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 The Golgi apparatus, also known as the Golgi complex, Golgi body, or
simply the Golgi, is an organelle found in most eukaryotic cells.
 Part of the endomembrane system in the cytoplasm, it packages
proteins into membrane-bound vesicles inside the cell before the vesicles
are sent to their destination.
 It resides at the intersection of the secretory, lysosomal,
and endocytic pathways.
 It is of particular importance in processing proteins for secretion,
containing a set of glycosylation enzymes that attach various sugar
monomers to proteins as the proteins move through the apparatus.
 It was identified in 1897 by the Italian scientist Camillo Golgi and was
named after him in 1898.
Subcellular localization
 The subcellular localization of the Golgi apparatus varies
among eukaryotes.
 In mammals, a single Golgi apparatus is usually located near
the cell nucleus, close to the centrosome.
 In yeast, multiple Golgi apparatuses are scattered throughout the
cytoplasm (as observed in Saccharomyces cerevisiae).
 In plants, Golgi stacks are not concentrated at the centrosomal
region and do not form Golgi ribbons.
 The common feature among Golgi is that they are adjacent
to endoplasmic reticulum (ER) exit sites.
Structure
 In most eukaryotes, the Golgi apparatus is made up of a series of
compartments and is a collection of fused, flattened membrane-enclosed
disks known as cisternae (singular: cisterna, also called "dictyosomes"),
originating from vesicular clusters that bud off the endoplasmic reticulum.
 A mammalian cell typically contains 40 to 100 stacks of cisternae.
 This collection of cisternae is broken down into cis, medial,
and trans compartments, making up two main networks: the cis Golgi
network (CGN) and the trans Golgi network (TGN).
 The CGN is the first cisternal structure, and the TGN is the final, from
which proteins are packaged into vesicles destined to lysosomes, secretory
vesicles, or the cell surface.
 In all eukaryotes, each cisternal stack has a cis entry face
and a trans exit face.
 These faces are characterized by unique morphology
and biochemistry.
 Within individual stacks are assortments
of enzymes responsible for selectively modifying protein
cargo. These modifications influence the fate of the
protein.
Distribution
 The Golgi apparatus tends to be larger and more
numerous in cells that synthesize and secrete large
amounts of substances; for example, the antibody-
secreting plasma B cells of the immune system have
prominent Golgi complexes.
Function
 The Golgi apparatus is a major collection and dispatch station of protein
products received from the endoplasmic reticulum (ER).
 Proteins synthesized in the ER are packaged into vesicles, which then fuse with
the Golgi apparatus. These cargo proteins are modified and destined for
secretion via exocytosis or for use in the cell.
 The Golgi apparatus is also involved in lipid transport and lysosome formation.
 The structure and function of the Golgi apparatus are intimately linked.
Individual stacks have different assortments of enzymes, allowing for
progressive processing of cargo proteins as they travel from the cisternae to the
trans Golgi face.
 Enzymatic reactions within the Golgi stacks occur exclusively
near its membrane surfaces, where enzymes are anchored.
 This feature is in contrast to the ER, which has soluble proteins
and enzymes in its lumen.
 Much of the enzymatic processing is post-translational
modification of proteins. For example, phosphorylation
of oligosaccharides on lysosomal proteins occurs in the early
CGN. Cis cisterna are associated with the removal
of mannose residues.
Vesicular transport
 The vesicles that leave the rough endoplasmic reticulum are transported to
the cis face of the Golgi apparatus, where they fuse with the Golgi
membrane and empty their contents into the lumen.
 Once inside the lumen, the molecules are modified, then sorted for
transport to their next destinations.
 Those proteins destined for areas of the cell other than either
the endoplasmic reticulum or the Golgi apparatus are moved through the
Golgi cisternae towards the trans face, to a complex network of membranes
and associated vesicles known as the trans-Golgi network (TGN).
 This area of the Golgi is the point at which proteins are sorted and shipped
to their intended destinations
3 types of vesicles formed are:
Exocytotic
vesicles (constitutive)
Vesicle contains proteins
destined
for extracellular release.
Antibody release by
activated plasma B cells
Secretory
vesicles (regulated)
Vesicles contain proteins
destined for extracellular
release. After packaging, the
vesicles bud off and are
stored in the cell until a
signal is given for their
release. When the
appropriate signal is
received they move toward
the membrane and fuse to
release their contents.
Neurotransmitter release
from neurons
Lysosomal vesicles Vesicles contain proteins
and ribosomes destined for
the lysosome, a
degradative organelle .
Digestive proteases destine
d for the lysosome

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Golgi apparatus

  • 1. VIDEO LESSON available @biOlOgy BINGE-insight learning (youtube channel)
  • 2.  The Golgi apparatus, also known as the Golgi complex, Golgi body, or simply the Golgi, is an organelle found in most eukaryotic cells.  Part of the endomembrane system in the cytoplasm, it packages proteins into membrane-bound vesicles inside the cell before the vesicles are sent to their destination.  It resides at the intersection of the secretory, lysosomal, and endocytic pathways.  It is of particular importance in processing proteins for secretion, containing a set of glycosylation enzymes that attach various sugar monomers to proteins as the proteins move through the apparatus.  It was identified in 1897 by the Italian scientist Camillo Golgi and was named after him in 1898.
  • 3. Subcellular localization  The subcellular localization of the Golgi apparatus varies among eukaryotes.  In mammals, a single Golgi apparatus is usually located near the cell nucleus, close to the centrosome.  In yeast, multiple Golgi apparatuses are scattered throughout the cytoplasm (as observed in Saccharomyces cerevisiae).  In plants, Golgi stacks are not concentrated at the centrosomal region and do not form Golgi ribbons.  The common feature among Golgi is that they are adjacent to endoplasmic reticulum (ER) exit sites.
  • 4. Structure  In most eukaryotes, the Golgi apparatus is made up of a series of compartments and is a collection of fused, flattened membrane-enclosed disks known as cisternae (singular: cisterna, also called "dictyosomes"), originating from vesicular clusters that bud off the endoplasmic reticulum.  A mammalian cell typically contains 40 to 100 stacks of cisternae.  This collection of cisternae is broken down into cis, medial, and trans compartments, making up two main networks: the cis Golgi network (CGN) and the trans Golgi network (TGN).  The CGN is the first cisternal structure, and the TGN is the final, from which proteins are packaged into vesicles destined to lysosomes, secretory vesicles, or the cell surface.
  • 5.
  • 6.  In all eukaryotes, each cisternal stack has a cis entry face and a trans exit face.  These faces are characterized by unique morphology and biochemistry.  Within individual stacks are assortments of enzymes responsible for selectively modifying protein cargo. These modifications influence the fate of the protein.
  • 7. Distribution  The Golgi apparatus tends to be larger and more numerous in cells that synthesize and secrete large amounts of substances; for example, the antibody- secreting plasma B cells of the immune system have prominent Golgi complexes.
  • 8. Function  The Golgi apparatus is a major collection and dispatch station of protein products received from the endoplasmic reticulum (ER).  Proteins synthesized in the ER are packaged into vesicles, which then fuse with the Golgi apparatus. These cargo proteins are modified and destined for secretion via exocytosis or for use in the cell.  The Golgi apparatus is also involved in lipid transport and lysosome formation.  The structure and function of the Golgi apparatus are intimately linked. Individual stacks have different assortments of enzymes, allowing for progressive processing of cargo proteins as they travel from the cisternae to the trans Golgi face.
  • 9.  Enzymatic reactions within the Golgi stacks occur exclusively near its membrane surfaces, where enzymes are anchored.  This feature is in contrast to the ER, which has soluble proteins and enzymes in its lumen.  Much of the enzymatic processing is post-translational modification of proteins. For example, phosphorylation of oligosaccharides on lysosomal proteins occurs in the early CGN. Cis cisterna are associated with the removal of mannose residues.
  • 10.
  • 11. Vesicular transport  The vesicles that leave the rough endoplasmic reticulum are transported to the cis face of the Golgi apparatus, where they fuse with the Golgi membrane and empty their contents into the lumen.  Once inside the lumen, the molecules are modified, then sorted for transport to their next destinations.  Those proteins destined for areas of the cell other than either the endoplasmic reticulum or the Golgi apparatus are moved through the Golgi cisternae towards the trans face, to a complex network of membranes and associated vesicles known as the trans-Golgi network (TGN).  This area of the Golgi is the point at which proteins are sorted and shipped to their intended destinations
  • 12.
  • 13. 3 types of vesicles formed are: Exocytotic vesicles (constitutive) Vesicle contains proteins destined for extracellular release. Antibody release by activated plasma B cells Secretory vesicles (regulated) Vesicles contain proteins destined for extracellular release. After packaging, the vesicles bud off and are stored in the cell until a signal is given for their release. When the appropriate signal is received they move toward the membrane and fuse to release their contents. Neurotransmitter release from neurons Lysosomal vesicles Vesicles contain proteins and ribosomes destined for the lysosome, a degradative organelle . Digestive proteases destine d for the lysosome