Sunday, 24 November 2013

Diabetes Diseases and Control of Diabetes

Diabetes is Low or Not production of Insulin Hormone in the Human body. So Insulin is essential Hormone for produce energy from glucose. Therefore reduce insulin content of body; blood glucose content is rapidly increased. It is called diabetes.

When we consider diabetes in the world, there are 247 million peoples having diabetes today in the world. Normally we should test blood glucose levels in regularly. Then we can control diabetes if increase or decrease blood glucose level. When we cheek regularly blood glucose level we can understand immediately blood glucose level is high or low.
The blood glucose is change with our meals. We consider the normal range of blood glucose levels, 70 - 130 mg/dl before meals and below 180 mg/dl in 1- 2 hours after meals. A Blood glucose level is 90 - 130 mg/dl at least 8 hours after fasting.  So good method of cheek blood grouse level is cheek after 8 - 10 hours fasting, it calls Fasting Blood Sager (FBS).

Thursday, 3 October 2013

Hemophilia – Rare Bleeding Disorder

This is come to the children from there Parents through genes. So Hemophilia is a genetic disease. In the normal person, when Injury blood was clotting in short time but Hemophilia Person bleed long time and Not clotting in short time. This is rare bleeding disorder and blood does not clot normally. 



Normally chromosomes pairs come from parents and Females have 2 X chromosomes and Males have X chromosomes and Y chromosomes. Clotting factor come with X chromosomes.

Then also can bleed in side of body tissues like knees, ankles, elbows etc and this can damage some organs and tissues. To the blood clotting need clotting factor. This clotting factor is protein and Hemophilia person have little or No clotting factor. There are two types of hemophilia. They are Hemophilia A (Classic hemophilia and Factor VIII deficiency) and Hemophilia B (Christmas disease and Factor IX deficiency)

Friday, 30 August 2013

HIV - Human Immunodeficiency Virus

This HI Virus has different structure from the other retroviruses. It has composed of 2 copies of positive single stranded RNA. This single stranded RNA is tightly bound to Nucleocapsid proteins. This virus has unique life cycle and it binds to the host cells. The virus attaches with cell membrane RNA and Enzymes in the cytoplasm. HIV contain Enzyme called reverse transcriptase and this enzyme allows to single stranded RNA of virus to copied and double stranded DNA to generate.

This HI Virus is mainly to the human immune system and very dangerous virus because it course to the immunity of the human body. HIV is mainly transmission each other with body fluids likes Bloods, Semen, Pre seminal fluids, Vaginal fluids, Brest milk and Rectal mucous. But other body fluids like faces, Nasal fluid, Saliva, Sweat, tears, urine and Vomit are do not help to transmit HI virus.

There are many ways to transmitted blood fluid with each other and If some one infected with HIV they transmitted to each other. Then HIV mainly Transmitted with sexual contact like anal, Oral or virginal sex with partner. If one person infected with HIV it transmitted to other. Then child birth is other way to transmitted HIV. When child is birth of HIV can transmit with mother and child and after birth some time HIV transmitted through the Brest milk. Then it can be transmitted through the inject drugs with each other shearing needles or drugs that are contaminated with the HI virus. Some time HIV can be transmitted with the bloods transmitted to patios.

Wednesday, 17 July 2013

Down Syndrome - Genatical Deasese

Down Syndrome is a genetic. Decease and It is a congenital disorder. Most people have 23 pairs of (46 chromosomes) in there cell. But down syndrome people have extra chromosome in 21 th Par of chromosome. so there are 47 total number of chromosomes. This extra chromosomes is effect to Development of Peoples body.


When we Consider about Down syndrome children,

1. Down syndrome children are developed slower than other children
2. They have some health Problems
3. Eyes are almond shaped
4. Nose is flat
5. They have large tongue
6. Head and hands are Smaller
7. They have wide feet with Short toes
8. Tone Muscles are poor
9. More flexible joints with compare to Normal children

Some down syndrome children have more signs of above and other have few of those. Then Down syndrome appearing about one of every 800 births.

This Down syndrome chilled needs supportive and Preventive medical care to mange there life conditions. If we give good care to down syndrome chilled they can build up there life as normal child. Some child are educated and complete there degree and they build up cheerful life. So we should maintain good physical and Social condition of Down syndrome chilled.

Wednesday, 10 July 2013

Introduction about Chromosome in Cells

Chromosomes can be found in nucleus of the each living cells. That controls all the function of the cell and other control materials. The Fundamental material of chromosomes is DNA. This DNA Molecules are packaged as thread like structure and that is tightly coiled around the Proteins. This coiled like structure support to make the chromosomes structure and it is called Histones. Chromosomes are Microscopic material and can be found in cell Nucleus.
When we consider more about the Chromosomes, They have Constriction point called Centromere. Which is point that divided chromosomes to two parts called "arms". The Short arm of the chromosomes is called “P arm" and Longs arm of the chromosomes is called “Q arm"
Chromosomes are leads to Maintain characters of the cells and other all cell factions. As an example, when we consider about Human Cells Nucleus. There are 46 chromosomes and they contain as pairs so that have 23 pairs of chromosomes. All 22 Pairs of chromosomes are same in both females and Males and this 22 pairs if chromosomes are called Autosomes and lead all faction except sex characters. Other chromosomes (23 rd pair of chromosome) are different between males and Females. Female’s chromosomes fair have two copies of X chromosome and Males chromosomes fair have X chromosome and Y chromosome.

Wednesday, 3 July 2013

Introduction of Living Cells

Structural Building units of plant and Animals are called Cells. They are fundamental building blokes of life. Amount of cell are very from the type of organisms as Single cell organisms like Bacteria, malty cellular structure like Tissue, organ and Organism like plant and animals.

Cells are mostly small structure and composed with water and out of structure made by phospholipids by layer membrane. This layer is allowing to go inside and go outside to some component this is called semi permeable. Because not allow to go and come out all things. Only Permit to go some component.

Cell element contain 59% of Hydrogen (H), 24% of Oxygen (O), 11% of Carbon (C), 4 % of nitrogen and 2 % of other like prosperous (P), Sulphur (S) etc. The Cells have 90% of fluid called cytoplasm. Cytoplasm consists of Protein, Carbohydrates, fats, Free Amino acid and number of other elements. The cell Environment consists of Cytoplasm and Nucleus like DNA, RNA. This Cell environment affects Gene Expression and Gene Regulation.

Monday, 1 July 2013

DNA Viruses (Double Standard)

DNA Viruses Conceptually, the simplest viruses to understand are those with genomes of double stranded DNA (dsDNA). The nucleocapsid of this type of virus enters the cell it proceeds to the nucleus where it mimics the genome of the host cell. Usually, viral genome is replicated using the host cell DNA polymerase and viral genome is transcribed by the host cell RNA polymerase. Resulting transcripts carrying information encoding viral proteins is then transported to the cytoplasm and seen as template by the host cell Ribosomes. Some of these newly synthesized viral proteins are used as the protein capsid around newly replicated viral DNA molecules and these new virions are released from the cell, where they target other host cells and trigger new rounds of infection

Double Standard DNA viruses that exploit the host cell machinery to complete their life cycles can carry small genomes encoding mostly viral structural proteins like those for the capsid. The dependence of these viruses on the host cell replication machinery creates a potentially awkward situation; the enzymes of DNA replication are generally not expressed in quiescent cells.  Most of the cells infected will be in G and therefore inhospitable hosts. Some dsDNA viruses are herpes virus family or the Epstein Barr virus has large genomes that contain greater than sixty genes

Wednesday, 26 June 2013

The Strategies of Virus Replication

 Life cycle of most viruses is designed to maximize the production of progeny virus particles in the cells. Case of many animal viruses, the time elapsed from infection to the generation of the first progeny ranges form several hours to a day. Burden of producing a large number of virus particles causes the infected cell to die. This lysis of the host cell is called the viral lytic cycle and is an immediate and inevitable consequence of viral reproduction

In the other viruses will refrain from killing the host cell. They can establish a long term infection of the cell which cell releases a steady stream of viral particles over an extended period of time. If this continuous production of virus particles does not compromise the health of the host cell and it can live on indefinitely devoting some of its resources to making virus

Details of a viral replication cycle are dictated by the type of nucleic acid carried into the host cell by the infecting virion. Most DNA viruses enter the nucleus where they parasitize of host cell's DNA replication apparatus. There are exceptions notably the smallpox DNA virus encodes its own DNA replication machinery and thus remains in the cytoplasm. Most RNA viruses replicate in the cytoplasm because the enzymes used to replicate viral RNA are virally encoded

Wednesday, 19 June 2013

Plus ss RNA Retroviruses in Living cells

In this viruses are lipid containing viruses whose genomes can act as mRNA.  Most notorious of these is HIV and this viruses resulting in AIDS.  Aside from HIV retroviruses are rather uncommon in humans, but prevalent in other mammals and birds.  Genomes of retroviruses are similar in structure and size to picornaviruses like polio virus and one might suppose that the replicative strategy of a retrovirus resembles that of poliovirus. Life cycle of a retrovirus is unique and unusual

Plus strand of RNA is not associated with ribosomes, It has all the attributes of mRNA.  Instead and virion RNA is used as a template to make a DNA copy of the viral genome.  Copying of RNA into DNA is foreign for the host cell and must be carried out by a viral enzyme that is packaged in virion 

The viral enzyme, called reverse transcriptase carries out this process. Terms reverse and retro imply a mechanism that is the opposite of that normally operating in all cells usual flow of information in a cell is from DNA to RNA is not from RNA to DNA. Initial product of reverse transcription is an RNA and DNA hybrid double helix

RNA portion of this hybrid is degraded and reverse transcriptase copies the remaining DNA strand into dsDNA. Processes take place in the cytoplasm. The viral dsDNA is synthesized, it is transported into the nucleus where it is inserted and covalently linked to Host chromosomal DNA. Viral DNA that is integrated into the host genome is called a provirus and it is indistinguishable from the host cell genes. The retrovirus has created a version of the viral genome that has all the attributes of a cellular gene found in the host.  The integrated provirus can be transcribed by the host cell into (+) RNA that is transported to the cytoplasm and used either as mRNA in viral protein synthesis or as the genome for new progeny viruses

Tuesday, 11 June 2013

Ecology of Poliovirus (Compared to Influenza Virus)

When we Consider about Ecology of Poliovirus, the (+) ssRNA genome of poliovirus, a single long RNA molecule, is unable to recombine with (+) ssRNA genomes from other related picornaviruses by the process of crossing-over. Crossing over requires a set of highly specialized enzymes that are not available to the viruses. This means that there are only a very small number of closely related poliovirus strains and immunity against one of these strains confers immunity against the others. Influenza virus presents a dramatically contrasting example.  Influenza virus genome is composed of different RNAs, each carrying different genes

There are two different types of flu virus simultaneously infect a single host cell, two viral genomes may recombine by simply exchanging RNAs.  Progeny virion released from this cell can have RNAs from each different infecting virus and thus a new and unique strain has been created.  This is devastating consequences on human health

Natural reservoir for many flu viruses is the shore bird population around the world, which includes migratory ducks and geese.  At least a dozen distinct strains of flu virus live continually in these birds.  In rural China and other parts of the world, ducks and pigs are kept in close proximity with one another and with humans.  Ducks become infected with a flu virus originating in the wild shore birds.  They can then pass the virus to a pig, which is also readily infected by human flu viruses.  In the infected cells of the pig, the two viral genomes can mix and RNAs from both viruses can be packaged into one virion.  In this way, a new recombinant flu virus, one quite different from pre existing strains may emerge and infect humans

Exposed humans would have not experienced this strain before, and thus there is no immunity to it.  Flu virus now spreads throughout the population creating a worldwide epidemic.  These pandemics create serious respiratory infections, but usually prove lethal to only a few, mostly the weak and elderly

Wednesday, 5 June 2013

Consider about Ecology of Retroviruses

When we Consider about Ecology of Retroviruses have peculiar ecology. Retroviruses genomes can become integrated into the host cell chromosome.  Once integrated, the viral genome (pro virus) may be transcribed or it may stay dormant and unsubscribed.  If dormant, the retrovirus can exist undetected for a long time

Retroviruses have serious implications for HIV infections. HIV pro virus can integrate into the chromosome of a host white blood cell (lymphocyte) and remain undetected for years.  Only when that lymphocyte is stimulated by some physiological signal will transcription of the pro virus be activated.  Suddenly then, virus particles can burst from the cell and infect other nearby cells.  This dormant state, termed viral latency, means that it is difficult, indeed virtually impossible, to eradicate an HIV infection from the body.  Retroviruses can be many cells that harbor silent pro viruses; each is indistinguishable from a normal uninfected cells.

Saturday, 25 May 2013

The Phospolipid Bilayer

The Phospolipid BIlayer is aqueous environment inside and outside a cell prevents membrane lipids from escaping from the bilayer but nothing stops these molecules from moving about and changing places with one another within the plane of the bilayer. The membrane therefore behaves as a two dimensional fluid which is crucial for membrane function. Membranes consist largely of a lipid bilayer which is a double wall of phospoholipid, cholesterol and glycolipid molecules containing chains of fatty acids. Lipids give cell membranes a fluid character with a consistency approaching that of light oil. The fatty acid chains allow many small, fat soluble molecules such as oxygen to permeate the membrane, but they repel large water soluble molecules, such as sugar and electrically charged ions such as calcium

The top and bottom layers of the membrane have their stems facing each other. Proteins can stretch through the top bottom or both layers of phospolipid bilayer. Embedded in the lipid bilayer are large proteins many of which transport ions and water soluble molecules across the membrane. Some proteins in the plasma membrane form open pores called membrane channels which allow the free diffusion of ions into and out of the cell. Others bind to specific molecules on one side of membrane and in a process that is not clearly understood transport the molecules to the other side. Sometimes one protein simultaneously transports two types of molecules in opposite directions. Most plasma membranes are about 50 percent protein by weight while the membranes of some metabolically active organelles are 75 percent
                     
Phospolipid bilayer has 5 reasons for making it possible for the cell membrane to perform its job. Used to join cells together in cell adhesion Attach the membrane to the cytoskeleton Proteins gather together as enzymes and carry out different steps of metabolic reactions that take place near the cell membrane

Wednesday, 22 May 2013

Glycoproteins and Glycolipids in Animal and Plant Cells

The Glycolipids are located mainly in the plasma membrane and they are found only in the noncytosolic half of the bilayer. Their sugar groups therefore are exposed on the exterior of the cell where they form part of the protective coat of carbohydrate that surrounds most animal cells. This protective coat is the glycocalyx. Glycolipid molecules acquire their sugar groups in the Golgi apparatus.

Enzymes that add the sugar groups are confined to the inside of the Golgi apparatus so that the sugars are added to lipid molecules in the non cytosolic half of the lipid bilayer. Once a glycolipid molecule has been created in this way it remains trapped in this monolayer. as there are no flippases to transfer the glycolipid to the cytosolic side of the membrane.

There are Two broad types of glycolipids can be distinguished,

1. Glycerol Based
  • Fatty acid chains attached to the glycerol molecule.
  • A carbohydrate group linked to the 3rd carbon of glycerol with no bridging phosphate group
  • Glycerol based glycolipids are the primary form in plants and bacteria
2. Sphingolipid Based
  • These are based on the addition of carbohydrate units to the sphingolipid nucleus This type of glycolipid is the main form in animal cell membranes
  • Simple glycolipids formed by the addition of a single sugar unit are called cerebrosides
  • Addition of straight or branched sugar chains producesgangliosides. Carbohydrates added can be have considerablevariation in structure

Friday, 17 May 2013

Composition and Functions of Cell membranes

The Plasma membranes are made of lipids, proteins and carbohydrates

Lipids
Barrier separating the interior of the cell from its environment. Also act as a barrier between the solutions inside the cell separating contents of an organelle from the cell cytoplasm. For example: nucleus is surrounded by two layers of membranes that are actually extensions of the membrane surrounding the cell.  These nuclear membranes keep the DNA inside of the nucleus

Lipid molecules are called PHOSOPHOLIPIDS that made of fatty acids, glycerol, phosphate and hydrophilic organic derivative. Amphipathic one end of molecule is hydrophobic and the other side is hydrophillic) Fluid with the degree of un saturation of fatty acids determining the fluidity Barrier to polar molecules Basis for the cell signaling system

Proteins
The proteins within the plasma membrane are the functional part of the membrane allowing for transport of materials through the membrane AND sending and receiving signals to and from other cells

Basically these proteins can act as, pumps, gates, receptors, energy transducers and enzymes OR receptors for the endocytosis of material and cell cell signaling. The proteins associated with the outside surface of the lipid by layer are called EXTRINSIC PROTEINS. These can be easily removed

The proteins that are embedded in the membrane are called INTRINSIC PROTEINS. They can only remove with detergents that disrupt the cell membrane. Integral proteins also have a hydrophobic portion that spans the hydrophobic interior of the lipid bi layer. Some of these inner proteins also have INTEGRINS their job is to connect the outside proteins to the cytoskeleton inside the cell

Carbohydrates
Modify the lipid and protein molecules

CELL MEMBRANE (Plasma Membrne)

Cell membrane is possibly the most important organell in the cell. It holds the cell together  keeping everything intact. It is mobile and moves along paths that membranes follow. It is composed of a phosolipid bilayer

Basic Definition cell membrane
The cell membrane is the thin layer that forms the outer boundary of a living cell or of an internal cell compartment The outer boundary is the plasma membrane and compartments enclosed by internal membranes are called organelles. Cell membranes have a dual function
 (1) they both separate important but incompatible processes conducted in the organelles and keep toxic substances out of the cell
(2) they allow specific nutrients, wastes and metabolic products to pass between organelles and between the cell and the outside environment

Main Functions of cell membrane
•    Holds cell together
•    Controls whats goes out of cell
•    Controls what comes into cell
•    Manains homeostasis

The Endomembrane system

The Endomembrane system are consist of,

•    plasma membrane
•    nuclear envelope
•    endoplasmic reticulum
•    Golgi apparatus or Golgi bodies
•    vesicles
•    vaculoles
•    lysosomes

The membrane of all of these is composed of two layers of phospholipids with embedded proteins. Membrane has a consistency of a light oil allowing its membranes to diffuse throughout. Autogenous hypothesis states that the endomembrane system evolved from invagination of the plasma membrane

Monday, 13 May 2013

Double Helix DNA and Pentose Sugars

Double Helix DNA
DNA is double stranded helical model for DNA is shown in the graphic on the left. The easiest way to visualize DNA is as an immensely long rope ladder, twisted into a cork screw shape. Sides of the ladder are alternating sequences of deoxyribose and phosphate while the rungs of the ladder are made in two parts with each part firmly attached to the side of the ladder. Parts in the rung are heterocyclic amines held in position by hydrogen bonding. Then most DNA exists as open ended double helices, some bacterial DNA has been found as a cyclic helix. Some time DNA has also been found as a single strand.

Pentose Sugars in DNA
In nucleic acids two types of pentose sugars can be found. This difference is reflected in their names deoxyribonucleic acid indicates the presence of deoxyribose and ribonucleic acid indicates the presence of ribose

These sugars in the graphic on the left, the structures of both ribose and deoxyribose are shown. Note the red OH on one and the red H on the other are the only differences. The alpha and beta designations are interchangeable and are not a significant difference between these tow types

Friday, 10 May 2013

DNA Forensic and Testing

There are two main types of forensic DNA testing. RFLP and PCR based testing, although these terms are not very descriptive. Generally, RFLP testing requires larger amounts of DNA and the DNA must be underrated. Crime scene evidence that is old or that is present in small amounts is often unsuitable for RFLP testing. Warm moist conditions may accelerate DNA degradation rendering it unsuitable for RFLP in a relatively short period of time

PCR based testing often requires less DNA than RFLP testing and the DNA may be partially degraded, more so than is the case with RFLP. However, PCR still has sample size and degradation limitations that sometimes may be under appreciated. PCR based tests are also extremely sensitive to contaminating DNA at the crime scene and within the test laboratory. During PCR, contaminants may be amplified up to a billion times their original concentration. Contamination can influence PCR results, particularly in the absence of proper handling techniques and proper controls for contamination. PCR is less direct and somewhat more prone to error than RFLP. However, PCR has tended to replace RFLP in forensic testing primarily because PCR based tests are faster and more sensitive.

Structure and Replication of DNA

Bio Coach Module of DNA is designed to help you understand DNA structure and replication. As to solve problems, this will be reviewing the chemical structure of DNA and the process of DNA replication. Animations and interactive activities will enrich your review experience in a dynamic way. This module is designed to be a supplement to, but not a replacement for, your textbook and classroom notes. You can test your understanding of DNA structure and replication by using the Self Quiz at the end of the module

Thursday, 2 May 2013

Importance of Protein to Cells

Proteins are organic compounds made of amino acids arranged in a linear chain and folded into a globular form. The amino acids in a polymer are joined together by the peptide bonds between the carboxyl and amino groups of adjacent amino acid residues. The sequence of amino acids in a protein is defined by the sequence of a gene, which is encoded in the genetic code. In general, the genetic code specifies 20 standard amino acids, however, in certain organisms the genetic code can include selenocysteine and in certain archaic pyrrolysine. Shortly after or even during synthesis, the residues in a protein are often chemically modified by post-translational modification, which alters the physical and chemical properties, folding, stability, activity, and ultimately, the function of the proteins. Proteins can also work together to achieve a particular function and they often associate to form stable complexes. Of the most distinguishing features of polypeptides is their ability to fold into a global state, or "structure". The extent to which proteins fold into a defined structure varies widely. Data supports that some protein structures fold into a highly rigid structure with small fluctuations and are therefore considered to be single structure. Other proteins have been shown to undergo large rearrangements from one conformation to another. This conformational change is often associated with a signaling event. Thus, the structure of a protein serves a medium through which to regulate either the function of a protein or activity of an enzyme. Not all proteins requiring a folding process in order to function as some function in an unfolded state

Biological macromolecules such as polysaccharides and nucleic acids, proteins are essential parts of organisms and participate in virtually every process within cells. Many proteins are enzymes that catalyze biochemical reactions and are vital to metabolism. Proteins also have structural or mechanical functions, such as acting and myosin in muscle and the proteins in the cytoskeleton, which form a system of scaffolding that maintains cell shape. Other proteins are important in cell signaling, immune responses, cell adhesion, and the cell cycle. Proteins are also necessary in animals' diets, since animals cannot synthesize all the amino acids they need and must obtain essential amino acids from food

Proteins may be purified from other cellular components using a variety of techniques such as ultracentrifugation, precipitation, electrophoresis, and chromatography; the advent of genetic engineering has made possible a number of methods to facilitate purification. Methods commonly used to study protein structure and function includes immunohistochemistry, site directed mutagenesis, nuclear magnetic resonance and mass spectrometry

Biosynthesis of Protein and Method Protein Biosynthesis

The Protein synthesis is the process in which cells build proteins. Term is sometimes used to refer only to protein translation but more often it refers to a multi step process, beginning with amino acid synthesis and transcription of nuclear DNA into messenger RNA, which is then used as input to translation.

Cistron DNA is transcribed into a variety of RNA intermediates. Last version is used as a template in synthesis of a polypeptide chain. Proteins can often be synthesized directly from genes by translating mRNA. When a protein needs to be available on short notice or in large quantities, a protein precursor is produced. Proportion is an inactive protein containing one or more inhibitory peptides that can be activated when the inhibitory sequence is removed by proteolysis during posttranslational modification.

A proportion is a form that contains a signal sequence that specifies its insertion into or through membranes. Signal peptide is cleaved off in the endoplasmic reticulum. Preproproteins have both sequences still present. Synthesis of protein, a succession of tRNA molecules charged with appropriate amino acids have to be brought together with an mRNA molecule and matched up by base pairing through their anti cordons with each of its successive cordons. Amino acids then have to be linked together to extend the growing protein chain, tRNAs, relieved of their burdens, have to be released. Whole complex of processes is carried out by a giant multi molecular machine, Ribosome, formed of two main chains of RNA, called ribosomal RNA (rRNA), and more than 50 different proteins. This molecular juggernaut latches onto the end of an mRNA molecule and then trundles along it, capturing loaded tRNA molecules and stitching together the amino acids they carry to form a new protein chain. Protein biosynthesis, although very similar, is different for prokaryotes and eukaryotes

Tuesday, 30 April 2013

DNA and RNA in Animal and Plant Cells

Actually 2 main types of nucleic substances are can be found within cell nuclei that process information. DNA is the basic form within chromosomes that is hard coded into every cell. RNA is a more temporary form that is used to process subsequences of DNA messages. RNA is an intermediate form used to execute the portions of DNA that a cell is using. For example, in the synthesis of proteins, DNA is copied to RNA, which is then used to create proteins DNA->RNA->Proteins. The structure of DNA and RNA are very similar. They are both ordered sequences of 4 types of substances, ACGT for DNA and ACGU for RNA. Thus RNA uses the same three ACG substances, but uses U (uracil) instead of T (thymine). The molecules uracil and thymine are only slightly different chemically. In DNA, there is pairing between AT and CG and in RNA, the pairings are AU and CG, but since RNA is not double-stranded, this pairing is much rarer. Hence, RNA has the 4 substances,

    1    A adenosine
    2    C cytosine
    3    G guanine
    4    U uracil

DNA is created from RNA, and this is done by faithfully copying the sequence of base pairs, with the only change converting T to U. Hence, an RNA copy of a DNA sequence encodes the identical information, though it uses a slightly different set of 4 substances. The differences between DNA and RNA are also many. The underlying sugar molecule that traps the 4 bases are different is deoxyribose in DNA, ribose in RNA. DNA is two strands wrapped in a double-helix, but RNA is a single strand.

Chromosomes in Animal and Plant Cells

There are 6 billion odd base pairs are split amongst 46 chromosomes. This Each person gets 2 pairs of chromosomes, In 23 from each parent, to total 46 chromosomes per human cell. A chromosome is the largest form of a DNA molecule, with a large sequence of DNA codes, of differing lengths, usually hundreds of millions of base pairs in each chromosome. Chromosomes are independent molecules of DNA, with the typical double-helix, a start and end, but no cycles. Chromosomes are physically large enough to be seen on high power microscopes and these are very small.

Sunday, 28 April 2013

DNA Analysis and Gene Cloning

The known world wide as the standard introductory text to this important and exciting area, the fifth edition of Gene Cloning and DNA Analysis addresses new and growing areas of research whilst retaining the philosophy of the previous editions. Assuming the reader has little prior knowledge of the subject its importance, the principles of the techniques used and their applications are all carefully laid out, with over 250 clearly presented two color illustrations

In addition to a number of informative changes to the text throughout the book, the final four chapters have been significantly updated and extended to reflect the striking advances made in recent years in the applications of gene cloning and DNA analysis in biotechnology

Extended chapter on agriculture including new material on glyphosate resistant plants
New section on the uses of gene cloning and PCR in archaeology Coverage of ethical concerns relating to pharming, gene therapy and GM crops

Then Gene Cloning and DNA Analysis remains an essential introductory text to a wide range of biological sciences students, including genetics and genomics, molecular biology, biochemistry, immunology and applied biology. It is also a perfect introductory text for any professional needing to learn the basics of the subject. All libraries in universities where medical, life and biological sciences are studied and taught should have copies available on their shelves

Collagen in the Cells

The Collagen are found in tendons and other connective ligaments. Collagen have a triple helix as the major structure. Keratin structure is described more fully in the next section. The main differences in various keratins arise from their sulfur content. If there are many cysteine disulfide cross-links, then there is very little flexibility as in horns, claws, hooves, or nails. In wool, skin, and muscle proteins, there are fewer disulphide cross links which allow some stretching but returns to normal upon relaxation of tension.

Quaternary structure of collagen consists of three left handed helices twisted into a right handed coil. This structure is shown in the graphic on the left. Basic properties of collagen are rigidity and resistance to stretching. The helices are grouped in a variety of more complex fiber type structures. A rigid pattern of inter chain amide carbonyl hydrogen bonding is best accommodated by a primary amino acid sequence of,

-gly-X-pro- or -gly-X-hypro

X is any amino acid and hypro is hydroxyproline. In the graphic on the left X = arginine. Molecular model studies show that this sequence works the best for the triple helix structure. Glycine is needed because it is small and is the only amino acid which can fit in the interior of the triple helix

Friday, 26 April 2013

DNA Contraction in Bio Organism

DNA library is a collection of one organisms DNA fragments that are stored with in a host organism. DNA construct is an artificially constructed segment of nucleic acid that is going to be transplanted into target cell DNA library; the long strands of chromosomal DNA are cut into thousands of fragments. Each fragment is stored and replicated in a separate host organism, such as a bacterium. It often contains DNA insert, which contains the gene sequence encoding a protein of interest that has been sub cloned into vector, which contains bacterial resistance genes for growth of bacteria and promoters for expression in the organism. For example for the construction of human DNA library, the long strands of chromosomal DNA are cut into thousands of pieces or fragments.

Each fragment is stores and replicated in separate host organisms such as bacterium .Bacteria can quickly replicate the DNA to produce detectable quantities. DNA construct may express wild type protein, prevent the expression of certain genes by expressing competitors or inhibitors or express mutant proteins, such as deleting mutations. DNA construct is often used inn molecular biology to analysis macromolecules such as proteins. When a gene is identified and copied, it is known as cloned. Genes are sequences of DNA code for the synthesis of one or more types of RNA molecules used to make proteins.

Bio informatics in Cell Biology

Bioinformatics involved the manipulation, searching and data mining of DNA sequence data. The development of techniques to store and search DNA sequences have to lead to widely applied advances in computer science, especially string searching algorithm, machine learning and database theory.

The biological data must be combined to comprehensive picture of activities. Field of bioinformatics has evolved such that most pressing task involves the analysis.

Wednesday, 24 April 2013

What about Protein and Importance of Protein

In the animal and plants Proteins are organic compounds made of amino acids arranged in a linear chain and folded into a globular form. The amino acids in a polymer are joined together by the peptide bonds between the carboxyl and amino groups of adjacent amino acid residues. The sequence of amino acids in a protein is defined by the sequence of a gene, which is encoded in the genetic code. In general, the genetic code specifies 20 standard amino acids; however, in certain organisms the genetic code can include selenocysteine and in certain archaea pyrrolysine. Shortly after or even during synthesis, the residues in a protein are often chemically modified by post-translational modification, which alters the physical and chemical properties, folding, stability, activity, and ultimately, the function of the proteins. Proteins can also work together to achieve a particular function, and they often associate to form stable complexes of the most distinguishing features of polypeptides is their ability to fold into a globule state, or (structure). The extent to which proteins fold into a defined structure varies widely. Data supports that some protein structures fold into a highly rigid structure with small fluctuations and are therefore considered to be single structure. Other proteins have been shown to undergo large rearrangements from one conformation to another. This conformational change is often associated with a signaling event. Structure of a protein serves a medium through which to regulate either the function of a protein or activity of an enzyme. Not all proteins requiring a folding process in order to function as some function in an unfolded state

Biological macromolecules such as polysaccharides and nucleic acids, proteins are essential parts of organisms and participate in virtually every process within cells. Many proteins are enzymes that catalyze biochemical reactions and are vital to metabolism. Proteins also have structural or mechanical functions, such as actin and myosin in muscle and the proteins in the cytoskeleton, which form a system of scaffolding that maintains cell shape. Other proteins are important in cell signaling, immune responses, cell adhesion, and the cell cycle. Proteins are also necessary in animals' diets, since animals cannot synthesize all the amino acids they need and must obtain essential amino acids from food. Through the process of digestion, animals break down ingested protein into free amino acids that are then used in metabolism. Proteins were first described by the Dutch chemist Gerhardus Johannes Mulder and named by the Swedish chemist Jons Jakob Berzelius in 1838. Early nutritional scientists such as the German Carl von Voit believed that protein was the most important nutrient for maintaining the structure of the body, because it was generally believed that "flesh makes flesh. The central role of proteins as enzymes in living organisms was however not fully appreciated until 1926, when James B. Sumner showed that the enzyme urease was in fact a protein. The first protein to be sequenced was insulin, by Frederick Sanger, who won the Nobel Prize for this achievement in 1958. The first protein structures to be solved were hemoglobin and myoglobin, by Max Perutz and Sir John Cowdery Kendrew, respectively, in 1958.The three dimensional structures of both proteins were first determined by x-ray diffraction analysis; Perutz and Kendrew shared the 1962 Nobel Prize in Chemistry for these discoveries. Proteins may be purified from other cellular components using a variety of techniques such as ultracentrifugation, precipitation, electrophoresis, and chromatography; the advent of genetic engineering has made possible a number of methods to facilitate purification. Methods commonly used to study protein structure and function includes immune history chemistry, site-directed mutagenesis, nuclear magnetic resonance and mass spectrometry.

What about Protein Biosynthesis and Methods of Protein Biosynthesis

Biosynthesis of protein is the process in which cells build proteins. The term is sometimes used to refer only to protein translation but more often it refers to a multi step process, beginning with amino acid synthesis and transcription of nuclear DNA into messenger RNA, which is then used as input to translation.

Cistron DNA is transcribed into a variety of RNA intermediates. The last version is used as a template in synthesis of a polypeptide chain. Proteins can often be synthesized directly from genes by translating mRNA. When a protein needs to be available on short notice or in large quantities, a protein precursor is produced. A proprotein is an inactive protein containing one or more inhibitory peptides that can be activated when the inhibitory sequence is removed by proteolysis during posttranslational modification. A preprotein is a form that contains a signal sequence that specifies its insertion into or through membranes. Preproproteins have both sequences (inhibitory and signal) still present.For synthesis of protein, a succession of tRNA molecules charged with appropriate amino acids have to be brought together with an mRNA molecule and matched up by base-pairing through their anti codons with each of its successive codons. The amino acids then have to be linked together to extend the growing protein chain, and the tRNAs, relieved of their burdens, have to be released. This whole complex of processes is carried out by a giant multi molecular machine, the ribosome, formed of two main chains of RNA, called ribosomal RNA (rRNA), and more than 50 different proteins. This molecular juggernaut latches onto the end of an mRNA molecule and then trundles along it, capturing loaded tRNA molecules and stitching together the amino acids they carry to form a new protein chain.Protein biosynthesis, although very similar, is different for prokaryotes and eukaryotes.

DNA ( Deoxyribonucleic Acid )

DNA is the genetic material found in the cells of all living organisms. DNA is the fundamental building blocks for life. Nearly every cell  in a person's body has the same DNA. Most DNA is located in the cell nucleus (where it is called nuclear DNA), but DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA).The information in DNA is made up of four bases which combine to form chains. These bases include two purines (Adenine and Guanine) and two pyrimidines (Cytosine and Thymine). These are commonly referred to as A, G, C and T respectively. Human DNA consists of about 3 billion bases, and more than 99 percent of those bases are the same in all people. It is the order, or sequence, of these bases which determines genetic characteristics
 
Then each of the base is attached to a Sugar (S) molecule and a Phosphate (P) molecule. Together, a base, sugar, and phosphate are called a nucleotide. Nucleotides are arranged in two long strands that form a spiral called a double helix. The structure of the double helix is somewhat like a ladder, with the base pairs forming the ladder's rungs and the sugar and phosphate molecules forming the vertical sidepieces of the ladder.The number of purine bases in DNA is equal to the number of pyrimidines. This is due to the law of complimentary base pairing; which is Thymine (T) can only pair with Adenine (A) and Guanine (G) can only pair with Cytosine (C). we should Knowing this rule, we could predict the base sequence of one DNA strand if we knew the sequence of bases in the complimentary strand

Chromosome in the cells

Chromosome is the Cell material that maintain and Controls Bio characters of the cells. When a cell is getting ready to divide creating two daughter cells, it packs its DNA into bundles called chromosomes. Chromosomes are just bundles of DNA. For humans, there are consistently 23 pairs of chromosomes, each with a consistent size and shape. Chromosomes are numbered. Chromosome number 1 is the largest chromosome, chromosome number 2 a little smaller and so on. Among the 23 pairs of chromosomes there is a pair called the sex chromosomes. This is something of a misnomer, since there are many functions on the "sex" chromosomes that have nothing to do with sex. In females, the sex chromosome pair consists of two similar size chromosomes called X chromosomes. Males have one X and one small Y chromosome

Tuesday, 23 April 2013

Proteomics and Bioinformatics of living Organism

Total complement of proteins present at a time in a cell or cell type is known as its proteome and the study of such large scale data sets defines the field of proteomics, named by analogy to the related field of genomics. Key experimental techniques in proteomics include 2D electrophoresis, which allows the separation of a large number of proteins, mass spectrometry, which allows rapid high throughput identification of proteins and sequencing of peptides (most often after in-gel digestion), protein micro arrays, which allow the detection of the relative levels of a large number of proteins present in a cell, and two hybrid screening, which allows the systematic exploration of protein protein interactions.  The total complement of biologically possible such interactions is known as the interactome. A systematic attempt to determine the structures of proteins representing every possible fold is known as structural genomics

large amount of genomic and proteomic data available for a variety of organisms, including the human genome, allows researchers to efficiently identify homologous proteins in distantly related organisms by sequence alignment. Sequence profiling tools can perform more specific sequence manipulations such as restriction enzyme maps, open reading frame analyses for nucleotide sequences, and secondary structure prediction. From this data phylogenetic trees can be constructed and evolutionary hypotheses developed using special software like Clustal Wregarding the ancestry of modern organisms and the genes they express. The field of bioinformatics seeks to assemble, annotate, and analyze genomic and proteomic data, applying computational techniques to biological problems such as gene finding and cladistics

Genetic Code of DNA and RNA

Genetic code is the set of rules by which information encoded in genetic material (DNA or mRNA sequences) is translated into proteins  (amino acid sequences) by living cells. The code defines a mapping between tri nucleotide  sequences, called codons, and amino acids. With some exceptions,  a triplet codon in a nucleic acid sequence specifies a single amino acid. Because the vast majority of genes are encoded with exactly the same code (see the RNA codon table), this particular code is often referred to as the canonical or standard genetic code, or simply the genetic code, though in fact there are many variant codes. For example, protein synthesis in human mitochondria  relies on a genetic code that differs from the standard genetic code

Then Not all genetic information is stored using the genetic code. All organisms DNA contains regulatory sequences, intergenic segments, and chromosomal structural areas that can contribute greatly to phenotype. Those elements operate under sets of rules that are distinct from the codon-to-amino acid paradigm underlying the genetic code

Monday, 22 April 2013

Heterocyclic Amines in Cells

The Heterocyclic amines are sometimes called nitrogen bases or simply bases. The heterocyclic amines are derived from two root structures like  purines or pyrimidines. The purine root has both a six and a five member ring; the pyrimidine has a single six member ring.There are two major purines, adenine (A) and guanine (G), and three major pyrimidines, cytosine (C), uracil (U), and thymine (T). The structures are shown in the graphic on the left. As you can see, these structures are called "bases" because the amine groups as part of the ring or as a side chain have a basic property in water

Major difference between DNA and RNA is that DNA contains thymine, but not uracil, while RNA contains uracil but not thymine. The other three heterocyclic amines, adenine, guanine, and cytosine are found in both DNA and RNA. For convenience, you may remember, the list of heterocyclic amines in DNA by the words: The Amazing Gene Code (TAGC)

Pentose Sugars in living cells

In Living cell flasum There are two types of pentose sugars found in nucleic acids. This difference is reflected in their names deoxyribonucleic acid indicates the presence of deoxyribose,  while ribonucleic acid indicates the presence of ribose

Then In the graphic on the left, the structures of both ribose and deoxyribose are shown. Note the red  “ OH “on one and the red  “ H ” on the other are the only differences. The alpha and beta designations are interchangeable and are not a significant difference between the two