What is the monomer of atf. Organic substances - carbohydrates, proteins, lipids, nucleic acids, atp
All life on the planet consists of many cells that maintain the orderliness of their organization due to the genetic information contained in the nucleus. It is stored, implemented and transmitted by complex high-molecular compounds - nucleic acids, consisting of monomer units - nucleotides. The role of nucleic acids cannot be overestimated. The stability of their structure determines the normal vital activity of the organism, and any deviations in the structure inevitably lead to a change in the cellular organization, the activity of physiological processes and the viability of cells as a whole.
The concept of a nucleotide and its properties
Each or RNA is assembled from smaller monomeric compounds - nucleotides. In other words, a nucleotide is a building material for nucleic acids, coenzymes and many other biological compounds that are essential for a cell during its life.
The main properties of these irreplaceable substances include:
Storage of information about and inherited traits;
. exercising control over growth and reproduction;
. participation in metabolism and many other physiological processes occurring in the cell.
Speaking of nucleotides, it is impossible not to dwell on this important issue as their structure and composition.
Each nucleotide is made up of:
sugar residue;
. nitrogenous base;
. phosphate group or residue phosphoric acid.
We can say that a nucleotide is a complex organic compound. Depending on the species composition of nitrogenous bases and the type of pentose in the nucleotide structure, nucleic acids are divided into:
Deoxyribonucleic acid, or DNA;
. ribonucleic acid, or RNA.
Composition of nucleic acids
In nucleic acids, sugar is represented by pentose. This is a five-carbon sugar, in DNA it is called deoxyribose, in RNA it is called ribose. Each pentose molecule has five carbon atoms, four of which, together with an oxygen atom, form a five-membered ring, and the fifth is included in the HO-CH2 group.
The position of each carbon atom in a pentose molecule is indicated by an Arabic numeral with a prime (1C´, 2C´, 3C´, 4C´, 5C´). Since all reading processes from a nucleic acid molecule have a strict direction, the numbering of carbon atoms and their arrangement in the ring serve as a kind of indicator of the correct direction.
On the hydroxyl group, a phosphoric acid residue is attached to the third and fifth carbon atoms (3С´ and 5С´). It determines the chemical affiliation of DNA and RNA to a group of acids.
A nitrogenous base is attached to the first carbon atom (1C´) in the sugar molecule.
Species composition of nitrogenous bases
DNA nucleotides according to the nitrogenous base are represented by four types:
Adenine (A);
. guanine (G);
. cytosine (C);
. thymine (T).
The first two belong to the class of purines, the last two are pyrimidines. In terms of molecular weight, purines are always heavier than pyrimidines.
RNA nucleotides by nitrogenous base are represented by:
Adenine (A);
. guanine (G);
. cytosine (C);
. uracil (U).
Uracil, like thymine, is a pyrimidine base.
AT scientific literature you can often find another designation of nitrogenous bases - in Latin letters (A, T, C, G, U).
Let us dwell in more detail on the chemical structure of purines and pyrimidines.
Pyrimidines, namely cytosine, thymine and uracil, in their composition are represented by two nitrogen atoms and four carbon atoms, forming a six-membered ring. Each atom has its own number from 1 to 6.
Purines (adenine and guanine) are composed of pyrimidine and imidazole or two heterocycles. The purine base molecule is represented by four nitrogen atoms and five carbon atoms. Each atom is numbered from 1 to 9.
As a result of the combination of a nitrogenous base and a pentose residue, a nucleoside is formed. A nucleotide is a compound of a nucleoside and a phosphate group.
Formation of phosphodiester bonds
It is important to understand the question of how nucleotides are connected into a polypeptide chain and form a nucleic acid molecule. This happens due to the so-called phosphodiester bonds.
The interaction of two nucleotides gives a dinucleotide. The formation of a new compound occurs by condensation, when a phosphodiester bond occurs between the phosphate residue of one monomer and the hydroxy group of the pentose of another.
The synthesis of a polynucleotide is the repeated repetition of this reaction (several million times). The polynucleotide chain is built through the formation of phosphodiester bonds between the third and fifth carbons of sugars (3C' and 5C').
Polynucleotide assembly is a complex process that occurs with the participation of the enzyme DNA polymerase, which ensures the growth of the chain from only one end (3´) with a free hydroxyl group.
DNA molecule structure
A DNA molecule, like a protein, can have a primary, secondary, or tertiary structure.
The sequence of nucleotides in the DNA chain determines its primary formation due to hydrogen bonds, which are based on the principle of complementarity. In other words, during the synthesis of a double, a certain pattern operates: adenine of one chain corresponds to the thymine of the other, guanine to cytosine, and vice versa. Pairs of adenine and thymine or guanine and cytosine are formed due to two in the first and three in the last case hydrogen bonds. This combination of nucleotides provides strong connection chains and equal distance between them.
Knowing the nucleotide sequence of one DNA strand, the second one can be completed according to the principle of complementarity or addition.
The tertiary structure of DNA is formed by complex three-dimensional bonds, which makes its molecule more compact and able to fit in a small cell volume. For example, the length of DNA coli is more than 1 mm, while the length of the cell is less than 5 microns.
The number of nucleotides in DNA, namely their quantitative ratio, obeys the Chergaff rule (the number of purine bases is always equal to the number of pyrimidine bases). The distance between nucleotides is a constant value equal to 0.34 nm, as is their molecular weight.
Structure of the RNA molecule
RNA is represented by a single polynucleotide chain formed through between the pentose (in this case, ribose) and the phosphate residue. It is much shorter than DNA in length. There are also differences in the species composition of nitrogenous bases in the nucleotide. In RNA, instead of the pyrimidine base of thymine, uracil is used. Depending on the functions performed in the body, RNA can be of three types.
Ribosomal (rRNA) - usually contains from 3000 to 5000 nucleotides. As a necessary structural component, it takes part in the formation of the active center of ribosomes, the site of one of the most important processes in the cell - protein biosynthesis.
. Transport (tRNA) - consists of an average of 75 - 95 nucleotides, carries out the transfer of the desired amino acid to the site of polypeptide synthesis in the ribosome. Each type of tRNA (at least 40) has its own unique sequence of monomers or nucleotides.
. Informational (mRNA) - the nucleotide composition is very diverse. Transfers genetic information from DNA to ribosomes, acts as a matrix for the synthesis of a protein molecule.
The role of nucleotides in the body
Nucleotides in the cell perform a number of important functions:
They are used as structural blocks for nucleic acids (nucleotides of the purine and pyrimidine series);
. participate in many metabolic processes in the cell;
. are part of ATP - the main source of energy in cells;
. act as carriers of reducing equivalents in cells (NAD+, NADP+, FAD, FMN);
. perform the function of bioregulators;
. can be considered as the second messengers of extracellular regular synthesis (for example, cAMP or cGMP).
A nucleotide is a monomeric unit that forms more complex compounds - nucleic acids, without which the transfer of genetic information, its storage and reproduction is impossible. Free nucleotides are the main components involved in signaling and energy processes that support the normal functioning of cells and the body as a whole.
Home > LectureLecture 4. Nucleic acids. ATPNucleic acids. To
Rice. . DNA structure
Nucleic acids include high-polymer compounds that decompose during hydrolysis into purine and pyrimidine nitrogenous bases, pentose and phosphoric acid. Nucleic acids contain carbon, hydrogen, phosphorus, oxygen and nitrogen. There are two classes of nucleic acids: ribonucleic acids (RNA) and deoxyribonucleic acids (DNA). Structure and functions of DNA. DNA molecule - heteropolymer, whose monomers are deoxyribonucleotides. Model spatial structure DNA molecule in the form of a double helix was proposed in 1953 by J. Watson and F. Crick ( Nobel Prize), to build this model they used the work of M. Wilkins, R. Franklin, E. Chargaff. The DNA molecule is formed by two polynucleotide chains, spirally twisted around each other, and together around an imaginary axis, i.e. is a double helix (exception - some DNA-containing viruses have single-stranded DNA). The diameter of the DNA double helix is 2 nm, the distance between adjacent nucleotides is 0.34 nm, and there are 10 base pairs per turn of the helix. The length of the molecule can reach several centimeters. Molecular weight - tens and hundreds of millions. The total length of the DNA of the human cell nucleus is about 2 m. In eukaryotic cells, DNA forms complexes with proteins and has a specific spatial conformation. DNA monomer - nucleotide (deoxyribonucleotide)- consists of residues of three substances: 1) a nitrogenous base, 2) a five-carbon monosaccharide (deoxyribose) and 3) phosphoric acid. The nitrogenous bases of nucleic acids belong to the classes of pyrimidines and purines. Pyrimidine bases of DNA (have one ring in their molecule) - thymine, cytosine. Purine bases (have two rings) - adenine and guanine. O
Rice. . DNA nucleotide formation
Nucleotide formation occurs in two steps. At the first stage, as a result of the condensation reaction, nucleoside is a complex of a nitrogenous base with a sugar. In the second step, the nucleoside undergoes phosphorylation. In this case, a phosphoester bond arises between the sugar residue and phosphoric acid. Thus, a nucleotide is a nucleoside linked to a phosphoric acid residue (Fig.). The name of the nucleotide is derived from the name of the corresponding base. Nucleotides and nitrogenous bases are denoted capital letters.
nitrogenous | Name | Designation |
Adenine | Adenyl | |
Guanine | Guanyl | |
Timin | thymidyl | Fig. Dinucleotide formation |
cytosine | Cytidyl |
Rice. . DNA
Two hydrogen bonds occur between adenine and thymine, and three hydrogen bonds between guanine and cytosine. The pattern according to which the nucleotides of different DNA strands are arranged in a strictly ordered manner (adenine - thymine, guanine - cytosine) and selectively combine with each other is called the principle of complementarity.. It should be noted that J.Watson and F.Crick came to understand the principle of complementarity after reading the works of E.Chargaff. E
Rice. . Pairing of nitrogenous bases.
Chargaff, having studied great amount samples of tissues and organs of various organisms, found that in any DNA fragment the content of guanine residues always exactly corresponds to the content of cytosine, and adenine to thymine ("Chargaff's rule"), but he could not explain this fact. This provision is called "Chargaff's rule": A + GA = T; G \u003d C or --- \u003d 1 C + TI It follows from the principle of complementarity that the nucleotide sequence of one chain determines the nucleotide sequence of another. DNA chains antiparallel(opposite), that is, the nucleotides of different chains are located in opposite directions, and, therefore, opposite the 3 "end of one chain is the 5" end of the other. The DNA molecule is sometimes compared to a spiral staircase. The "railing" of this ladder is the sugar-phosphate backbone (alternating residues of deoxyribose and phosphoric acid); “steps” are complementary nitrogenous bases. The function of DNA is storage hereditary information.DNA doubling.DNA replication- the process of self-doubling, the main property of the DNA molecule. Replication belongs to the category of matrix synthesis reactions and involves enzymes. Under the action of enzymes, the DNA molecule unwinds and around each strand acting as a matrix, a new strand is completed according to the principles of complementarity and antiparallelism. Thus, in each daughter DNA, one strand is the parent strand, and the second strand is newly synthesized, this method of synthesis is called semi-conservative The "building material" and energy source for replication are deoxyribonucleoside triphosphates (ATP, TTP, GTP, CTP) containing three phosphoric acid residues. When deoxyribonucleoside triphosphates are included in the polynucleotide chain, two terminal phosphoric acid residues are cleaved off, and the released energy is used to form a phosphodiester bond between nucleotides.
Fig. DNA replication.
The following enzymes take part in replication: 1) helicases ("unwind" DNA); 2) destabilizing proteins; 3) DNA topoisomerases (cut DNA); 4) DNA polymerases (select deoxyribonucleoside triphosphates and complementarily attach them to the DNA template chain); 5) RNA primases (form RNA primers, primers); 6) DNA ligases (sew DNA fragments). With the help of helicases, DNA is untwisted in certain regions, single-stranded regions of DNA are bound by destabilizing proteins, and a replication fork is formed. With a discrepancy of 10 pairs of nucleotides (one turn of the helix), the DNA molecule must complete a complete revolution around its axis. To prevent this rotation, DNA topoisomerase cuts one strand of DNA, which allows it to rotate around the second strand. DNA polymerase can only attach a nucleotide to the 3" carbon of the deoxyribose of the previous nucleotide, so this enzyme is able to move along template DNA in only one direction: from the 3" end to the 5" end of this template DNA. Since the chains in maternal DNA are antiparallel , then on its different chains the assembly of daughter polynucleotide chains occurs in different ways and in opposite directions. leading. On the chain "5"-3"" - intermittently, in fragments ( fragments of Okazaki), which, after completion of replication by DNA ligases, are fused into one strand; this child chain will be called lagging(lagging behind). A feature of DNA polymerase is that it can only start its work with a "seed" (primer). The role of primers is performed by short RNA sequences formed with the participation of the enzyme RNA primases and paired with matrix DNA. After the completion of the assembly of polynucleotide chains, RNA primers are removed and replaced with DNA nucleotides by another DNA polymerase. Replication proceeds similarly in prokaryotes and eukaryotes. The rate of DNA synthesis in prokaryotes is an order of magnitude higher (1000 nucleotides per second) than in eukaryotes (100 nucleotides per second). Replication begins simultaneously in several regions of the DNA molecule that have a specific nucleotide sequence and are called origins(English origin - the beginning). A piece of DNA from one origin of replication to another forms a unit of replication - replicon.
Rice. . DNA replication enzymes:
1 - helicases; 2 - destabilizing proteins; 3 – leading strand of DNA; 4 - synthesis of the Okazaki fragment; 5 - the primer is replaced by DNA nucleotides and the fragments are linked by ligases; 6 - DNA polymerase; 7 - RNA primase, synthesizes RNA primer; 8 - RNA primer; 9 – Okazaki fragment; 10 - ligase, linking Okazaki fragments; 11 is a topoisomer that cuts one of the DNA strands.
R
Rice. DNA replicons
Eplication occurs before cell division. Thanks to this ability of DNA, the transfer of hereditary information from the mother cell to the daughter cells is carried out. Repair(“repair”) is the process of repairing damage to the DNA nucleotide sequence. It is carried out by special enzyme systems of the cell (repair enzymes). The following steps can be distinguished in the process of DNA structure repair: 1) DNA-repairing nucleases recognize and remove the damaged area, resulting in a gap in the DNA chain; 2) DNA polymerase fills this gap by copying information from the second (“good”) strand; 3) DNA ligase "crosslinks" the nucleotides, completing the repair.
Rice. . RNA structure
Ribonucleic acids RNA is a heteropolymer molecule whose monomers are ribonucleotides. Unlike DNA, RNA is formed not by two, but by one polynucleotide chain (exception - some RNA-containing viruses have double-stranded RNA). RNA nucleotides are able to form hydrogen bonds with each other, but these are intra-, not inter-strand bonds. RNA chains are much shorter than DNA chains. The RNA monomer - nucleotide (ribonucleotide) - consists of residues of three substances: 1) a nitrogenous base, 2) a five-carbon monosaccharide (ribose) and 3) phosphoric acid. The nitrogenous bases of RNA also belong to the classes of pyrimidines and purines. Pyrimidine bases of RNA uracil, cytosine, purine bases - adenine and guanine. AT
Rice. . tRNA
There are three types of RNA: 1) information (matrix) RNA - mRNA (mRNA), 2) transfer RNA - tRNA, 3) ribosomal RNA - rRNA. All types of RNA are unbranched polynucleotides, have a specific spatial conformation and take part in the processes of protein synthesis. Information about the structure of all types of RNA is stored in DNA. The process of synthesis of RNA on a DNA template is called transcription. Transfer RNAs- usually contain from 76 to 85 nucleotides; molecular weight - 25,000-30,000. tRNA accounts for about 10% of the total RNA content in the cell. tRNA is responsible for the transport of amino acids to the site of protein synthesis, to ribosomes. About 30 types of tRNA are found in the cell, each of them has a nucleotide sequence characteristic only for it. However, all tRNAs have several intramolecular complementary regions, due to which tRNAs acquire a clover-leaf conformation. – formation of a compact structure due to the interaction of spiralized sections of the secondary structure. Any tRNA has a loop for contact with the ribosome, an anticodon loop with an anticodon, a loop for contact with the enzyme, and an acceptor stem. The amino acid is attached to the 3 "end of the acceptor stem. Anticodon - three nucleotides that "recognize" the mRNA codon. It should be emphasized that a particular tRNA can transport a strictly defined amino acid corresponding to its anticodon. -synthetase. Ribosomal RNA- contain 3,000-5,000 nucleotides. rRNA accounts for 80-85% of the total RNA content in the cell. In combination with ribosomal proteins, rRNA forms ribosomes - organelles that carry out protein synthesis. In eukaryotic cells, rRNA synthesis occurs in the nucleolus. Information RNA varied in nucleotide content and molecular weight (up to 30,000 nucleotides). The share of mRNA accounts for up to 5% of the total RNA content in the cell. The functions of mRNA are the transfer of genetic information from DNA to ribosomes; a matrix for the synthesis of a protein molecule; determination of the amino acid sequence of the primary structure of the protein molecule. ATP, OVER + , NADP + , FAD.Adenosine triphosphoric acid (ATP) - a universal source and main energy accumulator in living cells. ATP is found in all plant and animal cells. The amount of ATP averages 0.04% (of the raw mass of the cell), the largest amount of ATP (0.2-0.5%) is found in skeletal muscles. In the cell, the ATP molecule is consumed within one minute after its formation. In humans, the amount of ATP equal to the mass body, formed and destroyed every 24 hours.ATP is a mononucleotide consisting of residues of a nitrogenous base (adenine), ribose, and three residues of phosphoric acid. Since ATP contains not one, but three phosphoric acid residues, it belongs to ribonucleoside triphosphate.For most types of work occurring in cells, the energy of ATP hydrolysis is used. At the same time, when the terminal residue of phosphoric acid is cleaved off, ATP passes into ADP (adenosine diphosphoric acid), when the second phosphoric acid residue is cleaved off, into AMP (adenosine monophosphoric acid). Exit free energy when splitting off both the terminal and the second phosphoric acid residues, it is about 30.6 kJ / mol. Cleavage of the third phosphate group is accompanied by the release of only 13.8 kJ/mol. The bonds between the terminal and the second, second and first residues of phosphoric acid are called macroergic(high-energy). ATP reserves are constantly replenished. In the cells of all organisms, ATP synthesis occurs in the process phosphorylation, i.e. addition of phosphoric acid to ADP. Phosphorylation occurs with different intensity during respiration (mitochondria), glycolysis (cytoplasm), photosynthesis (chloroplasts).
Rice. Hydrolysis of ATP
ATP is the main link between processes accompanied by the release and accumulation of energy, and processes that require energy. In addition, ATP, along with other ribonucleoside triphosphates (GTP, CTP, UTP), is a substrate for RNA synthesis. In addition to ATP, there are other molecules with macroergic bonds - UTP (uridine triphosphoric acid), GTP (guanosine triphosphoric acid), CTP (cytidine triphosphoric acid), energy which are used for the biosynthesis of protein (GTP), polysaccharides (UTP), phospholipids (CTP). But all of them are formed due to the energy of ATP. In addition to mononucleotides, important role in metabolic reactions, dinucleotides play (NAD +, NADP +, FAD), belonging to the group of coenzymes (organic molecules that remain in contact with the enzyme only during the reaction). NAD + (nicotinamide adenine dinucleotide), NADP + (nicotinamide adenine dinucleotide phosphate) are dinucleotides containing two nitrogenous bases - adenine and nicotinic acid amide - a derivative of vitamin PP), two ribose residues and two phosphoric acid residues (Fig. .). If ATP is a universal source of energy, then ABOVE + and NADP + – universal acceptors, and their restored forms - NADH and NADPH – universal donors reduction equivalents (two electrons and one proton). The nitrogen atom, which is part of the nicotinic acid amide residue, is tetravalent and carries a positive charge ( ABOVE + ). This nitrogenous base easily attaches two electrons and one proton (i.e., is reduced) in those reactions in which, with the participation of dehydrogenase enzymes, two hydrogen atoms break off from the substrate (the second proton goes into solution): Substrate-H 2 + NAD + substrate + NADH + H +
Rice. . The structure of the molecule of dinucleotides NAD + and NADP +.
A - attachment of a phosphate group to a ribose residue in the NAD molecule. B - the attachment of two electrons and one proton (H - anion) to NAD +.
In reverse reactions, enzymes, oxidizing NADH or NADPH, restore substrates by attaching hydrogen atoms to them (the second proton comes from solution). FAD - flavin adenine dinucleotide- a derivative of vitamin B 2 (riboflavin) is also a cofactor of dehydrogenases, but FAD attaches two protons and two electrons, recovering to FADH 2 .Key terms and concepts 1. DNA nucleotide. 2. Purine and pyrimidine nitrogenous bases. 3. Antiparallelism of DNA nucleotide chains. 4. Complementarity. 5. Semi-conservative mode of DNA replication. 6. Leading and lagging strands of DNA nucleotides. 7. Replicon. 8. Reparation. 9. RNA nucleotide. 10. ATP, ADP, AMP. 11. OVER +, NADP +. 12. FAD. Essential Review Questions
The joining of DNA nucleotides into one strand.
Connection of polynucleotide chains of DNA with each other.
DNA dimensions: length, diameter, length of one turn, distance between nucleotides.
Chargaff's rules, the significance of the works of D. Watson and F. Crick.
DNA replication. Enzymes that ensure replication: helicases, topoisomerases, primases, DNA polymerases; ligases.
The structure of RNA.
Types of RNA, their number, size and function.
characteristics of ATP.
Characteristics of NAD +, NADP +, FAD.
Lipids- These are organic substances that do not dissolve in water, but dissolve in organic solvents.
Lipids are divided into:
1. Fats and oils (esters of trihydric alcohol glycerol and fatty acids). Fatty acids are saturated (palmitic, stearic, arachidic) and unsaturated (oleic, linoleic, linolenic). In oils, the proportion of unsaturated fatty acids is higher, so at room temperature they are in liquid state. The fats of polar animals, compared with tropical animals, also contain more unsaturated fatty acids.
2. Lipoids (fat-like substances). These include: a) phospholipids, b) fat-soluble vitamins (A, D, E, K), c) waxes, d) simple lipids that do not contain fatty acids: steroids (cholesterol, adrenal hormones, sex hormones) and terpenes ( gibberellins - plant growth hormones, carotenoids - photosynthetic pigments, menthol).
Phospholipids have polar heads (hydrophilic regions) and non-polar tails (hydrophobic regions). Due to this structure, they play an important role in the formation of biological membranes.
Lipid functions:
1) energy - fats are a source of energy in the cell. When splitting 1 gram, 38.9 kJ of energy is released;
2) structural (building) - phospholipids are part of biological membranes;
3) protective and heat-insulating - subcutaneous fatty tissue, protects the body from hypothermia and injury;
4) storage - fats make up a supply of nutrients, being deposited in the fat cells of animals and in the seeds of plants;
5) regulatory - steroid hormones are involved in the regulation of metabolism in the body (hormones of the adrenal cortex, sex hormones).
6) source of water - when 1 kg of fat is oxidized, 1.1 kg of water is formed. It is used by desert animals, so a camel can go without drinking for 10-12 days.
Carbohydrates - complex organic substances, the general formula of which is Cn(H2O)m. They are made up of carbon, hydrogen and oxygen. In animal cells they contain 1-2%, and in plant cells up to 90% of the mass of dry matter.
Carbohydrates are divided into monosaccharides, oligosaccharides and polysaccharides.
Monosaccharides, depending on the number of carbon atoms, are divided into trioses (C3), tetroses (C4), pentoses (C5), hexoses (C6), etc. An important role in the life of the cell is played by:
1) Pentoses. Ribose and deoxyribose are constituents of nucleic acids.
2) Hexoses: glucose, fructose, galactose. Fructose is found in many fruits and honey, contributing to their sweet taste. Glucose is the main energy material in the cell during metabolism. Galactose is part of milk sugar (lactose).
D:\Program Files\Physicon\Open Biology 2.6\content\3DHTML\08010203.htm
Maltose
Oligosaccharide molecules are formed during the polymerization of 2-10 monosaccharides. When two monosaccharides are combined, disaccharides are formed: sucrose, consisting of glucose and fructose molecules; lactose, consisting of glucose and galactose molecules; Maltose is made up of two glucose molecules. In oligosaccharides and polysaccharides, monomer molecules are connected by glycosidic bonds.
Polysaccharides are formed during the polymerization of a large number of monosaccharides. Polysaccharides include glycogen (the main storage substance in animal cells); starch (the main storage substance in plant cells); cellulose (found in the cell walls of plants), chitin (found in the cell wall of fungi). The monomer of glycogen, starch and cellulose is glucose.
D:\Program Files\Physicon\Open Biology 2.6\content\3DHTML\08010208.htmCellulose
Functions of carbohydrates:
1) energy - carbohydrates are the main source of energy in the cell. When splitting 1 gram of carbohydrates, 17.6 kJ of energy is released.
2) structural (construction) - shells of plant cells are built from cellulose.
3) storage - polysaccharides serve as a reserve nutrient material.
Squirrels are biological polymers whose monomers are amino acids. Proteins are very important for cell life. They make up 50-80% of the dry matter animal cell. Proteins contain 20 different amino acids. Amino acids are divided into interchangeable, which can be synthesized in the human body, and irreplaceable (methionine, tryptophan, lysine, etc.). Essential amino acids cannot be synthesized by the human body and must be obtained from food.
Amino acid
Depending on the properties of the radical, amino acids are divided into three groups: non-polar, polar charged and polar uncharged.
Amino acids are linked together by an NH-CO bond (covalent, peptide bond). Compounds of several amino acids are called peptides. Depending on their number, di-, tri-, oligo- or polypeptides are distinguished. Typically, proteins contain 300-500 amino acid residues, but there are also larger ones containing up to several thousand amino acids. Differences in proteins are determined not only by the composition and number of amino acids, but also by the sequence of their alternation in the polypeptide chain. Levels of organization of protein molecules:
1) the primary structure is the sequence of amino acids in the polypeptide chain. Amino acids are connected by peptide bonds. The primary structure is specific to each protein and is determined by the amino acid sequence encoded in the DNA. Replacement only
one amino acid leads to a change in the functions of the protein.
2) the secondary structure is twisted into a spiral (α - spiral) or laid in the form of an accordion (β — layer) polypeptide chain. The secondary structure is supported by hydrogen bonds.
3) tertiary structure - a spiral laid in space, forming a globule or fibril. The protein is active only in the form of a tertiary structure. It is supported by disulfide, hydrogen, hydrophobic and other bonds.
4) quaternary structure - is formed by combining several proteins with primary, secondary and tertiary structures. For example, the blood protein hemoglobin consists of four globin protein molecules and a non-protein part, which is called heme.
Proteins are either simple (proteins) or complex (proteins). Simple proteins are made up of only amino acids. Complex ones contain, in addition to amino acids, other chemical compounds (for example: lipoproteins, glycoproteins, nucleoproteins, hemoglobin, etc.).
When a protein is exposed to various chemicals, high temperature protein structure is destroyed. This process is called denaturation. The process of denaturation is sometimes reversible, that is, spontaneous restoration of the protein structure can occur - renaturation. Renaturation is possible when the primary structure of the protein is preserved.
Protein Functions:
1. Structural (building) function - proteins are part of all cell membranes and cell organelles.
2. Catalytic (enzymatic) - enzyme proteins accelerate chemical reactions in the cell.
3. Motor (contractile) - proteins are involved in all types of cell movements. Thus, muscle contraction is provided by contractile proteins: actin and myosin.
4. Transport - proteins are transported chemical substances. So, the protein hemoglobin carries oxygen to organs and tissues.
5. Protective - blood proteins antibodies (immunoglobulins) recognize antigens alien to the body and contribute to their destruction.
6. Energy - proteins are the source of energy in the cell. When splitting 1 gram of proteins, 17.6 kJ of energy is released.
7. Regulatory - proteins are involved in the regulation of metabolism in the body (hormones insulin, glucagon).
8. Receptor - proteins underlie the work of receptors.
9. Storage - albumin proteins are reserve proteins of the body (egg white contains ovalbumin, milk contains lactalbumin).
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Nucleic acids biological significance
Nucleic acids
The structure of the DNA nucleotide
The structure of the RNA nucleotide
An RNA molecule is a single strand of nucleotides, similar in structure to a single strand of DNA.
Composition, properties and functions of lipids in the body
Only instead of deoxyribose, RNA includes another carbohydrate - ribose (hence the name), and instead of thymine - uracil.
complementary pairs.
In this way, principle of complementarity
G ≡ C G ≡ C
replication reparations.
Adenosine phosphoric acids - a a a
The structure of the ATP molecule:
ATP ADP + P + E
ADP AMP + F + E,
macroergic bonds
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In biology, the abbreviation ATP stands for organic matter (monomer) adenosine triphosphate(adenosine triphosphoric acid). According to the chemical structure, it is a nucleoside triphosphate. ATP is made up of ribose, adenine, three phosphoric acid residues.
Lipids. What are lipids? Classification of lipids. Lipid metabolism in the body and their biological role
The phosphates are connected in series. In this case, the last two are the so-called macroergic bond, the break of which provides the cell with a large amount of energy. Thus, ATP performs in the cell energy function.
Most of the ATP molecules are formed in mitochondria in reactions cellular respiration. In cells, there is a constant synthesis and breakdown of a large number of molecules of adenosine triphosphoric acid.
The cleavage of phosphate groups mainly occurs with the participation of the enzyme ATPases and is a hydrolysis reaction (addition of water):
ATP + H2O = ADP + H3PO4 + E,
where E is the released energy that goes to various cellular processes (the synthesis of other organic substances, their transport, the movement of organelles and cells, thermoregulation, etc.). According to various sources, the amount of released energy ranges from 30 to 60 kJ/mol.
ADP is adenosine diphosphate, which already contains two phosphoric acid residues. Most often, phosphate is then added to it again to form ATP:
ADP + H3PO4 = ATP + H2O - E.
This reaction proceeds with the absorption of energy, the accumulation of which occurs as a result of a number of enzymatic reactions and ion transfer processes (mainly in the matrix and on the inner membrane of mitochondria). Ultimately, energy is accumulated in the phosphate group attached to ADP.
However, another phosphate bound by a macroergic bond can be cleaved off from ADP, and AMP (adenosine monophosphate) is formed. AMP is part of RNA. Hence, another function of adenosine triphosphoric acid is that it serves as a source of raw materials for the synthesis of a number of organic compounds.
Thus, the structural features of ATP, its functional use only as an energy source in metabolic processes, makes it possible for cells to have a single and universal system for receiving chemical energy.
Related article: Stages of Energy Metabolism
Depending on which carbohydrate is part of the nucleotide, there are two types of nucleic acids:
1. Deoxyribonucleic acid (DNA) contains deoxyribose. A DNA macromolecule consists of 25-30 thousand or more nucleotides. The composition of the DNA nucleotide includes: deoxyribose, phosphoric acid residues (H3PO4), one of the four nitrogenous bases (adenine, guanine, cytosine, thymine).
2. Ribonucleic acid (RNA) contains ribose. An RNA macromolecule consists of 5-6 thousand nucleotides. The composition of the RNA nucleotide includes: ribose, phosphoric acid residues, one of the four nitrogenous bases (adenine, guanine, cytosine, uracil).
The monomer of DNA and RNA consists of four types of nucleotides, which differ from each other only in the nitrogenous base. Nucleotides are linked in a polymer chain. The main polymer chain is formed by a carbohydrate and phosphoric acid. Purine and pyrimidine bases are not included in the polymer chain. Moreover, the mononucleotides are linked to each other by means of diester bridges: between the OH-carbohydrate at the C3 position of one nucleotide and the OH-carbohydrate at the C5 position of the adjacent nucleotide.
Nucleic acids are characterized by primary and secondary structure. The biological function of nucleic acids in the body is determined by the primary structure, i.e., the sequence of alternation of the four types of nucleotides included in them.
Consider the secondary structure of nucleic acids using DNA as an example.
Lipids. Carbohydrates. Squirrels
DNA macromolecules are a double helix consisting of two polynucleotide chains. The residues of phosphoric acid and deoxyribose of each polynucleotide chain are located on the surface of the outer part of the helix, and nitrogenous compounds are inside. The nitrogenous bases of the two chains are linked by hydrogen bonds and they support the secondary structure. A hydrogen bond is formed between adenine and thymine, between guanine and cytosine.
The biological role of nucleic acids. They carry out the storage and transmission of hereditary information, and also determine the synthesis of the necessary proteins in the cell and its regulation. So DNA from the cell nucleus sends its RNA executors, providing them with the necessary information to the cytoplasm - the place of protein synthesis.
ATP (adenosine triphosphate) is a nucleotide consisting of a carbohydrate (ribose), three molecules of phosphoric acid and adenine. When the chemical bond between the second and third phosphate groups of ATP is hydrolyzed, energy is released. This releases energy and converts ATP to adenosine diphosphate (ADP).
If it is necessary to create a reserve of energy in the cell, then reverse process addition of a phosphate group and the conversion of ADP to ATP. Thus, ATP is able to store energy and release it. Therefore, ATP is widely used in medicine as a drug that stimulates metabolic processes in the myocardium, contributing to better oxygen uptake.
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Nucleic acids. ATP
Nucleic acids(from lat. nucleus - nucleus) - acids, first discovered in the study of the nuclei of leukocytes; were discovered in 1868 by I.F. Miescher, a Swiss biochemist. biological significance nucleic acids - storage and transmission of hereditary information; they are necessary to sustain life and to reproduce it.
Nucleic acids
The DNA nucleotide and the RNA nucleotide have similarities and differences.
The structure of the DNA nucleotide
The structure of the RNA nucleotide
The DNA molecule is a double helix strand.
An RNA molecule is a single strand of nucleotides, similar in structure to a single strand of DNA. Only instead of deoxyribose, RNA includes another carbohydrate - ribose (hence the name), and instead of thymine - uracil.
Two strands of DNA are connected to each other by hydrogen bonds. In this case, an important pattern is observed: opposite the nitrogenous base adenine A in one chain is the nitrogenous base thymine T in the other chain, and cytosine C is always located opposite the guanine G. These base pairs are called complementary pairs.
In this way, principle of complementarity(from lat. complementum - addition) is that each nitrogenous base included in the nucleotide corresponds to another nitrogenous base. There are strictly defined pairs of bases (A - T, G - C), these pairs are specific. There are three hydrogen bonds between guanine and cytosine, and between adenine and thymine, two hydrogen bonds occur in the DNA nucleotide, and in RNA, two hydrogen bonds occur between adenine and uracil.
Hydrogen bonds between nitrogenous bases of nucleotides
G ≡ C G ≡ C
As a result, in any organism, the number of adenyl nucleotides is equal to the number of thymidyl, and the number of guanyl nucleotides is equal to the number of cytidyl. Due to this property, the sequence of nucleotides in one chain determines their sequence in another. This ability to selectively combine nucleotides is called complementarity, and this property underlies the formation of new DNA molecules based on the original molecule (replication, i.e., doubling).
Thus, the quantitative content of nitrogenous bases in DNA is subject to certain rules:
1) The sum of adenine and guanine is equal to the sum of cytosine and thymine A + G = C + T.
2) The sum of adenine and cytosine is equal to the sum of guanine and thymine A + C = G + T.
3) The amount of adenine is equal to the amount of thymine, the amount of guanine is equal to the amount of cytosine A = T; G = C.
When conditions change, DNA, like proteins, can undergo denaturation, which is called melting.
DNA has unique properties: the ability to self-doubling (replication, reduplication) and the ability to self-repair (repair). replication ensures the exact reproduction in the daughter molecules of the information that was recorded in the parent molecule. But sometimes errors occur during the replication process. The ability of a DNA molecule to correct errors that occur in its chains, that is, to restore the correct sequence of nucleotides, is called reparations.
DNA molecules are found mainly in the nuclei of cells and in a small amount in mitochondria and plastids - chloroplasts. DNA molecules are carriers of hereditary information.
Structure, functions and localization in the cell. There are three types of RNA. The names are associated with the functions performed:
RNA | Location in the cell | Functions |
Ribosomal RNA (rRNA) is the largest RNA, consisting of 3 to 5 thousand nucleotides. | Ribosomes | Structural (rRNA together with a protein molecule forms a ribosome) |
Transfer RNA (tRNA) is the smallest RNA, consisting of 80-100 nucleotides. Organic substances - carbohydrates, proteins, lipids, nucleic acids, ATP |
Cytoplasm | Transfer of amino acids to ribosomes - the site of protein synthesis, codon recognition on mRNA |
Messenger, or messenger RNA (mRNA) - RNA, consisting of 300 - 3000 nucleotides. | nucleus, cytoplasm | The transfer of genetic information from DNA to the site of protein synthesis - ribosomes, is a matrix for a protein molecule (polypeptide) under construction |
Comparative characteristics of nucleic acids
Adenosine phosphoric acids - a denosine triphosphoric acid (ATP), a denosine diphosphoric acid (ADP), a denosine monophosphoric acid (AMP).
The cytoplasm of every cell, as well as mitochondria, chloroplasts and nuclei, contains adenosine triphosphate (ATP). It supplies energy for most of the reactions that take place in the cell. With the help of ATP, the cell synthesizes new molecules of proteins, carbohydrates, fats, carries out active transport of substances, beats flagella and cilia.
ATP is similar in structure to the adenine nucleotide that is part of RNA, only instead of one phosphoric acid, ATP contains three phosphoric acid residues.
The structure of the ATP molecule:
Unstable chemical bonds, which are connected to the molecules of phosphoric acid in ATP, are very rich in energy. When these bonds are broken, energy is released, which is used by each cell to ensure vital processes:
ATP ADP + P + E
ADP AMP + F + E,
where F is phosphoric acid H3PO4, E is the released energy.
Energy-rich chemical bonds in ATP between phosphoric acid residues are called macroergic bonds. The splitting of one molecule of phosphoric acid is accompanied by the release of energy - 40 kJ.
ATP is formed from ADP and inorganic phosphate due to the energy released during the oxidation of organic substances and in the process of photosynthesis. This process is called phosphorylation.
In this case, at least 40 kJ / mol of energy must be expended, which is accumulated in macroergic bonds. Consequently, the main significance of the processes of respiration and photosynthesis is determined by the fact that they supply energy for the synthesis of ATP, with the participation of which the cell performs most of work.
ATP is extremely rapidly updated. In humans, for example, each ATP molecule is broken down and rebuilt 2,400 times a day, so that its average lifespan is less than 1 minute. ATP synthesis is carried out mainly in mitochondria and chloroplasts (partially in the cytoplasm). The ATP formed here is sent to those parts of the cell where there is a need for energy.
ATP plays an important role in cell bioenergetics: it performs one of the most important functions - an energy store, it is a universal biological energy accumulator.
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Monosaccharides (simple sugars) consist of a single molecule containing 3 to 6 carbon atoms. Disaccharides are compounds formed from two monosaccharides. Polysaccharides are macromolecular substances composed of a large number(from several tens to several tens of thousands) of monosaccharides.
A variety of carbohydrates are found in large quantities in organisms. Their main functions:
- Energy: It is carbohydrates that serve as the main source of energy for the body. Among the monosaccharides, this is fructose, which is widely found in plants (primarily in fruits), and especially glucose (17.6 kJ of energy is released when one gram of it is broken down). Glucose is found in fruits and other parts of plants, in blood, lymph, animal tissues. From disaccharides, it is necessary to isolate sucrose (cane or beet sugar), consisting of glucose and fructose, and lactose (milk sugar), formed by the combination of glucose and galactose. Sucrose is found in plants (mainly in fruits), while lactose is found in milk. They play an important role in the nutrition of animals and humans. Great importance in energy processes, they have such polysaccharides as starch and glycogen, the monomer of which is glucose. They are the reserve substances of plants and animals, respectively. If there is a large amount of glucose in the body, it is used to synthesize these substances, which accumulate in the cells of tissues and organs. So, starch is found in large quantities in fruits, seeds, potato tubers; glycogen - in the liver, muscles. As needed, these substances are broken down, supplying glucose to various organs and tissues of the body.
- Structural: for example, monosaccharides such as deoxyribose and ribose are involved in the formation of nucleotides. Various carbohydrates are included cell walls(cellulose in plants, chitin in fungi).
Lipids (fats)- organic substances that are insoluble in water (hydrophobic), but readily soluble in organic solvents (chloroform, gasoline, etc.). Their molecule consists of glycerol and fatty acids. The diversity of the latter determines the diversity of lipids. Phospholipids (containing, in addition to fatty ones, a phosphoric acid residue) and glycolipids (compounds of lipids and saccharides) are widely found in cell membranes.
The functions of lipids are structural, energy and protective.
The structural basis of the cell membrane is a bimolecular (formed from two layers of molecules) layer of lipids, in which molecules of various proteins are embedded.
The breakdown of fats releases 38.9 kJ of energy, which is about twice as much as the breakdown of carbohydrates or proteins. Fats can accumulate in the cells of various tissues and organs (liver, subcutaneous tissue in animals, seeds in plants), forming a significant supply of "fuel" in the body in large quantities.
Possessing poor thermal conductivity, fats play an important role in protection against hypothermia (for example, layers of subcutaneous fat in whales and pinnipeds).
ATP (adenosine triphosphate). It serves as a universal energy carrier in cells.
Chemist's Handbook 21
The energy released during the breakdown of organic substances (fats, carbohydrates, proteins, etc.) cannot be used directly to perform any work, but is initially stored in the form of ATP.
Adenosine triphosphate consists of the nitrogenous base of adenine, ribose, and three molecules (more precisely, residues) of phosphoric acid (Fig. 1).
Rice. one. The composition of the ATP molecule
When one residue of phosphoric acid is cleaved, ADP (adenosine diphosphate) is formed and about 30 kJ of energy is released, which is spent on performing any work in the cell (for example, contraction of a muscle cell, processes of synthesis of organic substances, etc.):
Since the supply of ATP in the cell is limited, it is constantly restored due to the energy released during the breakdown of other organic substances; ATP is restored by adding a phosphoric acid molecule to ADP:
Thus, in the biological transformation of energy, two main stages can be distinguished:
1) ATP synthesis - storage of energy in the cell;
2) the release of stored energy (during the breakdown of ATP) to perform work in the cell.
Krasnodembsky E. G. "General biology: A manual for high school students and university applicants"
The most important substance in the cells of living organisms is adenosine triphosphate or adenosine triphosphate. If we enter the abbreviation of this name, we get ATP (eng. ATP). This substance belongs to the group of nucleoside triphosphates and plays a leading role in the metabolic processes in living cells, being an indispensable source of energy for them.
In contact with
The discoverers of ATP were the biochemists of the Harvard School of Tropical Medicine - Yellapragada Subbarao, Karl Loman and Cyrus Fiske. The discovery occurred in 1929 and became a major milestone in the biology of living systems. Later, in 1941, the German biochemist Fritz Lipmann found that ATP in cells is the main energy carrier.
The structure of ATP
This molecule has a systematic name, which is written as follows: 9-β-D-ribofuranosyladenine-5'-triphosphate, or 9-β-D-ribofuranosyl-6-amino-purine-5'-triphosphate. What compounds are in ATP? Chemically, it is the triphosphate ester of adenosine - derivative of adenine and ribose. This substance is formed by the connection of adenine, which is a purine nitrogenous base, with the 1'-carbon of ribose using a β-N-glycosidic bond. The α-, β-, and γ-molecules of phosphoric acid are then sequentially attached to the 5'-carbon of the ribose.
Thus, the ATP molecule contains compounds such as adenine, ribose, and three phosphoric acid residues. ATP is a special compound containing bonds that release a large amount of energy. Such bonds and substances are called macroergic. During the hydrolysis of these bonds of the ATP molecule, an amount of energy from 40 to 60 kJ / mol is released, while this process accompanied by the elimination of one or two phosphoric acid residues.
This is how these chemical reactions are written:
- one). ATP + water → ADP + phosphoric acid + energy;
- 2). ADP + water → AMP + phosphoric acid + energy.
The energy released during these reactions is used in further biochemical processes that require certain energy inputs.
The role of ATP in a living organism. Its functions
What is the function of ATP? First of all, energy. As mentioned above, the main role of adenosine triphosphate is the energy supply of biochemical processes in a living organism. This role is due to the fact that, due to the presence of two high-energy bonds, ATP acts as an energy source for many physiological and biochemical processes that require large energy costs. Such processes are all reactions of the synthesis of complex substances in the body. This is, first of all, the active transfer of molecules through cell membranes, including participation in the creation of intermembrane electrical potential, and the exercise of muscle contraction.
In addition to the above, we list a few more, no less important functions of ATP, such as:
How is ATP formed in the body?
Synthesis of adenosine triphosphoric acid is ongoing, because the body always needs energy for normal life. At any given moment, there is very little of this substance - about 250 grams, which are "emergency reserves" for a "rainy day". During illness, there is an intensive synthesis of this acid, because a lot of energy is required for the functioning of the immune and excretory systems, as well as the body's thermoregulation system, which is necessary for effective fight with an onset of illness.
Which cell has the most ATP? These are cells of muscle and nervous tissues, since energy exchange processes are most intensive in them. And this is obvious, because the muscles are involved in the movement, which requires the contraction of muscle fibers, and neurons transmit electrical impulses, without which the work of all body systems is impossible. Therefore, it is so important for the cell to maintain an unchanged and high level adenosine triphosphate.
How can adenosine triphosphate molecules be formed in the body? They are formed by the so-called phosphorylation of ADP (adenosine diphosphate). This chemical reaction as follows:
ADP + phosphoric acid + energy→ATP + water.
Phosphorylation of ADP occurs with the participation of such catalysts as enzymes and light, and is carried out in one of three ways:
Both oxidative and substrate phosphorylation use the energy of substances oxidized in the course of such synthesis.
Conclusion
Adenosine triphosphoric acid is the most frequently updated substance in the body. How long does an adenosine triphosphate molecule live on average? In the human body, for example, its life span is less than one minute, so one molecule of such a substance is born and decays up to 3000 times per day. Amazing but during the day human body synthesizes about 40 kg of this substance! So great is the need for this "internal energy" for us!
The whole cycle of synthesis and further use of ATP as an energy fuel for metabolic processes in the body of a living being is the very essence of energy metabolism in this body. Thus, adenosine triphosphate is a kind of "battery" that ensures the normal functioning of all cells of a living organism.
Carbohydrates are organic compounds containing carbon, hydrogen and oxygen. Carbohydrates are divided into mono-, di- and polysaccharides.
Monosaccharides - simple sugars, consisting of 3 or more C atoms. Monosaccharides: glucose, ribose and deoxyribose. Not hydrolysable, can crystallize, soluble in water, have a sweet taste
Polysaccharides are formed as a result of the polymerization of monosaccharides. At the same time, they lose the ability to crystallize, sweet taste. An example is starch, glycogen, cellulose.
1. Energy is the main source of energy in the cell (1 gram = 17.6 kJ)
2. structural - are part of the membranes of plant cells (cellulose) and animal cells
3. source for the synthesis of other compounds
4. storage (glycogen - in animal cells, starch - in plant cells)
5. connecting
Lipids- complex compounds of glycerol and fatty acids. Insoluble in water, only in organic solvents. Distinguish between simple and complex lipids.
Lipid functions:
1. structural - the basis for all cell membranes
2. energy (1 g = 37.6 kJ)
3. storage
4. thermal insulation
5. source of intracellular water
ATP - a single universal energy-intensive substance in the cells of plants, animals and microorganisms. With the help of ATP, energy is stored and transported in the cell. ATP is made up of the nitrogenous base adeine, the carbohydrate ribose, and three phosphoric acid residues. Phosphate groups are interconnected with the help of macroergic bonds. The functions of ATP are the transfer of energy.
Squirrels are the predominant substance in all living organisms. Protein is a polymer whose monomer is amino acids (20). Amino acids are connected in a protein molecule using peptide bonds formed between the amino group of one amino acid and the carboxyl group of another. Each cell has a unique set of proteins.
There are several levels of organization of a protein molecule. Primary structure - a sequence of amino acids connected by a peptide bond. This structure determines the specificity of the protein. In secondary the structure of the molecule has the form of a spiral, its stability is provided by hydrogen bonds. Tertiary the structure is formed as a result of the transformation of the helix into a three-dimensional spherical shape - a globule. Quaternary occurs when several protein molecules combine to form single complex. The functional activity of proteins is manifested in the 2,3, or 3rd structure.
The structure of proteins changes under the influence of various chemicals (acids, alkalis, alcohol and others) and physical factors(high and low t, radiation), enzymes. If these changes preserve the primary structure, the process is reversible and is called denaturation. The destruction of the primary structure is called coagulation(irreversible protein breakdown process)
Functions of proteins
1. structural
2. catalytic
3. contractile (proteins actin and myosin in muscle fibers)
4. transport (hemoglobin)
5. regulatory (insulin)
6. signal
7. protective
8. energy (1 g = 17.2 kJ)
Types of nucleic acids. Nucleic acids- phosphorus-containing biopolymers of living organisms that provide storage and transmission of hereditary information. They were discovered in 1869 by the Swiss biochemist F. Miescher in the nuclei of leukocytes, salmon spermatozoa. Subsequently, nucleic acids were found in all plant and animal cells, viruses, bacteria and fungi.
In nature, there are two types of nucleic acids - deoxyribonucleic (DNA) and ribonucleic (RNA). The difference in names is explained by the fact that the DNA molecule contains the five-carbon sugar deoxyribose, and the RNA molecule contains ribose.
DNA is located mainly in the chromosomes of the cell nucleus (99% of the total cell DNA), as well as in mitochondria and chloroplasts. RNA is part of ribosomes; RNA molecules are also found in the cytoplasm, matrix of plastids and mitochondria.
Nucleotides - structural components nucleic acids. Nucleic acids are biopolymers whose monomers are nucleotides.
Nucleotides- complex substances. Each nucleotide consists of a nitrogenous base, a five-carbon sugar (ribose or deoxyribose) and a phosphoric acid residue.
There are five main nitrogenous bases: adenine, guanine, uracil, thymine, and cytosine.
DNA. The DNA molecule consists of two polynucleotide chains helically twisted relative to each other.
The composition of the nucleotides of the DNA molecule includes four types of nitrogenous bases: adenine, guanine, thymine and cytocin. In a polynucleotide chain, adjacent nucleotides are linked by covalent bonds.
The DNA polynucleotide chain is twisted in the form of a spiral like a spiral staircase and is connected to another, complementary chain to it using hydrogen bonds formed between adenine and thymine (two bonds), as well as guanine and cytosine (three bonds). Nucleotides A and T, G and C are called complementary.
As a result, in any organism, the number of adenyl nucleotides is equal to the number of thymidyl, and the number of guanyl nucleotides is equal to the number of cytidyl. Due to this property, the sequence of nucleotides in one chain determines their sequence in another. This ability to selectively combine nucleotides is called complementarity, and this property underlies the formation of new DNA molecules based on the original molecule (replications, i.e. doubling).
When conditions change, DNA, like proteins, can undergo denaturation, which is called melting. With a gradual return to normal conditions, DNA renatures.
Function of DNA is the storage, transmission and reproduction in a number of generations of genetic information. The DNA of any cell encodes information about all the proteins of a given organism, about which proteins, in what sequence and in what quantity will be synthesized. The sequence of amino acids in proteins is recorded in DNA by the so-called genetic (triplet) code.
Main property DNA is its ability to replicate.
Replication - This is the process of self-duplication of DNA molecules, which occurs under the control of enzymes. Replication occurs before each nuclear division. It begins with the fact that the DNA helix is temporarily unwound under the action of the DNA polymerase enzyme. On each of the chains formed after the breaking of hydrogen bonds, a daughter strand of DNA is synthesized according to the principle of complementarity. The material for synthesis is the free nucleotides that are in the nucleus.
Thus, each polynucleotide chain plays the role matrices for a new complementary strand (therefore, the process of duplication of DNA molecules refers to the reactions matrix synthesis). The result is two DNA molecules, each of which "one chain remains from the parent molecule (half), and the other is newly synthesized. Moreover, one new chain is synthesized continuous, and the second - first in the form of short fragments, which are then sewn into a long chain a special enzyme - DNA ligase.As a result of replication, two new DNA molecules are an exact copy of the original molecule.
The biological meaning of replication lies in the exact transfer of hereditary information from the mother cell to the daughter cells, which occurs during the division of somatic cells.
RNA. The structure of RNA molecules is in many ways similar to the structure of DNA molecules. However, there are also a number of significant differences. In the RNA molecule, instead of deoxyribose, the composition of nucleotides includes ribose, and instead of the thymidyl nucleotide (T) - uridyl (U). The main difference from DNA is that the RNA molecule is a single strand. However, its nucleotides are capable of forming hydrogen bonds with each other (for example, in tRNA, rRNA molecules), but in this case we are talking about an intrastrand connection of complementary nucleotides. RNA chains are much shorter than DNA.
There are several types of RNA in the cell, which differ in the size of the molecules, structure, location in the cell and functions:
1. Information (matrix) RNA (mRNA) - transfers genetic information from DNA to ribosomes
2. Ribosomal RNA (rRNA) - is part of ribosomes
3. 3. Transfer RNA (tRNA) - transfers amino acids to ribosomes during protein synthesis
- The displacement is called the vector connecting the start and end points of the trajectory The vector connecting the beginning and end of the path is called
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