<span>Cocaine Preparations
-Coca leaves --> Coca Paste (60% pure): Not water soluble, so you can't inject it into the bloodstream -- you need an additional chemical step to turn the paste into crystal powder that can be injected or snorted
-Coca --> Cocaine Hydrochloride (99% pure): Doesn't hold up very well to heat, so you can't smoke cocaine hydrochloride
-Cocaine Hydrochloride (99% pure) --> Free-Base Cocaine or Crack Cocaine:
-Reconvert cocaine hydrochloride back to base state by removing hydrochloride from cocaine (that's why it's called free-base cocaine)
-Crack cocaine is a crystallized form, mixture of cocaine and baking soda
-75% pure
-Can be used at lower doses and is much cheaper than cocaine
-Can be smoked</span>
Answer:
This is a picture of an aminoacid chain
Explanation:
In an amino acid chain all amino acids ( for example GLY, VAL, or ARG) are linked by peptide bonds. Long chains, also called polymers, of amino acids are called proteins. The enlarged photo is an example of a structure of an amino acid. They have an amine (-NH2) and carboxyl (-COOH) functional group, along with a side chain (R group), specific to each amino acid.
Answer: D. Jacob and Monod
Explanation:
An operon is a region of DNA that consists of a single gene regulated by more than one promoter. An operon is a region of RNA that consists of the coding regions of more than one gene. RNA polymerase is the enzyme that binds to promoters and transcribes the coding regions of genes into RNA.
Jacques Monod was the first to demonstrate the preference for certain substrates over others through his studies of E. coli’s growth when cultured in the presence of two different substrates simultaneously.
Answer:
Restriction enzymes (endonucleases) are used to cut the DNA into fragements.
Explanation
Restriction enzymes are obatained from bacteria where they are utilized by bacteria for protection against viruses. Restriction enzymes are used in biotechnology research. There are several restriction enzymes and each cut the DNA at specific site known as recognition site which is usually 4-8 neucleotide long. They produce sticky ends (cutting the both DNA strand on different site) and blunt ends (cutting the both DNA strand on same site) on DNA fragments.
A mutation which occurs when a base is introduced into the DNA sequence before transcription begins will lead to frame-shift of a single base on the DNA sequence resulting in nonfunctional protein from the transcribed mRNA.
Explanation:
This change either through addition or deletion of a single base in the codon sequences of the DNA will modify the amino acid codes and will result in nonfunctional proteins after transcription.
This mutation will just result in change of a single base, i.e., it would be added either to the enhancer region or the silencer region of the sequence before the promoter which initiates transcription.
The mRNA produced due to mutated DNA sequence after the deletion or insertion point will be read as out of frame thus resulting in nonsense protein.