Unit 3 Mitochondria
Unit 3 Mitochondria
Endo-Symbiotic Hypothesis:
In this theory, the first eukaryotic cell was probably an amoeba-like cell that got
nutrients by phagocytosis and contained a nucleus that formed when a piece of the
cytoplasmic membrane pinched off around the chromosomes. Some of these amoeba-
like organisms ingested prokaryotic cells that then survived within the organism and
developed a symbiotic relationship. Mitochondria formed when bacteria capable of
aerobic respiration were ingested; chloroplasts formed when photosynthetic bacteria were
ingested. They
eventually lost their cell wall and much of their DNA because they were not of benefit
within the host cell. Mitochondria and chloroplasts cannot grow outside their host cell.
Mitochondrial Respiratory Chain:
Mitochondria is the universal Power House of the cell and harbours enzymes of both
Krebs cycle and multiprotein electron transport complexes that couple ATP synthesis to
the flow of electrons through them (oxidative phosphorylation) to oxygen.
• Complex-I:
The type-I NADH dehydrogenase complex (complex I / NADH-coenzyme Q reductase
complex / NADH ubiquinone oxidoreductase.) is structurally the most complex of the
mitochondrial electron transport complexes. Current estimates indicate that it has at
least 40 subunits.
Electron transport through complex-I (below) is reversible but it primarily oxidises
NADH generated in the mitochondrial matrix. The transfer of two electrons from NADH
to CoQ results in pumping of four protons from mitochondrial matrix to the
intermembrane space (vectorial transport; in one direction).
• Complex-II:
Complex II (succinic dehydrogenase complex; succinate: ubiquinone oxidoreductase) is
a component of both ETC and Krebs cycle.
• Complex-III:
Electron transfer through complexes I and II reduces ubiquinone to ubiquinol which in
turn is reoxidised by cyt-b/c1 complex(complex III; CoQH2: cytochrome-c
oxidoreductase).
Complex III transfers electrons to cytochrome c (cyt-c), a mobile electron carrier
bound to the outer surface of the inner mitochondrial membrane. It links complex III
and IV by transferring electrons from complex III to molecular oxygen.
• Complex-IV:
The charge difference between reduced cytochrome-c (positive) and inner
mitochondrial membrane (negative) facilitates the diffusion of cyt-c along the
membrane to cyt-a /a3 complex (complex IV; cytochrome c oxidase, COX). It is
the last complex of the respiratory chain. The multimeric complex has two heme
centres (cyt-a; cyt- a3) and two metal centres (CuA and CuB). The conserved
catalytic core has three subunits (COX 1to 3) which is mitochondrial coded in almost
all eukaryotes and many additional subunits (10-14).The complex has a large
hydrophilic region protruding into the intermembrane space, providing binding site for
cytochrome-c.
Centrosome and
its organization:
• Centrosome:
1.Discovered by:
Edouard Van Beneden
2.Name given by:
Theodor Boveri
3.Position: Near the
nucleus
• Found in animal
cell.
• Absent in higher
class plans.
• Present in lower
plants like algae, funji,
bryophytes.
• Centrosome
consists of two
centrioles, situated at right angles(90°) to each other and surrounded by clear
cytoplasm called “Centrosphere”.
• Centrosome (pair of centrioles)is also known as “Diplosome”.
• Centrioles are membraneless.
• Centrosomes are cylindrical structures.
Centriole:
• Structure: They are present in
the matrix.
1. 9+0 arrangement of
microtubules.
2. 9 microtubules are present at
the periphery in a triplet
fashion.
3. Microtubules are made up of
tubulin protein.
4. Each microtubule consists of 3
sub fibrils or tubules (triplet). Or,
“Cart Wheel Structure”
Key components labeled in the diagram include:
a. C-A Connective: Links adjacent triplet microtubules.
b. Triplet fibril: The nine sets of microtubule triplets forming the centriole’s structure.
c. Central rod (Hub): The central protein structure of the centriole.
d. 9 Spokes: Protein structures radiating from the central hub.
e. Cart-wheel structure: The characteristic arrangement of the spokes and central hub.
f. Massule or pericentriolar satellite: Structures surrounding the centriole involved in
microtubule organization.
• From outside to inside the three sub-fibres of a triplet fibril are named as C, B and A
Subfibre. A is complete with 13 protofilaments while B and C subfibres are
incomplete due to sharing of some microfilaments.
• The adjacent triplet fibrils are connected by C—A proteinaceous linkers.
• The centre of the centriole possesses a rod-shaped proteinaceous mass known as a
hub.
• From the hub, develops 9 proteinaceous strands towards the peripheral triplet
fibrils. They are called spokes. Each spoke has a thickening called X before uniting
with A sub-fibre.
• Another thickening known as Y is present nearby and is attached both to X
thickening as well as C—A linkers by connectives.