Revision: Biotechnology >> Biotechnology - Principles and Processes Biology Science (English Medium) Class 12 CBSE

The technique of bringing about improvements in living organisms by genetic modifications and hybridization, for the welfare of human beings is known as ‘Biotechnology’.

The European Federation of Biotechnology (EFB) defined biotechnology as ‘the integration of natural science and organisms, cells, parts thereof, and molecular analogues for products and services.’

• Biotechnology, a term coined by Karl Ereky in 1919, is the use of biological systems and genetic modifications to develop products and services for human welfare.
• Traditional biotechnology relies on small-scale, natural processes like fermentation (e.g., producing curd and wine), whereas modern biotechnology operates on a large scale.
• Modern biotechnology is fundamentally driven by two core techniques: genetic engineering (the targeted alteration of DNA and RNA) and bioprocess engineering.
• The field experienced a major breakthrough with the development of recombinant DNA technology by Cohen and Boyer in 1973.
• By integrating disciplines such as molecular biology and biochemistry, biotechnology enables crucial applications in both medicine (antibiotics, vaccines, insulin) and agriculture (high-yield, disease-resistant crops).

• Two Core Techniques - Modern biotechnology is based on (i) Genetic Engineering and (ii) Chemical Engineering.
• Genetic Engineering - Deals with the alteration of DNA and RNA to achieve desired results in a directed, predetermined way using in vitro processes.
• Chemical Engineering - Maintains a sterile environment for manufacturing useful products like vaccines, antibodies, enzymes, vitamins, and therapeutics.
• What Genetic Engineering Involves - Repairing/replacing defective genes, synthesising new genes, transferring genes, combining genes from two organisms, and altering genotype.
• Other Names for Genetic Engineering - Also called Recombinant DNA (rDNA) Technology or Gene Cloning, as it involves transferring a gene via a suitable vector to a new location or organism.

• Restriction enzymes, initially discovered as a bacterial defence mechanism, act as "molecular scissors" to cut DNA and are the fundamental tools of recombinant DNA technology.
• They belong to a class of enzymes called endonucleases, which cleave DNA at specific internal positions, unlike exonucleases that remove nucleotides from the ends.
• These enzymes recognise and bind to specific palindromic sequences, such as EcoRI's 5'-GAATTC-3', which read identically on both strands in the 5′ to 3′ direction.
• When cut at these sites, DNA produces either straight blunt ends or staggered sticky ends, which pair easily and are preferred for cloning.
• Restriction enzymes are named systematically after their bacterial source; for example, in EcoRI, 'E' is the genus, 'co' is the species, 'R' is the strain, and 'I' indicates the order of isolation.

• Vectors (like plasmids and bacteriophages) are DNA molecules used to carry and replicate foreign DNA inside a host cell.
• An ideal vector must have an origin of replication (ori), selectable markers, and specific cloning sites.
• pBR322 is a widely used standard bacterial plasmid vector containing these essential features.
• Recombinant DNA is identified using insertional inactivation (e.g., in blue-white selection, recombinant colonies appear white due to a disrupted gene).
• Higher organisms require specific vectors: Ti plasmids for plants and modified retroviruses for animals.

• DNA is hydrophilic, so it cannot enter cells easily; bacteria are made competent using Ca²⁺ ions.
• Cells are treated with cold (ice) and heat shock (42°C) to help the uptake of recombinant DNA.
• Transformation is the process of introducing recombinant DNA into bacterial cells.
• Microinjection → DNA is directly injected into the nucleus of animal cells.
• Biolistics (gene gun) and disarmed pathogens are used to transfer DNA into plant and host cells.

• Cells are first broken open using specific enzymes (such as lysozyme for bacteria) to successfully isolate the genetic material.
• The purified DNA is precisely cut at specific locations using restriction enzymes, which act as "molecular scissors" to extract the desired gene.
• The resulting DNA fragments are separated by size using gel electrophoresis, and the specific target sequence is extracted.
• The desired gene is then amplified into millions of copies using the Polymerase Chain Reaction (PCR) technique.
• The amplified gene is joined to a carrier vector using the enzyme DNA ligase to construct a new molecule called recombinant DNA.
• This recombinant DNA is introduced into a chemically treated, competent host cell (such as a bacterium) through a process known as transformation.
• For commercial use, these transformed host cells are cultured on a massive scale inside large, environmentally controlled vessels called bioreactors.
• The final therapeutic product undergoes downstream processing, which involves rigorous separation, purification, and quality testing before packaging.