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The thylakoid membranes of higher plants are composed primarily of phospholipids [5] and galactolipids that are asymmetrically arranged along and across the membranes. [6] Thylakoid membranes are richer in galactolipids rather than phospholipids; also they predominantly consist of hexagonal phase II forming monogalacotosyl diglyceride lipid.
This process, called photorespiration, uses energy, but does not produce sugars. RuBisCO oxygenase activity is disadvantageous to plants for several reasons: One product of oxygenase activity is phosphoglycolate (2 carbon) instead of 3-phosphoglycerate (3 carbon). Phosphoglycolate cannot be metabolized by the Calvin-Benson cycle and represents ...
A C3 plant uses C3 carbon fixation, one of the three metabolic photosynthesis pathways which also include C4 and CAM (described below). These plants are called "C3" due to the three-carbon compound (3-Phosphoglyceric acid, or 3-PGA) produced by the CO 2 fixation mechanism in these plants.
C 4 plants have a competitive advantage over plants possessing the more common C 3 carbon fixation pathway under conditions of drought, high temperatures, and nitrogen or CO 2 limitation. When grown in the same environment, at 30 °C, C 3 grasses lose approximately 833 molecules of water per CO 2 molecule that is fixed, whereas C 4 grasses
Photosystem II (of cyanobacteria and green plants) is composed of around 20 subunits (depending on the organism) as well as other accessory, light-harvesting proteins. Each photosystem II contains at least 99 cofactors: 35 chlorophyll a, 12 beta-carotene , two pheophytin , two plastoquinone , two heme , one bicarbonate, 20 lipids, the Mn
This allows them to stack tightly, forming grana with many layers of tightly appressed membrane, called granal membrane, increasing stability and surface area for light capture. [148] In contrast, photosystem I and ATP synthase are large protein complexes which jut out into the stroma. They can't fit in the appressed granal membranes, and so ...
Photosystem I (PSI, or plastocyanin–ferredoxin oxidoreductase) is one of two photosystems in the photosynthetic light reactions of algae, plants, and cyanobacteria. Photosystem I [1] is an integral membrane protein complex that uses light energy to catalyze the transfer of electrons across the thylakoid membrane from plastocyanin to ferredoxin.
Hence, plants regulate the amount of this chlorophyll precursor. In angiosperms, this regulation is achieved at the step of aminolevulinic acid (ALA), one of the intermediate compounds in the biosynthesis pathway. Plants that are fed by ALA accumulate high and toxic levels of protochlorophyllide; so do the mutants with a damaged regulatory ...