incorrect! Try again.
58Liquid 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.Ice crystals grow slowly enough to remain harmless
C.Enzymatic repair of DNA is accelerated preventing mutations
D.All metabolic and most physicochemical (diffusion-driven) reactions effectively cease, halting deterioration indefinitely
Correct Answer: All metabolic and most physicochemical (diffusion-driven) reactions effectively cease, halting deterioration indefinitely
Explanation:
At (below the glass transition of water) liquid water and molecular diffusion are essentially absent, so metabolic and deleterious chemical reactions stop, allowing theoretically indefinite storage with genetic stability.
Incorrect! Try again.
59Protoplast 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.Perfect symmetric amphidiploid with all chromosomes retained
B.Non-viable cell that cannot regenerate
C.Asymmetric hybrid / cybrid depending on which genome components are retained
D.Haploid regenerant identical to one parent
Correct Answer: Asymmetric hybrid / cybrid depending on which genome components are retained
Explanation:
When a fused cell loses part of one parent's nuclear genome, it becomes an asymmetric somatic hybrid; if one nuclear genome is lost but cytoplasm/organelles are combined, a cybrid results. Both are outcomes of chromosome elimination during culture.
Incorrect! Try again.
60Precursor 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.Lie on the biosynthetic pathway at a step that is rate-limiting or committed toward the target product
B.Be a final end-product that feedback-activates the pathway
C.Inhibit all competing branch pathways permanently
D.Be a primary metabolite unrelated to the target pathway
Correct Answer: Lie on the biosynthetic pathway at a step that is rate-limiting or committed toward the target product
Explanation:
Feeding a biosynthetic intermediate boosts yield only if it enters the pathway upstream of (or at) a limiting step and is channeled toward the desired product; feeding unrelated compounds or end-products does not increase flux to the target.
Incorrect! Try again.
Did this save you a night before the exam?
LPU Notes is free, and it stays free. Ads cover part of the server bill.
The rest comes out of a student's own pocket: the domain, the storage,
and keeping the site up through the weeks everyone needs it at once.
The payment button didn't load. An ad blocker or a filtered network is the usual reason.
to try again.
Nothing here is ever locked, and nothing unlocks. Chip in only if it was worth it.
What it pays for →