Class XII Biology · Chapter 10

BIOTECHNOLOGY AND ITS APPLICATIONS

Master Biology · NEET quick revision

BIOTECHNOLOGY AND ITS APPLICATIONS

Complete NCERT Class 12 Chapter 5 comparison tables: nucleic acids, DNA packaging, gene expression, regulation and genome analysis.

8 essential comparison tables~10 min readLast position auto-saved
Biotechnology and Its Applications comparison tables
1. Tissue culture vs somatic hybridisation
In-vitro plant biotechnology
FeatureTissue cultureSomatic hybridisation
BasisWhole plant regenerated from an explant in sterile nutrient medium.Fusion of protoplasts from two different varieties/species.
Key propertyTotipotency - each plant cell/explant can generate a whole plant.Combines somatic cells after cell walls are removed.
ProductMicropropagation gives genetically identical somaclones.Somatic hybrid, e.g. pomato from tomato and potato protoplasts.
NCERT useMeristem culture produces virus-free plants.Creates novel hybrid combinations, though not all are commercially useful.
2. Conventional breeding vs genetically modified crops
Routes to crop improvement
FeatureConventional breedingGM crop approach
Gene transferTransfers many genes together through crossing.Introduces selected gene(s) through genetic manipulation.
Limitations / benefitsSlower and may bring undesirable genes.Can create pest resistance, stress tolerance and enhanced nutrient value.
ExamplesImproved varieties alongside agrochemical management.Golden rice, Bt cotton and tailor-made plants for starches, fuels or pharmaceuticals.
Environmental aimOften relies on fertilisers and pesticides.Can reduce pesticide reliance and improve mineral-use efficiency.
3. Bt protoxin vs activated Bt toxin
How Bt crops kill susceptible insects
FeatureBt protoxin in bacteriumActivated toxin in insect gut
StateInactive crystalline protein; does not harm the bacterium.Active form after alkaline pH solubilises and activates it.
TargetProduced by Bacillus thuringiensis.Binds midgut epithelial cells of susceptible larvae, creates pores and causes cell lysis.
Usecry genes are cloned into crop plants.Gives crop resistance to specific insect groups.
4. Important cry genes and target pests
NCERT Bt crop examples
Gene / proteinTargetKey point
cryIAc and cryIIAbCotton bollwormsGenes selected according to crop and target pest.
cryIAbCorn borerBt toxins are insect-group specific.
Bt cropsCotton, corn, rice, tomato, potato and soybeanExpress toxin gene and reduce insecticide requirement.
Other susceptible groupsLepidopterans, coleopterans and dipteransDifferent Bt strains produce proteins for different insects.
5. Sense RNA vs antisense RNA in RNA interference
RNAi-based nematode resistance
FeatureSense RNAAntisense RNA
RelationshipHas sequence corresponding to target mRNA.Complementary to sense RNA / target mRNA.
When both are producedThey form double-stranded RNA (dsRNA), which initiates RNA interference.
OutcomeSpecific mRNA is silenced, so translation does not occur. A tobacco plant expressing nematode-specific dsRNA resists Meloidogyne incognita.
6. Animal insulin vs recombinant human insulin
Insulin production for diabetes management
FeatureAnimal-source insulinRecombinant human insulin
SourcePancreas of slaughtered cattle or pigs.Human insulin DNA sequences expressed in E. coli.
ConcernCan cause allergy or immune reaction to foreign protein.Matches human insulin and avoids this non-human-source issue.
ProductionExtracted and purified from animals.Eli Lilly (1983) produced A and B chains separately, then joined them by disulphide bonds.
C-peptideHuman proinsulin contains it; mature insulin does not.Bacterial production bypassed the need to process a C-peptide by assembling separate chains.
7. Gene therapy vs enzyme replacement for ADA deficiency
Approaches to a hereditary immune disorder
FeatureGene therapyEnzyme replacement therapy
PrincipleIntroduces normal functional ADA gene to compensate for deleted/non-functional gene.Provides functional ADA enzyme by injection.
Procedure in NCERT examplePatient lymphocytes are cultured, given ADA cDNA with retroviral vector and returned.Repeated administration of enzyme.
Limitation / potentialLymphocytes are not immortal, so periodic infusion is needed; early embryonic delivery may be permanent.Not completely curative and requires repeated treatment.
8. PCR vs ELISA vs DNA/RNA probe
Early molecular diagnosis
TechniqueWhat it detectsPrinciple / example
PCRVery low amount of pathogen DNA/RNA or mutation.Amplifies nucleic acid; used for HIV detection and suspected cancer mutations.
ELISAPathogen antigen or antibodies made against pathogen.Based on antigen-antibody interaction.
Probe hybridisationSpecific normal or mutated DNA sequence.Radioactively labelled single-stranded DNA/RNA hybridises with complementary sequence; detected by autoradiography.
9. Uses of transgenic animals
Why animals carrying foreign genes are made
UsePurpose / example
Normal physiology and developmentStudies gene regulation and roles in normal growth and development.
Disease modelsModels of cancer, cystic fibrosis, rheumatoid arthritis and Alzheimer's disease test treatments.
Biological productsHuman alpha-1-antitrypsin for emphysema; transgenic cow Rosie produced human alpha-lactalbumin-enriched milk.
Vaccine and chemical safetyTransgenic mice test polio-vaccine safety; sensitive animals speed toxicity testing.
10. Biosafety regulation vs biopiracy
Ethical issues in biotechnology
FeatureBiosafety regulationBiopiracy
ConcernUnpredictable ecosystem effects and safety of GM research/organisms.Unauthorised use of bio-resources or traditional knowledge without compensation.
Indian exampleGEAC evaluates validity of GM research and safety for public use.Patent claims relating to Basmati, turmeric and neem raise benefit-sharing concerns.
PurposeResponsible, regulated use of genetic modification.Protects biodiversity-rich communities and countries from unfair commercial exploitation.