Furfural cannot be formed from ribosides until the glycosidic
linkage has been split; the purine-ribose links of RNA are easily
hydrolysed by hot acid, while the pyrimidine-ribose links are much more
resistant, and the orcinol method is commonly supposed to determine only
the purine-bound ribose of RNA.
One significance of estimation of RNA by orcinol method is the fact that it has made DNA less reactive. The test also is more sensitive with the orcinol method.
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Bial's test is used to determine the presence of a pentose sugar. For example, the sugar ribose would turn green (positive) and the sugar glucose would turn brown or yellow (negative). Nucleic acids (DNA and RNA) both contain a suger. RNA contains ribose, so it should have a positive orcinol test. DNA contains deoxyribose, which should have a weak reaction, yielding what appears to be a negative result.
RNA carries out several important roles. There are 3 main types of RNA, messenger RNA (mRNA), ribosomal RNA (rRNA) and transfer RNA (tRNA). mRNA carries a copy of the instructions for creating proteins from the DNA in the nucleus to the ribosomes for translation. rRNA makes up part of the ribosomes. tRNA carries amino acids (the building blocks of proteins) to the ribosomes
Polymerases are the enzymes that replicate and build nucleic acids. DNA polymerases synthesize DNA, RNA polymerases synthesize RNA. Purified polymerases are essential to carrying out the PCR reaction.
The "central dogma" was that the flow of information always went from DNA to RNA to protein. This assumption was discarded with the discovery of reverse transcriptase, which allowed information to move from RNA to DNA.
The initiation of the reaction is favoured energetically by formation of this RNA-DNA hybrid.This hybrid is more stronger than DNA-DNA hybrid
When orcinol reagent is added to a solution containing pentoses, a chromophore is formed that absorbs light at 660 nm. This allows for the detection and quantification of pentoses, such as ribose, in a sample. The intensity of the color generated is directly proportional to the concentration of pentoses present.
Bial's test is used to determine the presence of a pentose sugar. For example, the sugar ribose would turn green (positive) and the sugar glucose would turn brown or yellow (negative). Nucleic acids (DNA and RNA) both contain a suger. RNA contains ribose, so it should have a positive orcinol test. DNA contains deoxyribose, which should have a weak reaction, yielding what appears to be a negative result.
Orcinol reagent is used in RNA extraction to quantitate RNA by forming a colored complex with ribose sugar. The principle is based on the ability of orcinol to react with ribose sugar in RNA to produce a blue color, which can then be measured spectrophotometrically to determine RNA concentration.
Which mechanism explains the phenomenon
Yes it is the oldest and most primitive coding mechanism
natural selection favored RNA molecules that synthesized catalytic proteins
Detection of pentose/ribose sugar in RNA (by performing Bial's test) can be done with Orcinol reagent (0.3% orcinol solution prepared in concentrated HCl). This method requires the following reagents 1. Orcinol reagent : 6% orcinol in 95% ethanol. 2. Acid reagent : 100 ml. of conc. HCl, 0.5 ml. of 10% FeCl3, 10H2O is added (to an aqueous RNA solution (1 mg. per ml.)) Detection of deoxyribose/deoxypentose sugar in DNA can be identified chemically with the Dische diphenylamine test. This method requires the following reagents one gram of purified diphenylamineis dissolved in acetic acid and volume made to 100 ml. with acetic acid. Afterwards, 2.75 ml. of conc. H2SO4 is added for stablization. Schiff's reagent is another sensitive means , and can be used in a method to demonstrate deoxyribosenucleic acid (DNA) specifically (of detecting aldehydes), in contrast to unstained ribosenucleic acid (RNA). This method is the nucleal reaction of Feulgen and Rossenbeck (called the Feulgen stain or reaction). It is usually done with pararosaniline Schiff solution (pseudo-Schiff reagents), but it works well with some others, including the fluorescent acriflavine solution. This method requires the following reagents Hydrochloric acid, 1Normal Schiff's reagent (made from pararosanilin treated with sulphurous acid) Light green, 1% aqueous (can be replaced with Fast green FCF)
Antitermination of RNA synthesis is a major mechanism of regulation in prokaryotic gene expression. It allows transcription to continue past termination signals in certain conditions, enabling the production of full-length transcripts. This mechanism often involves regulatory proteins that interact with mRNA secondary structures to modulate RNA polymerase activity.
The process of forming a strand of messenger RNA from individual nucleotides is called transcription. During transcription, an enzyme called RNA polymerase helps to assemble the nucleotides in the correct sequence based on the DNA template.
For nucleic acids, commonly used testing indicators include ethidium bromide and SYBR Green, which fluoresce when bound to DNA or RNA, allowing visualization under ultraviolet light. These indicators are used in techniques like agarose gel electrophoresis and quantitative PCR to detect and quantify nucleic acids.
RNA carries out several important roles. There are 3 main types of RNA, messenger RNA (mRNA), ribosomal RNA (rRNA) and transfer RNA (tRNA). mRNA carries a copy of the instructions for creating proteins from the DNA in the nucleus to the ribosomes for translation. rRNA makes up part of the ribosomes. tRNA carries amino acids (the building blocks of proteins) to the ribosomes
Polymerases are the enzymes that replicate and build nucleic acids. DNA polymerases synthesize DNA, RNA polymerases synthesize RNA. Purified polymerases are essential to carrying out the PCR reaction.