Biotechnology: Principles and Processes Part-5

Polymerase Chain Reaction

graph TB PCR(Polymerase Chain Reaction) PCR --> DNA[DNA Denaturation] PCR --> Primer[Primer Annealing] PCR --> Extension[Extension/elongation] DNA --> T1[Temperature: 94-98°C] Primer --> T2[Temperature: 50-65°C] Extension --> T3[Temperature: 72°C] T1 --> T1a[Breaks hydrogen bonds] T2 --> T2a[Primers bind to target DNA] T3 --> T3a[DNA polymerase synthesizes new DNA]

DNA

graph TD; DNA{{DNA}} DNA --> Nucleotides{{Nucleotides}} DNA --> DoubleHelix{{Double Helix}} DNA --> Replication{{Replication}} Nucleotides --> Adenine{{Adenine}} Nucleotides --> Thymine{{Thymine}} Nucleotides --> Cytosine{{Cytosine}} Nucleotides --> Guanine{{Guanine}} DoubleHelix --> BasePairing{{Base Pairing}} Replication --> SemiConservative{{Semi Conservative}} Replication --> Enzymes{{Enzymes involved in DNA replication}}

DNA Synthesis

graph TB A[DNA Synthesis] A --> B[DNA Replication] B --> C[Helicase] B --> D[DNA Polymerase] B --> E[Primase] A --> F[DNA Repair] F --> G[DNA Ligase] F --> H[Exonuclease] F --> I[Endonuclease] A --> J[DNA Recombination] J --> K[Homologous Recombination] J --> L[Site-specific Recombination] J --> M[Transposition]

Recuirments for PCR

graph TD; PCR[Requirements for PCR]; PCR --> Primer[Primers]; PCR --> dNTPs[dNTPs]; PCR --> Buffer[Buffer]; PCR --> Taq[Taq Polymerase]; PCR --> Template[Template DNA]; PCR --> Machine[PCR Machine]; Primer --> Forward[Forward Primer]; Primer --> Reverse[Reverse Primer]; dNTPs --> Adenine[A]; dNTPs --> Thymine[T]; dNTPs --> Cytosine[C]; dNTPs --> Guanine[G]; Buffer --> pH[pH]; Buffer --> Mg[Mg++]; Taq --> Heat[Heat Resistance]; Template --> Source[Source of DNA]; Machine --> Cycles[Cycling Conditions];

Polymerase Chain Reaction Stages

graph TD; PCR["Polymerase Chain Reaction Stages"]; PCR --> Denaturation; PCR --> Annealing; PCR --> Extension; Denaturation["1. Denaturation: DNA strands separate"]; Annealing["2. Annealing: Primers bind to the DNA"]; Extension["3. Extension: New DNA is made by the Taq polymerase"];

Instrumentation: Thermal cycler

graph TD; A[Instrumentation: Thermal cycler]; B[Definition]; C[Uses]; D[Types]; E[Components]; F[Working Principle]; G[Applications in Biology]; A-->B; A-->C; A-->D; A-->E; A-->F; A-->G;

Analysis of PCR Reaction

graph TD; A[Analysis of PCR Reaction]; B[PCR Basics]; C[PCR Components]; D[PCR Steps]; E[PCR Variations]; F[PCR Applications]; G[PCR Limitations]; A-->B; A-->C; A-->D; A-->E; A-->F; A-->G; B-->H{DNA}; B-->I{Primers}; C-->J{DNA Polymerase}; C-->K{dNTPs}; C-->L{Buffer}; D-->M[Denaturation]; D-->N[Annealing]; D-->O[Extension]; E-->P[Real-time PCR]; E-->Q[Reverse transcription PCR]; E-->R[Digital PCR]; F-->S[Genetic Testing]; F-->T[Forensics]; F-->U[Research]; G-->V[Errors]; G-->W[Sensitivity]; G-->X[Specificity];

Restriction Digestion and Ligation

graph TB A[Restriction Digestion and Ligation] A --> B[Restriction Digestion] B --> C[Definition] B --> D[Process] B --> E[Applications] A --> F[Ligation] F --> G[Definition] F --> H[Process] F --> I[Applications]


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