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[[File:Chloroplast diagram.svg|thumb|300px|The simplified internal structure of a chloroplast]]
[[File:Chloroplast diagram.svg|thumb|300px|The simplified internal structure of a chloroplast]]
'''[[Chloroplast]]s''' contain several important [[biological membrane|membranes]], vital for their function. Like [[mitochondria]], chloroplasts have a double-membrane envelope, called the '''chloroplast envelope'''. Each membrane is a [[phospholipid bilayer]], between 6 and 8 [[nanometre|nm]] thick, and the two are separated by a gap of 10-20 nm, called the [[intermembrane space]]. The outer membrane is permeable to most [[ions]] and [[metabolite]]s, but the [[inner membrane]] is highly specialised with [[transport protein]]s. Carbohydrates are transported across the outer membrane by a [[triose phosphate translocator]]. One or two additional membranes may enclose chloroplasts in [[algae]].
'''[[Chloroplast]]s''' contain several important [[biological membrane|membranes]], vital for their function. Like [[mitochondria]], chloroplasts have a double-membrane envelope, called the '''chloroplast envelope'''. Each membrane is a [[lipid bilayer]] that is between 6 and 8 [[nanometre|nm]] thick. The lipid composition of the outer membrane has been found to be 48% [[phospholipids]], 46% [[galactolipids]] and 6% [[sulfolipids]], while the inner membrane has been found to contain 16% [[phospholipids]], 79% [[galactolipids]] and 5% [[sulfolipids]] in spinach chloroplasts.<ref>Block, M. A., A. J. Dorne, J. Joyard, and R. Douce. “Preparation and Characterization of Membrane Fractions Enriched in Outer and Inner Envelope Membranes from Spinach Chloroplasts. II. Biochemical Characterization.” Journal of Biological Chemistry 258, no. 21 (November 10, 1983): 13281–13286.</ref> The outer membrane is permeable to most [[ions]] and [[metabolite]]s, but the [[inner membrane]] is highly specialised with [[transport protein]]s. Carbohydrates are transported across the outer membrane by a [[triose phosphate translocator]]. The two envelope membranes are separated by a gap of 10-20&nbsp;nm, called the [[intermembrane space]]. One or two additional membranes may enclose chloroplasts in [[algae]].


The origin of chloroplasts is now largely accepted by the botany community as occurring via [[endosymbiosis]] on an ancestral basis with the engulfment of photosynthetic bacterium within the eukaryotic cell. Over millions of years the endosymbiotic cyanobacterium evolved structurally and functionally, retaining its own DNA and the ability to divide by binary fission (not mitotically) but giving up its autonomy by the transfer of some of its genes to the nuclear genome.
The origin of chloroplasts is now largely accepted by the botany community as occurring via [[endosymbiosis]] on an ancestral basis with the engulfment of photosynthetic bacterium within the eukaryotic cell. Over millions of years the endosymbiotic cyanobacterium evolved structurally and functionally, retaining its own DNA and the ability to divide by binary fission (not mitotically) but giving up its autonomy by the transfer of some of its genes to the nuclear genome.
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Experiments have shown that the pH within the stroma is about 7.8, while that of the lumen of the thylakoid is 5. This corresponds to a six-hundredfold difference in concentration of H+ ions. The H+ ions pass down through the ATP-synthase catalytic gate. This chemiosmotic phenomenon occurs in mitochondria.
Experiments have shown that the pH within the stroma is about 7.8, while that of the lumen of the thylakoid is 5. This corresponds to a six-hundredfold difference in concentration of H+ ions. The H+ ions pass down through the ATP-synthase catalytic gate. This chemiosmotic phenomenon occurs in mitochondria.

==References==
{{Reflist}}


{{DEFAULTSORT:Chloroplast Membrane}}
{{DEFAULTSORT:Chloroplast Membrane}}

Revision as of 18:47, 6 April 2013

The simplified internal structure of a chloroplast

Chloroplasts contain several important membranes, vital for their function. Like mitochondria, chloroplasts have a double-membrane envelope, called the chloroplast envelope. Each membrane is a lipid bilayer that is between 6 and 8 nm thick. The lipid composition of the outer membrane has been found to be 48% phospholipids, 46% galactolipids and 6% sulfolipids, while the inner membrane has been found to contain 16% phospholipids, 79% galactolipids and 5% sulfolipids in spinach chloroplasts.[1] The outer membrane is permeable to most ions and metabolites, but the inner membrane is highly specialised with transport proteins. Carbohydrates are transported across the outer membrane by a triose phosphate translocator. The two envelope membranes are separated by a gap of 10-20 nm, called the intermembrane space. One or two additional membranes may enclose chloroplasts in algae.

The origin of chloroplasts is now largely accepted by the botany community as occurring via endosymbiosis on an ancestral basis with the engulfment of photosynthetic bacterium within the eukaryotic cell. Over millions of years the endosymbiotic cyanobacterium evolved structurally and functionally, retaining its own DNA and the ability to divide by binary fission (not mitotically) but giving up its autonomy by the transfer of some of its genes to the nuclear genome.

Internal parts

Within the inner membrane, in the region called the stroma, there is a system of interconnecting flattened membrane compartments, called the thylakoids. These are the sites of light absorption and ATP synthesis, and contain many proteins, including those involved in the electron transport chain. Photosenthetics pigments such as chlorophylls a,b and c some others e.g. xanthophylls, carotenoids, phycobilins are also embedded within the granum membrane. With exception of chlorophyll a, all the other associated pigments are "accessory" and transfer energy to the reaction centers, Photosytems I and II.

Functions of thylakoids

The membranes of the thylakoid contain photosystems I and II which harvest solar energy to excite electrons which travel down the electron transport chain. This exergonic fall in potential energy along the way is used to draw (not pump!) H+ ions from the lumen of the thylakoid into the cytosol of a cyanobacterium or the stroma of a chloroplast. A steep H+ gradient is formed, which allows chemiosmosis to occur, where the thylakoid, transmenbrane ATP-synthase serves a dual function as a "gate" or channel for H+ ions and a catalytic site for the formation of ATP from ADP + a P0-4 ion.

Experiments have shown that the pH within the stroma is about 7.8, while that of the lumen of the thylakoid is 5. This corresponds to a six-hundredfold difference in concentration of H+ ions. The H+ ions pass down through the ATP-synthase catalytic gate. This chemiosmotic phenomenon occurs in mitochondria.

References

  1. ^ Block, M. A., A. J. Dorne, J. Joyard, and R. Douce. “Preparation and Characterization of Membrane Fractions Enriched in Outer and Inner Envelope Membranes from Spinach Chloroplasts. II. Biochemical Characterization.” Journal of Biological Chemistry 258, no. 21 (November 10, 1983): 13281–13286.