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PROTEIN
SYNTHESIS
PRESENTED BY
FIZA SANA-ULLAH KHAN
CONTENTS
•Transcription
•Genetic code
•tRNA
•Ribosomes
•Translation
•Polyribosomes
Transcription
DEFINITION
Transcription ,or RNA
synthesis is the process of
creating an equivalent RNA
copy of sequence of DNA.
 Both RNA and DNA are nucleic
acids , which use base pairs of
nucleotides as a complementary
language that can be converted
back and forth from DNA to RNA
in the presence of the correct
enzymes.
CENTRAL DOGMA
During transcription , a DNA sequence is
read by RNA polymerase which produces a
complementary , antiparallel RNA strand.
 As opposed to DNA replication
, transcription results in an RNA
compliment that includes
uracil(U) in all instances where
thymine(T) would have occurred
in a DNA compliment.
Transcrpition is the first step leading to gene
expression.
 The stretch of DNA transcribed into an RNA molecule
is called a transcription unit and encodes at least
one gene.
 If the gene transcribed encodes for a protein , the
result of transcription is messenger RNA (mRNA)
, which will then be used to create that protein via the
process of translation
Alternatively , the transcribed gene
may encode for either ribosomalRNA
(rRNA) or transfer RNA (tRNA) , other
components of the protein–assembly
process or other ribozymes.
 A DNA transcription unit encoding for a
protein contains not only the sequence that
will eventually be directly translated into the
protein (the coding sequence) but also
regulatory sequences that direct and regulate
the synthesis of that protein.
 As in DNA replication , DNA is read from 3'→5’
during transcription. Meanwhile , the
complementary RNA is created from the 5'→3‘
direction.
 •Only one of the two DNA strands, called the
template strand,is used for transcription.
 •The other DNA strand is called the coding
strand, because its sequence is the same as
the newly created RNA transcript (except for
the substitution of uracil for thymine).
•Transcription is divided into 3 stages:
1.initiation
2.elongation
3.termination.
Initiation
 In bacteria, transcription begins with the
binding of RNA polymerase to the promoter
in DNA.
 RNA polymerase is a core enzyme consisting
of five subunits: 2αsubunits,1β
subunit,1β'subunit,and1ωsubunit
 At the start of initiation, the core enzyme is
associated with a sigma factor that aids in
finding the appropriate – 35 and-10 base
pairs downstream of promoter sequences.
Elongation
 One strand of DNA, the template strand (or non
coding strand) ,isused as a template for RNA
synthesis.
 As transcription proceeds, RNA polymerase
traverses the template strand and uses base pairing
complementarity with the DNA template to create an
RNA copy.
 Although RNA polymerase traverses the template
strand from 3'→5', the coding (non- template)
strand and newly-formed RNA can also be used as
reference points, so transcription can be described
as occurring 5'→3'.
Elongation
 This produces an RNA molecule from 5'→3', an exact
copy of the coding strand(except that thymines are
replaced with uracils , and the nucleotides are
composed of a ribose (5- carbon) sugar where DNA
has deoxyribose (one less oxygen atom)in its sugar-
phosphate backbone).
 Unlike DNA replication, mRNA transcription can
involve multiple RNA polymerases on a
single DNA template and multiple rounds of
transcription (amplification of particular mRNA), so
many mRNA molecules can be rapidly produced
from a single copy of a gene
Elongation
 Elongation also involves a proofreading
mechanism that can replace incorrectly
incorporated bases.
Termination
 Bacteria use two different
strategies for transcription
termination:
Rho-independent and
Rho-dependent
TERMINATION
 In Rho-independent transcription termination
RNA transcription stops when the newly
synthesized RNA molecule forms a G-Crich
hairpin loop followed by a run of U's , which
makes it detach from the DNA template.
Termination
 In the "Rho-dependent“ type of termination , a
protein factor called "Rho“ destabilizes the
interaction between the template and the
mRNA, thus releasing the newly synthesized mRNA
from the elongation complex.
GENETIC CODE
Properties of genetic code
 The code is universal. All prokaryotic and
eukaryotic organisms use the same codon to
specify each amino acid.
 The code is triplet. Three nucleotides make one
codon. 61 of them code for amino acids and 3
viz., UAA, UAG and UGA are nonsense codons
or chain termination codons.
 The code is degenerate. For a particular amino
acid more than one word can be used.
Properties of genetic code
 The code is non overlapping. A base in mRNA
is not used for two different codons.
 The code is commaless. There is no special
signal or commas between codons.
 The code is non ambiguous. A particular codon
will always code for the same amino
acid, wherever it is found.
Important Codon Facts
 AUG is the start codon on all viable mRNA
molecules. It also codes for the amino acid
Methionine
 UAA, UAG, UGA are stop codes.
 Many codons are degenerate --more than one
codon codes for an AA.
 43 different combinations give 64 different
codons
Amino Acid Codons
Transfer RNA
 Transfer RNA (tRNA) is a carrier
molecule which picks up amino acids
from the cytoplasm and carries them
to the mRNA / ribosome complex.
AA
Methionine
U A C
anticodon
Ribosomes
 Bacterial ribosomes consists of two subunits
of unequal size, the larger having a
sedimentation coefficient of 50 S and the
smaller of 30S.
 The two ribosomal subunits have irregular
shapes which fit together in such a way that a
cleft is formed through which mRNA passes as
the ribosome moves along it during the
translation process and from which the newly
formed polypeptide chain emerges.
Circular mRNA Visualized Circular mRNA Visualized by
Atomic Force Microscopy
by Atomic Force Microscopy
Circular mRNA Visualized by Atomic Force Microscopy
Circular mRNA visualized by Atomic
force Microscopy, pink color shows
ribosomes
Ribosomal structure
-the three tRNA binding sites are:
1. A site=holds tRNA that is carrying the next
amino acid to be added
2. P site= holds tRNA that is carrying the
growing polypeptide chain
3. E site= where discharged tRNAs leave the
ribosome
Electron Microscope View
• mRNA (purple) binds to a ribosome.
• Beads of AA’s (yellow) are joined to
form a polypeptide.
Translation
Definition:
 Process of converting information
stored in nucleic acid sequences into
proteins.
 Sequences of mRNA (messengerRNA)
are translated into unique sequence of
amino acids in polypeptide
chain(linear order is preserved
throughout !)
 Translation is the first stage of protein
biosynthesis (part of the overall process of
gene expression).
 Translation is the production of proteins by
decoding mRNA produced in transcription.
 It occurs in the cytoplasm where the
ribosomes are located.
 Ribosomes are made of a small and large
subunit which surrounds the mRNA.
 In translation, messenger RNA (mRNA) is decoded to
produce a specific polypeptide according to the rules
specified by the genetic code.
 This uses an mRNA sequence as a template to guide
the synthesis of a chain of amino acid that form a
protein.
 Many types of transcribed RNA , such as transfer
RNA, ribosomal RNA, and small nuclear RNA are not
necessarily translated into an amino acid sequence.
Translation Phases
 Translation proceeds in four phases:
 –activation,
 –initiation,
 –elongation and
 –termination
(all describing the growth of the amino acid chain, or
polypeptide that is the product of translation).
 Amino acids are brought to ribosomes and assembled
into proteins.
Activation
 In activation, the correct amino acid is
covalently bonded to the correct transfer RNA
(tRNA).
 While this is not technically a step in
translation, it is required for translation to
proceed.
 The amino acid is joined by its carboxyl group
to the 3‘ OH of the tRNA by an ester bond.
 When the tRNA has an amino acid linked to it, it
is termed "charged".
Fig. Charged mRNA(N- formyl
methionyl tRNA fmet)
Initiation
 In Prokaryotes initiation requires the large
and small ribosome subunits, the mRNA, the
initiator tRNA and three initiation factors
(IF1,IF2,IF3) and GTP. The overall sequence of
the event is as follows:
 IF3 bind to the free 30S subunit, this helps to
prevent the large subunit binding to it with out
an mRNA molecule and forming an inactive
ribosome.
 IF2 complexed with GTP and IF1 then binds to
the small subunit. It will assist the charged
initiator tRNA to bind.
Initiation
 The 30S subunit attached to an mRNA molecule
making use of the ribosome binding site (RBS) on
them RNA.
 The initiator tRNA can then bind to the complex
by base pairing of its anticodon with the AUG
codon on mRNA.
 At this point, IF3 can be released, as its role in
keeping the subunits a part and helping them
RNA to bind are complete.
 This complex is called 30S initiation complex.
Initiation
 The 50S subunit can now bind, which
displace IF1 and IF2, and the GTP is
hydrolysed in this energy consuming
step.
 This complex is called as 70S initiation
complex.
 The assembled ribosome has two tRNA
binding sites.
 These are called the A and P sites, for
aminoacyl and peptidylsites.
 The A site is where incoming aminoacyl tRNA
molecules bind, and the Psite is where the
growing polypeptide chain is usually found.
 These sites are in the cleft of small subunit
and contain adjacent codons that are being
translated.
RIBOSOMAL STRUCTURE
E
P A
Large subunit
Peptidyl-tRNA binding site
Aminoacyl-tRNA binding site
mRNA
Small subunit
3’
Exit
site
5’
One major outcome of initiation is the
placement of the initiator tRNA in the
Psite.
It is the only tRNA that does this, as all
other must enter the Asite.
Elongation
 With the formation of 70S initiation
complex the elongation cycle can
begin.
 It involves three elongation factors EF-
Tu, EF-Ts and EF-G, GTP, charged
tRNA and the 70S initiation complex.
A U G C G G U U U A G G C C C U A G
U A C
AA1
G C C
AA2
Fig. Elongation of polypeptide chain
Elongation Steps
Elongation is divided into three steps:
1. Aminoacyl tRNA delivery
 EF-Tu is required to deliver the aminoacyl
tRNA to the A site and energy is consumed in
this step by the hydrolysis of GTP.
 The released EF-Tu. GDP complex is
regenerated with the help of EF-Ts.
 In the EF-Tu EF-Ts exchange cycle EF-Ts
displaces the GDP and subsequently is
displaced itself by GTP.
Elongation Steps
The resultant EF-Tu.GTP complex
is now able to bind another
aminoacyl tRNA and deliver it to
the ribosome.
All aminoacyl tRNAs can form this
complex with EF-Tu except the
initiator tRNA.
Elongation Steps
2. Peptide bond formation
 After aminoacyl-tRNA delivery, the A- and P-
sites are both occupied and the two amino
acids that are to be joined are in close
proximity.
 The peptidyl transferase activity of the 50S
subunit can now form a peptide bond between
these two amino acids without the input of any
more energy, since energy in the form of ATP
was used to charge the tRNA.
Fig. Peptide bond formation
Peptide chain formation
A U G C G G U U U A G G C C C U A G
A U C
stopAA1 AA4AA3AA2 AA5
Elongation Steps
3.Translocation.
 A complex of EF-G (translocase) and GTP
binds to the ribosome and, in an energy
consuming step, the discharged tRNA is
ejected from the P-site, the peptidyl-tRNA is
moved from the A-site to the P-site and the
mRNA moves by one codon relative to one
codon to the ribosome.
Elongation Steps
 GDP and EF-G are released, the latter
being reusable. A new codon is now
present in the vacant A-site.
 The cycle is repeated until one of the
termination codons (UAA, UAG and UGA)
appear in the A-site.
Termination
 Termination of the polypeptide happens when
the Asite of the ribosome faces a stop codon
(UAA, UAG, or UGA).
 When this happens, no tRNA can recognize
it, but a releasing factor can recognize
nonsense codons and causes the release of
the polypeptide chain.
 The 5’end of the mRNA gives rise to the
protein's N-terminus, and the direction of
translation can therefore be stated as N->C.
methionine glycine serine isoleucine glycine alanine
stop
codon
protein
A U G G G C U C C A U C G G C G C A U A A
mRNA
start
codon
codon 2 codon 3 codon 4 codon 5 codon 6 codon 7codon 1
Termination
 Termination of polypeptide synthesis is signalled by one
of the three termination codons in them RNA (UAA, UAG
and UGA) immediately following the last amino acid
codon.
 In prokaryotes, once a termination codon occupies the
ribosomal A-site, three termination or release
factors, viz., the protein RF1, RF2 and RF3 contribute to:
 The hydrolysis of the terminal peptidyl-tRNA bond.
 Release of the free polypeptide and the last uncharged
tRNA from the P-site
 The dissociation of the 70S ribosome into its 30S and
50S subunits
Termination
 RF1 recognizes the termination codon
UAG and UAA and RF2 recognize UGA
and UAA.
 Either RF1 or RF2 binds at the
termination codon and induces
peptidyl transferase to transfer the
growing peptide chain to a water
molecule rather than to another amino
acid.
Function of RF3 is not known
Polyribosomes
 A single strand of mRNA is translated
simultaneously by many ribosomes, spaced
closely together.
 Such clusters of ribosomes are called
polysomes or polyribosomes.
 The simultaneous translation of a single
mRNA by many ribosomes allow highly
efficient use of them RNA.
THANK YOU

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Protein synthesis

  • 5. DEFINITION Transcription ,or RNA synthesis is the process of creating an equivalent RNA copy of sequence of DNA.
  • 6.  Both RNA and DNA are nucleic acids , which use base pairs of nucleotides as a complementary language that can be converted back and forth from DNA to RNA in the presence of the correct enzymes.
  • 8. During transcription , a DNA sequence is read by RNA polymerase which produces a complementary , antiparallel RNA strand.
  • 9.  As opposed to DNA replication , transcription results in an RNA compliment that includes uracil(U) in all instances where thymine(T) would have occurred in a DNA compliment.
  • 10.
  • 11. Transcrpition is the first step leading to gene expression.  The stretch of DNA transcribed into an RNA molecule is called a transcription unit and encodes at least one gene.  If the gene transcribed encodes for a protein , the result of transcription is messenger RNA (mRNA) , which will then be used to create that protein via the process of translation
  • 12. Alternatively , the transcribed gene may encode for either ribosomalRNA (rRNA) or transfer RNA (tRNA) , other components of the protein–assembly process or other ribozymes.
  • 13.  A DNA transcription unit encoding for a protein contains not only the sequence that will eventually be directly translated into the protein (the coding sequence) but also regulatory sequences that direct and regulate the synthesis of that protein.
  • 14.  As in DNA replication , DNA is read from 3'→5’ during transcription. Meanwhile , the complementary RNA is created from the 5'→3‘ direction.  •Only one of the two DNA strands, called the template strand,is used for transcription.  •The other DNA strand is called the coding strand, because its sequence is the same as the newly created RNA transcript (except for the substitution of uracil for thymine).
  • 15.
  • 16. •Transcription is divided into 3 stages: 1.initiation 2.elongation 3.termination.
  • 17. Initiation  In bacteria, transcription begins with the binding of RNA polymerase to the promoter in DNA.  RNA polymerase is a core enzyme consisting of five subunits: 2αsubunits,1β subunit,1β'subunit,and1ωsubunit  At the start of initiation, the core enzyme is associated with a sigma factor that aids in finding the appropriate – 35 and-10 base pairs downstream of promoter sequences.
  • 18. Elongation  One strand of DNA, the template strand (or non coding strand) ,isused as a template for RNA synthesis.  As transcription proceeds, RNA polymerase traverses the template strand and uses base pairing complementarity with the DNA template to create an RNA copy.  Although RNA polymerase traverses the template strand from 3'→5', the coding (non- template) strand and newly-formed RNA can also be used as reference points, so transcription can be described as occurring 5'→3'.
  • 19.
  • 20. Elongation  This produces an RNA molecule from 5'→3', an exact copy of the coding strand(except that thymines are replaced with uracils , and the nucleotides are composed of a ribose (5- carbon) sugar where DNA has deoxyribose (one less oxygen atom)in its sugar- phosphate backbone).  Unlike DNA replication, mRNA transcription can involve multiple RNA polymerases on a single DNA template and multiple rounds of transcription (amplification of particular mRNA), so many mRNA molecules can be rapidly produced from a single copy of a gene
  • 21. Elongation  Elongation also involves a proofreading mechanism that can replace incorrectly incorporated bases.
  • 22. Termination  Bacteria use two different strategies for transcription termination: Rho-independent and Rho-dependent
  • 23. TERMINATION  In Rho-independent transcription termination RNA transcription stops when the newly synthesized RNA molecule forms a G-Crich hairpin loop followed by a run of U's , which makes it detach from the DNA template.
  • 24.
  • 25. Termination  In the "Rho-dependent“ type of termination , a protein factor called "Rho“ destabilizes the interaction between the template and the mRNA, thus releasing the newly synthesized mRNA from the elongation complex.
  • 26.
  • 28. Properties of genetic code  The code is universal. All prokaryotic and eukaryotic organisms use the same codon to specify each amino acid.  The code is triplet. Three nucleotides make one codon. 61 of them code for amino acids and 3 viz., UAA, UAG and UGA are nonsense codons or chain termination codons.  The code is degenerate. For a particular amino acid more than one word can be used.
  • 29. Properties of genetic code  The code is non overlapping. A base in mRNA is not used for two different codons.  The code is commaless. There is no special signal or commas between codons.  The code is non ambiguous. A particular codon will always code for the same amino acid, wherever it is found.
  • 30.
  • 31. Important Codon Facts  AUG is the start codon on all viable mRNA molecules. It also codes for the amino acid Methionine  UAA, UAG, UGA are stop codes.  Many codons are degenerate --more than one codon codes for an AA.  43 different combinations give 64 different codons
  • 33. Transfer RNA  Transfer RNA (tRNA) is a carrier molecule which picks up amino acids from the cytoplasm and carries them to the mRNA / ribosome complex. AA Methionine U A C anticodon
  • 34. Ribosomes  Bacterial ribosomes consists of two subunits of unequal size, the larger having a sedimentation coefficient of 50 S and the smaller of 30S.  The two ribosomal subunits have irregular shapes which fit together in such a way that a cleft is formed through which mRNA passes as the ribosome moves along it during the translation process and from which the newly formed polypeptide chain emerges.
  • 35.
  • 36. Circular mRNA Visualized Circular mRNA Visualized by Atomic Force Microscopy by Atomic Force Microscopy Circular mRNA Visualized by Atomic Force Microscopy Circular mRNA visualized by Atomic force Microscopy, pink color shows ribosomes
  • 37. Ribosomal structure -the three tRNA binding sites are: 1. A site=holds tRNA that is carrying the next amino acid to be added 2. P site= holds tRNA that is carrying the growing polypeptide chain 3. E site= where discharged tRNAs leave the ribosome
  • 38.
  • 39.
  • 40.
  • 41.
  • 42. Electron Microscope View • mRNA (purple) binds to a ribosome. • Beads of AA’s (yellow) are joined to form a polypeptide.
  • 44. Definition:  Process of converting information stored in nucleic acid sequences into proteins.  Sequences of mRNA (messengerRNA) are translated into unique sequence of amino acids in polypeptide chain(linear order is preserved throughout !)
  • 45.  Translation is the first stage of protein biosynthesis (part of the overall process of gene expression).  Translation is the production of proteins by decoding mRNA produced in transcription.  It occurs in the cytoplasm where the ribosomes are located.  Ribosomes are made of a small and large subunit which surrounds the mRNA.
  • 46.  In translation, messenger RNA (mRNA) is decoded to produce a specific polypeptide according to the rules specified by the genetic code.  This uses an mRNA sequence as a template to guide the synthesis of a chain of amino acid that form a protein.  Many types of transcribed RNA , such as transfer RNA, ribosomal RNA, and small nuclear RNA are not necessarily translated into an amino acid sequence.
  • 47. Translation Phases  Translation proceeds in four phases:  –activation,  –initiation,  –elongation and  –termination (all describing the growth of the amino acid chain, or polypeptide that is the product of translation).  Amino acids are brought to ribosomes and assembled into proteins.
  • 48. Activation  In activation, the correct amino acid is covalently bonded to the correct transfer RNA (tRNA).  While this is not technically a step in translation, it is required for translation to proceed.  The amino acid is joined by its carboxyl group to the 3‘ OH of the tRNA by an ester bond.  When the tRNA has an amino acid linked to it, it is termed "charged".
  • 49. Fig. Charged mRNA(N- formyl methionyl tRNA fmet)
  • 50. Initiation  In Prokaryotes initiation requires the large and small ribosome subunits, the mRNA, the initiator tRNA and three initiation factors (IF1,IF2,IF3) and GTP. The overall sequence of the event is as follows:  IF3 bind to the free 30S subunit, this helps to prevent the large subunit binding to it with out an mRNA molecule and forming an inactive ribosome.  IF2 complexed with GTP and IF1 then binds to the small subunit. It will assist the charged initiator tRNA to bind.
  • 51. Initiation  The 30S subunit attached to an mRNA molecule making use of the ribosome binding site (RBS) on them RNA.  The initiator tRNA can then bind to the complex by base pairing of its anticodon with the AUG codon on mRNA.  At this point, IF3 can be released, as its role in keeping the subunits a part and helping them RNA to bind are complete.  This complex is called 30S initiation complex.
  • 52. Initiation  The 50S subunit can now bind, which displace IF1 and IF2, and the GTP is hydrolysed in this energy consuming step.  This complex is called as 70S initiation complex.
  • 53.
  • 54.
  • 55.  The assembled ribosome has two tRNA binding sites.  These are called the A and P sites, for aminoacyl and peptidylsites.  The A site is where incoming aminoacyl tRNA molecules bind, and the Psite is where the growing polypeptide chain is usually found.  These sites are in the cleft of small subunit and contain adjacent codons that are being translated.
  • 56. RIBOSOMAL STRUCTURE E P A Large subunit Peptidyl-tRNA binding site Aminoacyl-tRNA binding site mRNA Small subunit 3’ Exit site 5’
  • 57. One major outcome of initiation is the placement of the initiator tRNA in the Psite. It is the only tRNA that does this, as all other must enter the Asite.
  • 58. Elongation  With the formation of 70S initiation complex the elongation cycle can begin.  It involves three elongation factors EF- Tu, EF-Ts and EF-G, GTP, charged tRNA and the 70S initiation complex.
  • 59. A U G C G G U U U A G G C C C U A G U A C AA1 G C C AA2
  • 60. Fig. Elongation of polypeptide chain
  • 61. Elongation Steps Elongation is divided into three steps: 1. Aminoacyl tRNA delivery  EF-Tu is required to deliver the aminoacyl tRNA to the A site and energy is consumed in this step by the hydrolysis of GTP.  The released EF-Tu. GDP complex is regenerated with the help of EF-Ts.  In the EF-Tu EF-Ts exchange cycle EF-Ts displaces the GDP and subsequently is displaced itself by GTP.
  • 62. Elongation Steps The resultant EF-Tu.GTP complex is now able to bind another aminoacyl tRNA and deliver it to the ribosome. All aminoacyl tRNAs can form this complex with EF-Tu except the initiator tRNA.
  • 63. Elongation Steps 2. Peptide bond formation  After aminoacyl-tRNA delivery, the A- and P- sites are both occupied and the two amino acids that are to be joined are in close proximity.  The peptidyl transferase activity of the 50S subunit can now form a peptide bond between these two amino acids without the input of any more energy, since energy in the form of ATP was used to charge the tRNA.
  • 64. Fig. Peptide bond formation
  • 65. Peptide chain formation A U G C G G U U U A G G C C C U A G A U C stopAA1 AA4AA3AA2 AA5
  • 66. Elongation Steps 3.Translocation.  A complex of EF-G (translocase) and GTP binds to the ribosome and, in an energy consuming step, the discharged tRNA is ejected from the P-site, the peptidyl-tRNA is moved from the A-site to the P-site and the mRNA moves by one codon relative to one codon to the ribosome.
  • 67. Elongation Steps  GDP and EF-G are released, the latter being reusable. A new codon is now present in the vacant A-site.  The cycle is repeated until one of the termination codons (UAA, UAG and UGA) appear in the A-site.
  • 68. Termination  Termination of the polypeptide happens when the Asite of the ribosome faces a stop codon (UAA, UAG, or UGA).  When this happens, no tRNA can recognize it, but a releasing factor can recognize nonsense codons and causes the release of the polypeptide chain.  The 5’end of the mRNA gives rise to the protein's N-terminus, and the direction of translation can therefore be stated as N->C.
  • 69. methionine glycine serine isoleucine glycine alanine stop codon protein A U G G G C U C C A U C G G C G C A U A A mRNA start codon codon 2 codon 3 codon 4 codon 5 codon 6 codon 7codon 1
  • 70. Termination  Termination of polypeptide synthesis is signalled by one of the three termination codons in them RNA (UAA, UAG and UGA) immediately following the last amino acid codon.  In prokaryotes, once a termination codon occupies the ribosomal A-site, three termination or release factors, viz., the protein RF1, RF2 and RF3 contribute to:  The hydrolysis of the terminal peptidyl-tRNA bond.  Release of the free polypeptide and the last uncharged tRNA from the P-site  The dissociation of the 70S ribosome into its 30S and 50S subunits
  • 71. Termination  RF1 recognizes the termination codon UAG and UAA and RF2 recognize UGA and UAA.  Either RF1 or RF2 binds at the termination codon and induces peptidyl transferase to transfer the growing peptide chain to a water molecule rather than to another amino acid. Function of RF3 is not known
  • 72. Polyribosomes  A single strand of mRNA is translated simultaneously by many ribosomes, spaced closely together.  Such clusters of ribosomes are called polysomes or polyribosomes.  The simultaneous translation of a single mRNA by many ribosomes allow highly efficient use of them RNA.