Exploring the Fascinating World of Amino Acids in Biochemistry

biochemisty course no dtc 111 credit hours 2 1 1 n.w
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Dive into the realm of amino acids with this comprehensive guide covering their structure, classification, and unique properties. Understand the significance of essential amino acids, optical activity, zwitterions, and R-group classifications. Explore the diverse roles of amino acids in protein formation and their crucial importance in various biological processes. Join Associate Professor Binita Rani on an enlightening journey through the study of biochemistry and the fundamental building blocks of life.

  • Amino Acids
  • Biochemistry
  • Protein Formation
  • Essential Nutrients
  • Organic Chemistry

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  1. BIOCHEMISTY Course No.-DTC-111, Credit Hours 2 (1+1) AMINO ACIDS BINITA RANI ASSOCIATE PROFESSOR (DAIRY CHEMISTRY) FACULTY OF DAIRY TECHNOLOGY S.G.I.D.T., BVC CAMPUS, P.O.- BVC, DIST.-PATNA-800014

  2. Amino acid - both amino and carboxyl functional groups. H2NCHRCOOH - Alpha-amino acids carbon - to which the amino and carboxylate groups are attached Amino acids building blocks of proteins classified into essential and non-essential Twenty amino acids eight are essential . adequate consumption of amino acids : during development and maturation pregnancy, lactation, or injury (a burn, for instance). Complete protein source - all the essential amino acids Incomplete protein source - lacks one or more.

  3. Optical Property Protein - Twenty types of amino acids one- or three-letter abbreviations each amino acid representation in peptides. All amino acids have asymmetric carbon optically active, except glycine Amino acids can be dextrorotatory or levorotatory depending upon the rotation of plane polarized light L-amino acids represent majority of amino acids found in proteins. D-amino acids - produced by exotic sea-dwelling organisms L and D convention for amino acid configuration refers to optical activity of the glyceraldehyde isomer from which the amino acid is synthesized rather than the optical property of the acid itself (L-glyceraldehyde is levorotary; D- glyceraldehyde is dextrorotary)

  4. Non superimposable Mirror images of Amino Acids General structure of amino acid

  5. Zwitterions At isoelectric point, protonated ammonium groups and deprotonated carboxylate groups are equal, resulting net neutral charge and formation of Zwitterions Zwitterion can behave as both a base as well as an acid. For glycine, the isoelectric point is arithmetic mean of the two pKa values, because of absence of an ionizable group in its side chain. Glycine has a net negative charge at pH > pI. move towards the anode At pH < pI, glycine has a net positive charge move towards the cathode

  6. Classification of Amino acids As acidic, basic, aliphatic, aromatic, or sulfur-containing based on the R groups properties.

  7. Amino acids with aliphatic side chains

  8. Amino acids side chains with sulfur atoms

  9. Amino acids side chains with hydroxylic (OH) groups

  10. Amino acids with aromatic rings

  11. Amino acid side chain with basic group

  12. Amino acids side chains with acidic groups or their amides

  13. THANKS

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