This document discusses nucleotides, nucleosides, nucleic acids, and their structures and functions. Some key points:
- Nucleotides are composed of a nitrogenous base, sugar (ribose or deoxyribose), and phosphate. Nucleosides lack the phosphate.
- Purine nucleosides contain adenine or guanine, while pyrimidine nucleosides contain cytosine, uracil, or thymine.
- Nucleotides and nucleosides play important roles in cell signaling, energy storage, and as components of nucleic acids and coenzymes.
- Nucleic acids DNA and RNA are polymers of nucleotides. DNA has the sugar deoxyrib
This document discusses nucleotide chemistry. Nucleotides are organic compounds composed of a phosphate group, nitrogenous base, and a sugar molecule. They serve as the building blocks of nucleic acids DNA and RNA. Nucleotides also function as sources of chemical energy through molecules like ATP and GTP, and participate in cellular signaling through molecules like cAMP and cGMP. The document goes on to describe the specific sugars, bases, nucleosides, and nucleotides that make up DNA and RNA. It provides details on nucleotide nomenclature and classification and discusses important adenosine-containing nucleotides and their roles, such as ATP serving as an important energy source in many cellular processes.
This document summarizes the process of de novo fatty acid synthesis. It occurs in the cytosol of liver, kidney, adipose tissue, and lactating mammary glands. Acetyl-CoA is the starting material, which is transported from mitochondria to the cytosol via citrate. In the cytosol, fatty acid synthase complex catalyzes the reactions to produce palmitic acid (C16) through cycles of condensation, reduction, dehydration, and reduction. The process requires acetyl-CoA, malonyl-CoA, ATP, and NADPH as substrates and is regulated by enzymes and hormones.
Nucleic acids are polymers of nucleotides linked by phosphodiester bonds. There are two types: DNA and RNA. DNA contains the genetic information and directs protein synthesis. It exists as a double helix with nucleotides paired through hydrogen bonds between complementary bases (A-T and G-C). RNA is single-stranded and also involved in protein synthesis.
The document discusses the structure and functions of nucleic acids and proteins. It describes the four levels of structure for both - primary, secondary, tertiary, and quaternary. For nucleic acids, this includes the nucleotide components, base pairing, and interactions with other molecules. For proteins, it includes the amino acid sequence, folding patterns like alpha helices and beta sheets, and bonding interactions that give shape. Nucleic acids function to store and transmit genetic information and direct protein synthesis. Proteins function in roles like repair, energy, movement, catalysis, transport, and structure.
Biochem nucleotides(structure and functions) june.18.2010MBBS IMS MSU
Nucleic acids are made up of monomeric units called nucleotides. Nucleotides serve important biochemical functions as components of coenzymes involved in transferring phosphoryl, sugar, lipid groups. They also function as second messengers like cAMP and cGMP. Synthetic nucleotides containing halogens or additional nitrogen are used in chemotherapy and immunosuppression. Purines and pyrimidines are heterocyclic nitrogen-containing compounds that form the bases of nucleic acids. Nucleosides are derivatives of bases linked to a sugar, while nucleotides contain a phosphoryl group attached to the sugar. RNA and DNA are made up of ribonucleotides and deoxyribonucleotides formed through a series of phosphorylation and conversion reactions in
Pyrimidine nucleotides are catabolized into highly water soluble compounds unlike purines. The end products of pyrimidine metabolism are carbon dioxide, ammonia, beta-alanine, and beta-aminoisobutyrate. Beta-aminoisobutyrate is transaminated into other compounds that can enter the citric acid cycle or be used for fatty acid synthesis.
The document summarizes the de novo synthesis of pyrimidine nucleotides in three steps. First, carbamoyl phosphate and aspartate condense to form carbamoyl aspartate. Second, the pyrimidine ring forms and is further modified through a series of reactions to eventually form orotidine monophosphate. Third, OMP undergoes reactions to form the pyrimidine nucleotides UMP, UDP, UTP, CTP, and through additional steps, dUMP and dTMP. Key enzymes involved include carbamoyl phosphate synthetase, aspartate transcarbamoylase, and OMP decarboxylase. Feedback inhibition regulates the process.
Gives in detail primary, secondary, tertiary and Quaternary structure of proteins. Gives classification of secondary structure: alpha helix, beta pleated sheet and different types of tight turns and explains most commonly found tight turn in proteins i.e. beta turn. Briefs about the Ramachandran plot of proteins, dihedral or torsion angles and explains why glycine and proline act as alpha helix breakers. Explains tertiary structure of proteins and different covalent and non covalent bonds in the tertiary structure and relative importance of these bonding interactions. Details about the quaternary structure of proteins and explains why hemoglobin is a quaternary protein and insulin is not.
This document discusses nucleotide chemistry. Nucleotides are organic compounds composed of a phosphate group, nitrogenous base, and a sugar molecule. They serve as the building blocks of nucleic acids DNA and RNA. Nucleotides also function as sources of chemical energy through molecules like ATP and GTP, and participate in cellular signaling through molecules like cAMP and cGMP. The document goes on to describe the specific sugars, bases, nucleosides, and nucleotides that make up DNA and RNA. It provides details on nucleotide nomenclature and classification and discusses important adenosine-containing nucleotides and their roles, such as ATP serving as an important energy source in many cellular processes.
This document summarizes the process of de novo fatty acid synthesis. It occurs in the cytosol of liver, kidney, adipose tissue, and lactating mammary glands. Acetyl-CoA is the starting material, which is transported from mitochondria to the cytosol via citrate. In the cytosol, fatty acid synthase complex catalyzes the reactions to produce palmitic acid (C16) through cycles of condensation, reduction, dehydration, and reduction. The process requires acetyl-CoA, malonyl-CoA, ATP, and NADPH as substrates and is regulated by enzymes and hormones.
Nucleic acids are polymers of nucleotides linked by phosphodiester bonds. There are two types: DNA and RNA. DNA contains the genetic information and directs protein synthesis. It exists as a double helix with nucleotides paired through hydrogen bonds between complementary bases (A-T and G-C). RNA is single-stranded and also involved in protein synthesis.
The document discusses the structure and functions of nucleic acids and proteins. It describes the four levels of structure for both - primary, secondary, tertiary, and quaternary. For nucleic acids, this includes the nucleotide components, base pairing, and interactions with other molecules. For proteins, it includes the amino acid sequence, folding patterns like alpha helices and beta sheets, and bonding interactions that give shape. Nucleic acids function to store and transmit genetic information and direct protein synthesis. Proteins function in roles like repair, energy, movement, catalysis, transport, and structure.
Biochem nucleotides(structure and functions) june.18.2010MBBS IMS MSU
Nucleic acids are made up of monomeric units called nucleotides. Nucleotides serve important biochemical functions as components of coenzymes involved in transferring phosphoryl, sugar, lipid groups. They also function as second messengers like cAMP and cGMP. Synthetic nucleotides containing halogens or additional nitrogen are used in chemotherapy and immunosuppression. Purines and pyrimidines are heterocyclic nitrogen-containing compounds that form the bases of nucleic acids. Nucleosides are derivatives of bases linked to a sugar, while nucleotides contain a phosphoryl group attached to the sugar. RNA and DNA are made up of ribonucleotides and deoxyribonucleotides formed through a series of phosphorylation and conversion reactions in
Pyrimidine nucleotides are catabolized into highly water soluble compounds unlike purines. The end products of pyrimidine metabolism are carbon dioxide, ammonia, beta-alanine, and beta-aminoisobutyrate. Beta-aminoisobutyrate is transaminated into other compounds that can enter the citric acid cycle or be used for fatty acid synthesis.
The document summarizes the de novo synthesis of pyrimidine nucleotides in three steps. First, carbamoyl phosphate and aspartate condense to form carbamoyl aspartate. Second, the pyrimidine ring forms and is further modified through a series of reactions to eventually form orotidine monophosphate. Third, OMP undergoes reactions to form the pyrimidine nucleotides UMP, UDP, UTP, CTP, and through additional steps, dUMP and dTMP. Key enzymes involved include carbamoyl phosphate synthetase, aspartate transcarbamoylase, and OMP decarboxylase. Feedback inhibition regulates the process.
Gives in detail primary, secondary, tertiary and Quaternary structure of proteins. Gives classification of secondary structure: alpha helix, beta pleated sheet and different types of tight turns and explains most commonly found tight turn in proteins i.e. beta turn. Briefs about the Ramachandran plot of proteins, dihedral or torsion angles and explains why glycine and proline act as alpha helix breakers. Explains tertiary structure of proteins and different covalent and non covalent bonds in the tertiary structure and relative importance of these bonding interactions. Details about the quaternary structure of proteins and explains why hemoglobin is a quaternary protein and insulin is not.
5 nucleotides and nucleic acids lectureSiham Gritly
This document discusses nucleotides, nucleic acids, and their roles in biology. It describes how nucleotides are composed of a nitrogenous base bonded to a pentose sugar and phosphate group. Nucleotides bond together via phosphodiester bonds to form nucleic acids like DNA and RNA, which store and transmit genetic information in living cells. The document outlines the structures of nucleotides and nucleic acids and differentiates between ribonucleotides and deoxyribonucleotides.
DNA and RNA molecules are linear polymers built from individual units called nucleotides connected by bonds called phosphodiester linkages. DNA and RNA are used to store and pass genetic information from one generation to the next.
Nucleotide metabolism (purine and pyrimidine synthesis)Areeba Ghayas
NUCLEOTIDE METABOLISM,DE NOVO SYNTHESIS OF PURINE, SALVAGE PATHWAY OF PURINE, DE-NOVO SYNTHESIS OF PYRIMIDINE, SALVAGE PATHWAY OF PYRIMIDINE, GOUT, HYPERURICEMIA, LESCH-NYAN SYNDROME, OROTIC ACIDURIA
- Nucleotides are composed of a nitrogenous base (purine or pyrimidine), a pentose sugar (ribose or deoxyribose), and one or more phosphate groups. When a base combines with a sugar, a nucleoside is formed. The addition of phosphate groups forms nucleotides.
- The four bases found in nucleic acids are adenine, guanine, cytosine, and either thymine in DNA or uracil in RNA. These bases combine with either ribose or deoxyribose to form nucleosides like AMP, GMP, CMP, TMP, or UMP.
- Nucleotides are the monomers that make up nucleic acids DNA and RNA
This document discusses biological oxidation and the thermodynamic principles involved. It describes the key variables of enthalpy, entropy and free energy. Biological oxidation involves the transfer of electrons through redox couples and redox potential is a quantitative measure of electron transfer tendency. ATP is an important energy currency produced through substrate-level phosphorylation and oxidative phosphorylation, where electrons are transferred through the electron transport chain and energy is trapped as ATP.
This document provides an overview of nucleotide biosynthesis. It discusses that nucleotides are composed of nitrogenous bases, pentose sugars, and phosphate groups, and are the building blocks of nucleic acids. There are two pathways for nucleotide biosynthesis - de novo synthesis which uses metabolic precursors to build nucleotides from scratch, and salvage pathways which recycle bases and nucleosides from nucleic acid breakdown. Key steps in purine and pyrimidine synthesis are described. Nucleotides have important biological functions as components of nucleic acids, energy carriers, and signaling molecules.
Nucleic acids like DNA and RNA are composed of nucleotides, which contain a nitrogenous base (purine or pyrimidine), a 5-carbon sugar (ribose or deoxyribose), and one or more phosphate groups. Friedrich Miescher first isolated nucleic acids in 1869. DNA exists as a double-stranded helical structure, with the bases on one strand bonding with complementary bases on the other strand. The sugar-phosphate backbone of DNA contains alternating sugar and phosphate groups and runs in the same direction on both strands.
This document discusses nucleotides, their synthesis and degradation. It covers the following key points:
1. Nucleotides are composed of a nucleoside (a nitrogenous base linked to a 5-carbon sugar) bound to one or more phosphate groups. They are the monomers that make up nucleic acids like RNA and DNA.
2. Purine nucleotides are synthesized de novo through a complex 10 step pathway beginning with phosphoribosyl pyrophosphate (PRPP) and ending with inosine monophosphate (IMP). Pyrimidine nucleotides can also be synthesized from PRPP.
3. Nucleotides can be broken down through both intracellular catabolism pathways that generate purine
RNA is one of the major biological macromolecules essential for life. It has several types that serve different functions. Messenger RNA (mRNA) carries genetic information from DNA to the ribosomes for protein synthesis. Ribosomal RNA (rRNA) is the catalytic component of ribosomes and is involved in protein translation. Transfer RNA (tRNA) transfers specific amino acids to the growing polypeptide chain during translation.
Enzymes are usually proteins that act as catalysts and speed up biochemical reactions without being consumed. They have optimal temperatures and pH levels for activity. The Michaelis-Menten equation describes how reaction velocity varies with substrate concentration. Competitive inhibitors bind the enzyme's active site, increasing Km; noncompetitive inhibitors bind elsewhere, decreasing Vmax. Enzymes are important clinically as markers of tissue damage - creatine kinase and lactate dehydrogenase indicate heart attacks, while alanine transaminase, aspartate transaminase and alkaline phosphatase detect liver disease. Troponin is a very specific marker for myocardial infarction.
Pyruvate is converted to acetyl CoA by the pyruvate dehydrogenase (PDH) complex in the mitochondria. PDH is a multi-enzyme complex containing five coenzymes and three enzymes that catalyzes the oxidative decarboxylation of pyruvate. This generates acetyl CoA, NADH, and FADH2, with the NADH and FADH2 contributing to ATP production through oxidative phosphorylation. PDH activity is regulated by phosphorylation/dephosphorylation and end-product inhibition by acetyl CoA and NADH.
The document discusses fatty acid synthesis. It begins by describing fatty acids and their roles in the body. It then covers the three main ways fatty acids are produced: diet, adipolysis, and de novo synthesis. The process of de novo synthesis occurs primarily in the liver, adipose tissue, and lactating mammary glands. It involves acetyl-CoA being carboxylated to malonyl-CoA by acetyl-CoA carboxylase. Fatty acid synthase then catalyzes the repeating cycles of condensation, reduction, dehydration, and reduction to elongate the fatty acid chain until a 16-carbon palmitate is produced. NADPH provides reducing equivalents for the reactions.
The slide has some brief introduction to nucleotide chemistry, History, General features of nucleotides, Nomenclature, Individual properties of bases, Classification
and Synthetic analogues of biomedical importance.
The pentose phosphate pathway generates NADPH and pentose sugars. It has both an oxidative and non-oxidative phase. In the oxidative phase, glucose-6-phosphate is oxidized to produce NADPH. In the non-oxidative phase, 5-carbon sugars are converted into 3 and 6 carbon sugars through a series of isomerization, epimerization, and transketolase reactions. The pathway is important as it provides NADPH for biosynthetic reactions and pentose sugars for nucleotide synthesis. A defect in glucose-6-phosphate dehydrogenase can lead to insufficient NADPH and glutathione, resulting in hemolytic anemia due to oxidative damage of red blood cells.
ATP synthase—also called FoF1 ATPase is the universal protein that terminates oxidative phosphorylation by synthesizing ATP from ADP and phosphate.
ATP Synthase is one of the most important enzymes found in the mitochondria of cells
Synthesis of purines and pyrimidines, De novo synthesis of purines, De novo synthesis of pyrimidines, salvage synthesis of purines, salvage synthesis of pyrimidines
This document discusses the degradation of nucleic acids. It notes that nucleotides are the building blocks of nucleic acids and can be either RNA nucleotides or DNA nucleotides. The nucleotides are further broken down into purine nucleotides and pyrimidine nucleotides. It then describes the specific degradation pathways for purine nucleotides and pyrimidine nucleotides. For purines, the end product is uric acid, while pyrimidines lead to ammonia and urea production. It also discusses some related medical conditions like gout that can result from problems in nucleic acid degradation.
This document summarizes the de novo synthesis of fatty acids. It discusses that fatty acid synthesis primarily occurs in the liver and lactating mammary glands using acetyl CoA, ATP, NADPH, Mn2+, and biotin. The first step is the production of cytosolic acetyl CoA from mitochondrial acetyl CoA. Acetyl CoA is then carboxylated to form malonyl CoA by acetyl CoA carboxylase. Fatty acid synthase is a multifunctional enzyme that catalyzes the remaining reactions. The major sources of NADPH required are the pentose phosphate pathway and conversion of malate to pyruvate in the cytosol. Palmitate, a 16 carbon
introduction of Purine and Pyrimidine metabolism, biosynthesis and degradation of nucleotides, biological functions and metabolic disorders, chemical analogues and therapeutic drugs, uric acid metabolism
1. Nucleic acids consist of nitrogen bases, pentose sugars, and phosphates. The pentose sugar is D-ribose in RNA and 2-deoxy D-ribose in DNA.
2. Purine nucleotides are synthesized through a de novo pathway where inosine monophosphate (IMP) is synthesized from basic building blocks like aspartate, glycine, and glutamine and later converted to AMP and GMP.
3. Pyrimidine nucleotides are synthesized by first forming orotidine monophosphate from aspartate, carbamoyl phosphate, and glutamine, which is then converted to UMP and other pyrimidine nucleotides.
Biochemistry of nucleic acids DNA RNA structures with the comparison chart between them chemistry of nucleic acids structures and composition and protein synthesis nucleotides and nucleosides
The document discusses nucleotides, which are the basic units of nucleic acids. Nucleotides consist of a nitrogen base, a pentose sugar (either ribose or deoxyribose), and one or more phosphate groups. There are two types of nitrogen bases - purines and pyrimidines. Nucleotides can combine to form nucleic acids like DNA and RNA, which carry the genetic information in cells and direct protein synthesis. DNA has the sugar deoxyribose and the bases adenine, guanine, cytosine, and thymine. RNA contains the sugar ribose and replaces thymine with uracil. Nucleotides and nucleic acids play crucial roles in storing and transmitting genetic information in living organisms.
5 nucleotides and nucleic acids lectureSiham Gritly
This document discusses nucleotides, nucleic acids, and their roles in biology. It describes how nucleotides are composed of a nitrogenous base bonded to a pentose sugar and phosphate group. Nucleotides bond together via phosphodiester bonds to form nucleic acids like DNA and RNA, which store and transmit genetic information in living cells. The document outlines the structures of nucleotides and nucleic acids and differentiates between ribonucleotides and deoxyribonucleotides.
DNA and RNA molecules are linear polymers built from individual units called nucleotides connected by bonds called phosphodiester linkages. DNA and RNA are used to store and pass genetic information from one generation to the next.
Nucleotide metabolism (purine and pyrimidine synthesis)Areeba Ghayas
NUCLEOTIDE METABOLISM,DE NOVO SYNTHESIS OF PURINE, SALVAGE PATHWAY OF PURINE, DE-NOVO SYNTHESIS OF PYRIMIDINE, SALVAGE PATHWAY OF PYRIMIDINE, GOUT, HYPERURICEMIA, LESCH-NYAN SYNDROME, OROTIC ACIDURIA
- Nucleotides are composed of a nitrogenous base (purine or pyrimidine), a pentose sugar (ribose or deoxyribose), and one or more phosphate groups. When a base combines with a sugar, a nucleoside is formed. The addition of phosphate groups forms nucleotides.
- The four bases found in nucleic acids are adenine, guanine, cytosine, and either thymine in DNA or uracil in RNA. These bases combine with either ribose or deoxyribose to form nucleosides like AMP, GMP, CMP, TMP, or UMP.
- Nucleotides are the monomers that make up nucleic acids DNA and RNA
This document discusses biological oxidation and the thermodynamic principles involved. It describes the key variables of enthalpy, entropy and free energy. Biological oxidation involves the transfer of electrons through redox couples and redox potential is a quantitative measure of electron transfer tendency. ATP is an important energy currency produced through substrate-level phosphorylation and oxidative phosphorylation, where electrons are transferred through the electron transport chain and energy is trapped as ATP.
This document provides an overview of nucleotide biosynthesis. It discusses that nucleotides are composed of nitrogenous bases, pentose sugars, and phosphate groups, and are the building blocks of nucleic acids. There are two pathways for nucleotide biosynthesis - de novo synthesis which uses metabolic precursors to build nucleotides from scratch, and salvage pathways which recycle bases and nucleosides from nucleic acid breakdown. Key steps in purine and pyrimidine synthesis are described. Nucleotides have important biological functions as components of nucleic acids, energy carriers, and signaling molecules.
Nucleic acids like DNA and RNA are composed of nucleotides, which contain a nitrogenous base (purine or pyrimidine), a 5-carbon sugar (ribose or deoxyribose), and one or more phosphate groups. Friedrich Miescher first isolated nucleic acids in 1869. DNA exists as a double-stranded helical structure, with the bases on one strand bonding with complementary bases on the other strand. The sugar-phosphate backbone of DNA contains alternating sugar and phosphate groups and runs in the same direction on both strands.
This document discusses nucleotides, their synthesis and degradation. It covers the following key points:
1. Nucleotides are composed of a nucleoside (a nitrogenous base linked to a 5-carbon sugar) bound to one or more phosphate groups. They are the monomers that make up nucleic acids like RNA and DNA.
2. Purine nucleotides are synthesized de novo through a complex 10 step pathway beginning with phosphoribosyl pyrophosphate (PRPP) and ending with inosine monophosphate (IMP). Pyrimidine nucleotides can also be synthesized from PRPP.
3. Nucleotides can be broken down through both intracellular catabolism pathways that generate purine
RNA is one of the major biological macromolecules essential for life. It has several types that serve different functions. Messenger RNA (mRNA) carries genetic information from DNA to the ribosomes for protein synthesis. Ribosomal RNA (rRNA) is the catalytic component of ribosomes and is involved in protein translation. Transfer RNA (tRNA) transfers specific amino acids to the growing polypeptide chain during translation.
Enzymes are usually proteins that act as catalysts and speed up biochemical reactions without being consumed. They have optimal temperatures and pH levels for activity. The Michaelis-Menten equation describes how reaction velocity varies with substrate concentration. Competitive inhibitors bind the enzyme's active site, increasing Km; noncompetitive inhibitors bind elsewhere, decreasing Vmax. Enzymes are important clinically as markers of tissue damage - creatine kinase and lactate dehydrogenase indicate heart attacks, while alanine transaminase, aspartate transaminase and alkaline phosphatase detect liver disease. Troponin is a very specific marker for myocardial infarction.
Pyruvate is converted to acetyl CoA by the pyruvate dehydrogenase (PDH) complex in the mitochondria. PDH is a multi-enzyme complex containing five coenzymes and three enzymes that catalyzes the oxidative decarboxylation of pyruvate. This generates acetyl CoA, NADH, and FADH2, with the NADH and FADH2 contributing to ATP production through oxidative phosphorylation. PDH activity is regulated by phosphorylation/dephosphorylation and end-product inhibition by acetyl CoA and NADH.
The document discusses fatty acid synthesis. It begins by describing fatty acids and their roles in the body. It then covers the three main ways fatty acids are produced: diet, adipolysis, and de novo synthesis. The process of de novo synthesis occurs primarily in the liver, adipose tissue, and lactating mammary glands. It involves acetyl-CoA being carboxylated to malonyl-CoA by acetyl-CoA carboxylase. Fatty acid synthase then catalyzes the repeating cycles of condensation, reduction, dehydration, and reduction to elongate the fatty acid chain until a 16-carbon palmitate is produced. NADPH provides reducing equivalents for the reactions.
The slide has some brief introduction to nucleotide chemistry, History, General features of nucleotides, Nomenclature, Individual properties of bases, Classification
and Synthetic analogues of biomedical importance.
The pentose phosphate pathway generates NADPH and pentose sugars. It has both an oxidative and non-oxidative phase. In the oxidative phase, glucose-6-phosphate is oxidized to produce NADPH. In the non-oxidative phase, 5-carbon sugars are converted into 3 and 6 carbon sugars through a series of isomerization, epimerization, and transketolase reactions. The pathway is important as it provides NADPH for biosynthetic reactions and pentose sugars for nucleotide synthesis. A defect in glucose-6-phosphate dehydrogenase can lead to insufficient NADPH and glutathione, resulting in hemolytic anemia due to oxidative damage of red blood cells.
ATP synthase—also called FoF1 ATPase is the universal protein that terminates oxidative phosphorylation by synthesizing ATP from ADP and phosphate.
ATP Synthase is one of the most important enzymes found in the mitochondria of cells
Synthesis of purines and pyrimidines, De novo synthesis of purines, De novo synthesis of pyrimidines, salvage synthesis of purines, salvage synthesis of pyrimidines
This document discusses the degradation of nucleic acids. It notes that nucleotides are the building blocks of nucleic acids and can be either RNA nucleotides or DNA nucleotides. The nucleotides are further broken down into purine nucleotides and pyrimidine nucleotides. It then describes the specific degradation pathways for purine nucleotides and pyrimidine nucleotides. For purines, the end product is uric acid, while pyrimidines lead to ammonia and urea production. It also discusses some related medical conditions like gout that can result from problems in nucleic acid degradation.
This document summarizes the de novo synthesis of fatty acids. It discusses that fatty acid synthesis primarily occurs in the liver and lactating mammary glands using acetyl CoA, ATP, NADPH, Mn2+, and biotin. The first step is the production of cytosolic acetyl CoA from mitochondrial acetyl CoA. Acetyl CoA is then carboxylated to form malonyl CoA by acetyl CoA carboxylase. Fatty acid synthase is a multifunctional enzyme that catalyzes the remaining reactions. The major sources of NADPH required are the pentose phosphate pathway and conversion of malate to pyruvate in the cytosol. Palmitate, a 16 carbon
introduction of Purine and Pyrimidine metabolism, biosynthesis and degradation of nucleotides, biological functions and metabolic disorders, chemical analogues and therapeutic drugs, uric acid metabolism
1. Nucleic acids consist of nitrogen bases, pentose sugars, and phosphates. The pentose sugar is D-ribose in RNA and 2-deoxy D-ribose in DNA.
2. Purine nucleotides are synthesized through a de novo pathway where inosine monophosphate (IMP) is synthesized from basic building blocks like aspartate, glycine, and glutamine and later converted to AMP and GMP.
3. Pyrimidine nucleotides are synthesized by first forming orotidine monophosphate from aspartate, carbamoyl phosphate, and glutamine, which is then converted to UMP and other pyrimidine nucleotides.
Biochemistry of nucleic acids DNA RNA structures with the comparison chart between them chemistry of nucleic acids structures and composition and protein synthesis nucleotides and nucleosides
The document discusses nucleotides, which are the basic units of nucleic acids. Nucleotides consist of a nitrogen base, a pentose sugar (either ribose or deoxyribose), and one or more phosphate groups. There are two types of nitrogen bases - purines and pyrimidines. Nucleotides can combine to form nucleic acids like DNA and RNA, which carry the genetic information in cells and direct protein synthesis. DNA has the sugar deoxyribose and the bases adenine, guanine, cytosine, and thymine. RNA contains the sugar ribose and replaces thymine with uracil. Nucleotides and nucleic acids play crucial roles in storing and transmitting genetic information in living organisms.
Nuclei acid is a naturally occurring chemical compound containing phosphoric acid, sugars, and a mixture of organic bases (purines and pyrimidines).
The two main classes of nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
DNA is the master blueprint for life and constitutes the genetic material in all free-living organisms and most viruses. DNA is the chemical basis of heredity and may be regarded as the reserve bank of genetic formation. DNA is exclusively responsible for maintaining the identity of different species of organisms over millions of years.
RNA is the genetic material of certain viruses, but it is also found in all living cells. The genes control protein synthesis through the mediation of RNA.
Nucleotides are the basic building blocks of nucleic acids DNA and RNA. They consist of a nitrogenous base, a pentose sugar and phosphate groups. Nucleotides combine to form nucleic acids and act as carriers of genetic information and cellular energy. Some synthetic nucleotide analogs are used as chemotherapy drugs by incorporating into DNA and disrupting nucleic acid synthesis. Nucleic acids DNA and RNA store and transmit genetic information through their linear polymers of nucleotides joined by phosphodiester bonds into strands with distinct primary, secondary and tertiary structures.
Nucleotides are the basic building blocks of nucleic acids DNA and RNA. They consist of a nitrogenous base, a pentose sugar and phosphate groups. Nucleotides combine to form nucleic acids and act as carriers of genetic information and cellular energy. Some synthetic nucleotide analogs are used as chemotherapy drugs by incorporating into DNA and disrupting nucleic acid synthesis. Nucleic acids DNA and RNA store and transmit genetic information through their linear polymers of nucleotides joined by phosphodiester bonds into strands with distinct primary, secondary and tertiary structures.
Types of nucliec acids, biosynthesis and catabolismShereen
1. The document discusses nucleic acids, their biosynthesis, and catabolism. It describes the two main types of nucleic acids - DNA and RNA, how they are synthesized through de novo and salvage pathways, and their components.
2. It provides details on the structures of DNA and RNA, including their nitrogenous bases, pentose sugars, and phosphate groups. DNA is double-stranded and found in the nucleus, while RNA exists in several forms and has roles in protein synthesis.
3. Nucleic acid catabolism and the roles of the different RNA types - mRNA, tRNA, and rRNA - in gene expression and protein synthesis are also summarized.
Molecular biology is the study of biological phenomena at the molecular level, particularly proteins, nucleic acids, and enzymes. In the early 1950s, knowledge of protein structure enabled the description of DNA structure as a double helix. The discovery of restriction enzymes in the 1970s allowed for recombinant DNA technology, which molecular biologists use to isolate and modify genes. DNA is made up of nucleotides containing nitrogenous bases and a sugar-phosphate backbone. The four bases in DNA—adenine, guanine, cytosine, and thymine—bind together in base pairs across the double helix in a complementary manner.
This document discusses nucleotides, their chemistry and metabolism. It covers the following key points:
- Nucleotides are composed of a nitrogenous base, a pentose sugar (ribose or deoxyribose), and phosphate groups. They are precursors to nucleic acids DNA and RNA.
- Purines and pyrimidines are the nitrogenous bases present in nucleotides. Adenine, guanine, cytosine and thymine are the major bases.
- Nucleotides are synthesized through two pathways - de novo synthesis which builds purine rings from simple precursors, and the salvage pathway which recycles purines.
- The major sites of purine synthesis are the liver and degradation
Nucleic acids are polymeric macromolecules essential for life. They include DNA and RNA and are made of nucleotides. DNA contains the genetic instructions in cells and is organized into chromosomes. It exists as a double helix held together by base pairing between purines and pyrimidines. RNA has several types and functions in protein synthesis or regulation. Nucleotides are the monomers of nucleic acids and also have important roles in metabolism. DNA is tightly packaged in the nucleus through winding around histone proteins to form nucleosomes and higher-order chromatin structures.
This document discusses nucleotides, nucleic acids, DNA and RNA. It begins by explaining that nucleic acids are made up of nucleotides, and the two main nucleic acids are RNA and DNA. It then discusses the structures and functions of nucleotides, nucleosides and nucleotides. Some key points include that nucleotides serve as energy carriers in cells and are components of coenzymes. The document also covers nitrogenous bases, purines and pyrimidines found in nucleic acids. It discusses how nucleotides join to form polynucleotides like DNA and RNA. In summary, the document provides an in-depth overview of the structures and roles of nucleotides, nucleic acids, DNA and RNA in the cell.
UNIT IV Nucleic acid metabolism and genetic information.pptxAshwiniBhoir2
Biosynthesis of purine and pyrimidine nucleotides
Catabolism of purine nucleotides, Hyperuricemia and Gout disease
Organization of mammalian genome
Structure of DNA and RNA and their functions
DNA replication (semi-conservative model)
Transcription or RNA synthesis
1. DNA and RNA are nucleic acids found in living organisms, with DNA serving as the genetic material in most organisms and RNA serving various roles.
2. DNA is a polymer made of nucleotides, each containing a sugar, phosphate, and nitrogenous base. The bases in DNA are adenine, guanine, cytosine, and thymine.
3. Watson and Crick discovered that DNA exists as a double helix, with the two strands linked via hydrogen bonds between complementary nucleotide base pairs.
Nucleic acids are made up of nucleotides that contain nitrogenous bases, a 5-carbon sugar (ribose in RNA and deoxyribose in DNA), and phosphate groups. Nucleotides polymerize to form either RNA or DNA, which contain the genetic material in cells. The two strands of the DNA double helix are held together through hydrogen bonding between complementary nucleotide base pairs (A-T and G-C). This discovery explained how genetic information is stored and replicated in the stable double helical structure of DNA.
This document discusses nucleotides and their metabolism. It begins by defining nucleotides and their roles in biochemical processes as the monomeric units of DNA and RNA. It then describes how purine and pyrimidine nucleotides differ based on their nitrogenous base and pentose residue, and how DNA contains deoxyribonucleotides while RNA contains ribonucleotides. The document goes on to explain that inosine monophosphate is the initially synthesized purine derivative, and that AMP and GMP are subsequently synthesized from this intermediate via separate pathways. It concludes by outlining the first step in pyrimidine ring synthesis and the synthesis of thymine from dUMP.
Aamir Khan presented to Dr. Muhammad Ateeq Qurashi on DNA and RNA on July 24th, 2018. The presentation discussed the history and discovery of nucleic acids including DNA and RNA. It explained the structures of DNA and RNA, including that DNA is a double-stranded helix composed of nucleotides with base pairing between adenine and thymine or cytosine and guanine. RNA also contains nucleotides but with uracil instead of thymine and a ribose sugar instead of deoxyribose in DNA.
DNA is composed of nucleotides that contain nitrogen bases, sugars, and phosphates. The order of these nucleotides determines the genetic code. DNA exists as a double helix structure with two complementary strands joined by hydrogen bonds between nitrogen bases on each strand. This double helix structure allows DNA to efficiently store and replicate genetic information.
The document discusses nucleic acids, their structure and functions. It describes that nucleic acids are important macromolecules found in living cells, and there are two main types - DNA and RNA. DNA has a double helix structure composed of nucleotides with deoxyribose sugar and bases of adenine, guanine, cytosine and thymine. DNA stores the genetic information in cells and determines the structure of proteins. Applications of understanding DNA include producing insulin, growth hormones and vaccines using recombinant DNA technology.
Nucleic acids are macromolecules made of nucleotides that contain three components: a 5-carbon sugar, phosphate group, and nitrogenous base. DNA and RNA are the two main types of nucleic acids. DNA contains the sugar deoxyribose and has a double helix structure, while RNA contains the sugar ribose and is single-stranded. Both are composed of nucleotides joined by phosphodiester bonds and function to carry genetic information for protein synthesis. Their primary differences are that DNA contains the base thymine while RNA contains uracil, and DNA is generally found in the nucleus while RNA has additional roles in the cytoplasm.
Nucleic acids are macromolecules made of nucleotides that contain three components: a 5-carbon sugar, phosphate group, and nitrogenous base. DNA and RNA are the two main types of nucleic acids. DNA contains the sugar deoxyribose and has a double helix structure, while RNA contains the sugar ribose and is single-stranded. Both are composed of nucleotides joined by phosphodiester bonds and function to carry genetic information for protein synthesis. Their primary differences are that DNA contains the base thymine while RNA contains uracil, and RNA is found in the cytoplasm while DNA remains in the nucleus.
i. Nucleic acids like DNA and RNA store genetic information that cells use to make proteins. DNA contains the blueprint of life and stores instructions for making proteins. RNA plays a role in converting the information from DNA into proteins. ii. DNA and RNA are made up of nucleotides, which consist of a nitrogenous base, a pentose sugar, and phosphoric acid. The sugar in DNA is deoxyribose while in RNA it is ribose. DNA contains the bases adenine, thymine, cytosine and guanine, while RNA contains uracil instead of thymine. iii. The nucleic acids DNA and RNA play essential roles in storing and using the genetic information that directs the functions of living organisms.
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Denis is a dynamic and results-driven Chief Information Officer (CIO) with a distinguished career spanning information systems analysis and technical project management. With a proven track record of spearheading the design and delivery of cutting-edge Information Management solutions, he has consistently elevated business operations, streamlined reporting functions, and maximized process efficiency.
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Date: May 29, 2024
Tags: Information Security, ISO/IEC 27001, ISO/IEC 42001, Artificial Intelligence, GDPR
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2. NUCLEOSIDE
A nucleoside is composed of purine and pyrimidine
base and sugar.
Nucleosides are classified based on the nitrogneous
base present as purine nucleosides or pyrimidine
nucleosides
In the case of purine nucleosides, the sugar is
attached to N-9 of purine ring where as in pyrimidine
nucleosides the sugar is attached to N-1 of pyrimidine
ring.
The type of linkage is N-glycosidic and sugar can be
ribose or deoxyribose.
3. PURINE NUCLEOSIDE
They contain purine bases adenine and guanine.
Adenosine is nucleoside of adenine and guanosine is the nucleoside of
guanine.
If adenine is linked to deoxyribose then it is named as deoxy adenosine
Adenosine = Adenine+Ribose
Guanosine = Guanine+Ribose
4. UNUSUAL NUCLEOSIDES
Ribothymidine and pseudouridine are examples of unusual
nucleosides.
Ribothymidine consist of thymine and ribose. It is present in
ribonucleic acids (RNA) which is not usually found.
Pseudouridine is an unusual nucleoside of uracil.
In this nucleoside carbon–carbon bonding occurs between
uracil and ribose instead of the carbon –nitrogen bond.
5. Pyrimidine nucleosides
These nucleosides are composed of pyrimidine bases.
Cytosine, Uracil and thymine are pyrimidine nitrogenous bases.
Cytidine is nucleoside of cytosine.
Uridine and thymidine are nucleosides of uracil and thymine
respectively.
Cytidine = Cytosine + Ribose
Uridine = Uracil + Ribose
Thymidine = Thymine+ Ribose
6. NUCLEOTIDES
They are phosphorylated nucleosides.
A nucleotide consist of nitrogenous base, sugar and phosphate.
Nucleotide = Purine or Pyrimidine base + Sugar + Phosphate
7. IMPORTANT BIOLOGICAL FUNCTIONS OF NUCLEOTIDES
AND NUCLEOSIDES.
1. Nucleotides are involved in signal transduction.
2. Nucleotides are required for the formation of nucleic acids.
3. Nucleotides are high energy compounds.
4. Nucleotides are components of some water soluble vitamin
coenzymes.
5. Nucleotides serve as second messengers. Many hormones
mediate their action through second messengers.
6. Some nucleotides function as donors of sugars, nitrogenous
compounds and phosphates.
7. Nucleosides function as carriers or donors of groups.
8. Nucleoside analogs are used as anti cancer agents.
9. Some nucleotides function as alarmones. They alarm cell when
something goes wrong in the cell.
8. Synthetic analogs of purines, pyrimidines and nucleosides
Some synthetic purine and pyrimidine analogs are used as anticancer
agents and antiviral gents.
Purine analogs are mercaptopurine, thioguanine, aminopurine etc.
Pyrimidine analog is 5- fluro uracil.
Nucleoside analogs are used as anticancer agents, antiviral agents
and mutagens.
Deazauridine, 6-aza uridine, ara-A, ara-C and fluro deoxyuridine are
nucleoside analogs used as anticancer agents.
Azidothymidine(AZT), dideoxy cytidine and iododeoxyuridine are
used as anti viral agents.
Bromodeoxy uridine is used as mutagen.
9. Pharmacologically important purines
Caffeine of coffee, theophylline of tea and theobromine of tea are
some purines of pharmacological importance.
Caffeine and theophylline act as CNS stimulants.
Inhalers used by asthma patients contains theophylline. It releives
nasal and bronchial congestion of these patients.
10. Nucleotides of biochemical ( Physiological) importance
Cells present in various organs of human body and other mammals
contain several free nucleotides.
These free nucleotides are involved in many biochemical or biological
processess
11. Adenine nucleotides and their physiological importance
1. Adenosine triphosphate (ATP), adenosine diphosphate (ADP) and
adenosine
monophosphate (AMP) are most important adenine nucleotides.
2. ATP, ADP, and AMP are high energy compounds.
3. ATP is popularly called as 'energy currency' of cell. Energy
exchange in biochemical reactions occurs through ATP.
4. ADP is required for the formation of ATP in electron transport
chain and in energy yielding reactions.
5. cAMP, a cyclic nucleotide of adenine is known as second
messenger. Many hormones action occurs through cAMP.
6. Many coenzymes of water soluble vitamins contain adenine
nucleotides. For example NAD, FAD, NADP, coenzyme A and
cobamide coenzymes.
12. 7. PAPS (Phospho adenosine phosphosulfate) serve as donor of
sulfate in biosynthetic reactions.
8. ATP is required for replication and protein biosynthesis.
9. Some adenosine nucleotides are involved in blood pressure
and platelet function.
10 Diadenosine nucleotides are neurotransmitters.
11. Oligoadenylate mediates action of interferon.
12. Poly adenylate serve as tail of mRNA
13. Guanine nucleotides and their physiological importance
1. Like ATP, ADP; Guanosine triphosphate (GTP) and guanosine
diphosphate (GDP) also exist in cells.
2. GTP and GDP are high energy compounds.
3. Cyclic GMP or cGMP mediates actions of several hormones.
4. GTP and GDP are components of G-proteins which are involved
in signal transduction
of several physiological processes like taste, odor, vision, metabolic
regulation etc.
5. GTP is required for replication and protein biosynthesis.
6. Guanine nucleotides are required for catalytic function of
ribonucleic acids or ribozymes.
7. Mucopolysacharide formation requires guanine nucleotides.
14. Cytosine nucleotides of physiological importance
1. CTP (Cytidine triphosphate), CDP (Cytidine diphosphate) and
CMP(Cytidine monophsphate), are high energy compounds.
2. Cyclic CMP or cCMP also occurs in cells.
3. CDP, CMP serve as donor of nitrogenous compounds during
biosynthesis.
4. CMP-NANA serve as donor of NANA in the biosynthesis of
gangliosides.
5. CDP- choline serve as donor of choline in phospholipids
biosynthesis.
15. Uracil nucleotides of physiological importance
1. UTP(Uridine triphosphate), UDP (Uridine diphosphate) and
UMP (Uridine monophosphate) are high energy compounds.
2. UDP- Glucuronic acid serve as donor of glucuronic acid in the
synthesis of mucopolysacharides, bilirubin diglucuronide and
detoxification reactions.
3. UDP is carner of sugar and aminosugars needed for synthesis
of glycogen, gangliosides, glycoproteins etc.
16. Thymine nucleotides of physiological importance
1. TTP(thymidine triphosphate), TDP(thymidine diphosphate) and
TMP( thymidine monophosphate) are high energy compounds.
2. TTP and d TTP are used for the synthesis of nucleic acids.
17. Hypoxanthine and xanthine
These are purine bases not found in nucleic acids. But their nucleotides have
important role in metabolism.
1. IDP (inosine diphosphate), IMP (inosine monophosphate) are nucleotides of
hypoxanthine. They are high energy compounds.
2. IMP is intermediate in purine nucleotide biosynthesis.
3. XMP (xanthosine monophosphate) is an intermediate in purine nucleotide
biosynthesis.
18. NUCLEIC ACIDS
Two types of nucleic acids are found in cells. They are deoxy
ribonucleic acid (DNA) and ribonucleic acid (RNA).
Pentose sugar in DNA is deoxyribose where as in RNA it is ribose.
Due to deoxyribose nucleotides present in DNA are known as
deoxy ribonucleotides. They are designated as dADP, dATP; dGDP,
dGTP, dTTP, dTDP, dCTP, dCDP etc.
Both DNA and RNA are polymers of nucleotides and often
referred as polynucleotides.
19. DNA structure
1. It consist of two polynucleotide chains.
2. These polynucleotide chains coil along long axis in the form
double helix.
3. Each polynucleotide is made up of four types of nucleotides.
4. Individual nucleotides are joined by phosphodiester bonds.
5. Four types of nucleotides are present in two chains. They are
adenylicacid, guanylic acid, cytidylic acid and thymidylic acid.
6. Each polynucleotide chain or strand has direction or polarity
and 5‘ and 3'ends.
7. These ends may be in either free form or phosphorylated
form.
20. 8. The two strands are complementary to each other.
9. Base composition of a strand is complementary to opposite
strand. If thymine is found in one strand adenine appears in
opposite strand and vice versa. Like wise if guanine appears in one
strand cytosine is found in opposite strand and vice versa.
10. Further bases of opposite strands are involved in pairing. It is
popularly known as base pairing rule. Adenine of one strand pairs
with thymine of opposite strand through two hydrogen bonds.
Guanine of a strand pairs with cytosine of opposite strand through
three hydrogen bonds.
22. 11. Due to the presence of three hydrogen bonds GC pair is
stronger than AT pair.
12. This base pairing makes copying mechanism simple and
easier.
13. Complementary nature of two strands and base pairing rule
are most outstanding features of Watson-Crick model.
14. The base pairs are stacked. The pitch of the helix is 34 A and
contain ten base pairs. The width of the helix is 20 A .
15. Due to the presence of hydrogen bonds throughout the
molecule DNA is highly stable.
16. Major and minor grooves are present on the double helix.
17. Watson- Crick model DNA is known as B-DNA.
23. Functions DNA
1. DNA is genetic material of living organisms. It contains all the information
needed for the development of entire organism or individual.
2. DNA is transferred from parent to the offspring or generation to
generation.
3. DNA contains information required for formation of individuals proteins.
4. Information is present in DNA in the form of genes.
5. Amount of DNA present in the cell of an organism depends on complexity
of organisms.
6. Human cells contain more DNA than bacterial cells or viruses.
7. DNA amount in given cell is independent of nutritional or metabolic state
of the organism.
8. DNA flows from generation to generation in any given species.
9. DNA determines physical fitness of an organism or susceptibility to disease.
24. RNA
There are three types of RNAs in cells. They are present in prokaryotes
as well as eukaryotes.
They are
(1). Messenger RNA or mRNA
(2). Transfer RNA or tRNA
(3). Ribosomal RNA or rRNA.
25. MESSENGER RNA
1. Majority of mRNA molecules are linear polymers.
2. They contain about 1000-10, 000 nucleotides.
3. They have 3' or 5' free or phosphorylated ends
4. Life span of m RNA molecules varies from few minutes to days.
5. Some RNAs have secondary structure.
6. Intra strand base pairing among complementary bases leads to
folding of linear molecules
into hair pin like secondary structure.
7. In some m RNA at 5'and 3' ends special nucleotides or sequences
occurs.
8. Poly A tail is present in some mRNAs at 3' end.
9. At 5' end some mRNA are capped. Methylated GTP is cap.
10. At 5' and an AG rich shine – Dalgarno sequence is present in
some mRNAs
26. Functions
1. mRNA carries genetic information from nucleus to cytoplasm.
2. Generally one mRNA contains information for formation one
protein.
3. The sequence of mRNA is complementary to strand from which it is
copied.
4. In mRNA genetic information is present in the form of genetic
code.
5. Occasionally one mRNA contains information for the formation of
more than one protein.
27. Transfer RNA (tRNA)
It is smallest of all RNAs and contains up to 100 nucleotides.
It contains several unusual bases like pseudouridine, dihydro
uracil, mythylated adenine and guanine and isopentenyl adenine etc.
Due to intra strand base pairing between complementary bases
tRNA molecules exist in characteristic secondary structure shape.
Secondary structure of tRNAs is in the form of clover leaf.
28. Structural features of tRNA
1. It contains an aminoacid arm at 3' end CCA is characteristic sequence of
aminoacid arm.
2. An arm containing unusual pseudouridine and ribothymidine. Hence it is
known as TφC arm
in which pseudouridine is indicated with psi ( φ ) symbol.
3. An anticodon arm containing IGC sequence. Generally this arm recognizes
codon on mRNA.
4. Dihydrouridine (UH ) arm or DHU arm that contains dihydrouracil.
5. A guanine containing 5'end.
29. Functions
1. It serve as adaptor molecule in protein biosynthesis. It carries amino
acids to site of protein synthesis.
2. For every aminoacid one specific tRNA molecule exist.
3. Stability of eukaryotic and prokaryotic tRNA varies.
30. Ribosomal RNA ( rRNA)
It is found in combination with proteins in ribosomes. It contains about 100-600
nucleotides.
Prokaryotic and eukaryotic ribosomes contain several RNA that differ in
sedimentation coefficient.
Due to intra strand base pairing between complementary bases secondary
structures are found in rRNA molecules.
They are known as domains. 16S rRNA with 1500 nucleotides has
four major domains.
31. Functions
1. It is involved in initiation of protein synthesis.
2. It is required for the formation of ribosomes.
32. Differences between DNA and RNA
• DNA
1. Double stranded molecule
2. Found in combination with proteins.
3. Pentose sugar is deoxyribose.
4. Sum of the purine bases is equal to
sum of pyrimidine bases. A+G=C+T
5. Pyrimidine base uracil is absent.
6. Only one form of DNA
predominantly occurs.
7. Resistant to alkaline hydrolysis.
8. Modified bases are usually absent.
9. Lacks catalytic activity.
• RNA
1. Single stranded molecule.
2. Except rRNA other RNAs exist as free
molecules
3. Pentose sugar is ribose.
4. Sum of purine bases is not equal to sum
of pyrimidine bases.
5. Thymine a pyrimidine base is not usually
found.
6. More than three types of RNAs occurs.
7. Easily hydrolyzed by alkali.
8. Unusual and modified bases are found.
9. Some RNAs act as enzymes or posses
catalytic
activity