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The energy of P680 + is used in two steps to split a water molecule into 2H + + 1/2 O 2 + 2e-(photolysis or light-splitting). An electron from the water molecule reduces P680 + back to P680, while the H + and oxygen are released.
Location of the psa genes in the chloroplast genome of Arabidopsis thaliana.The 21 protein-coding genes involved in photosynthesis are displayed as green boxes. Photosystem I (PSI, or plastocyanin–ferredoxin oxidoreductase) is one of two photosystems in the photosynthetic light reactions of algae, plants, and cyanobacteria.
In biochemistry, a polymerase is an enzyme (EC 2.7.7.6/7/19/48/49) that synthesizes long chains of polymers or nucleic acids. DNA polymerase and RNA polymerase are used to assemble DNA and RNA molecules, respectively, by copying a DNA template strand using base-pairing interactions or RNA by half ladder replication.
The polymerase is a monomeric protein with two distinct functional domains. Site-directed mutagenesis experiments support the proposition that this protein displays a structural and functional similarity to the Klenow fragment of the Escherichia coli Polymerase I enzyme; [3] it comprises a C-terminal polymerase domain and a spatially separated N-terminal domain with a 3'-5' exonuclease activity.
Calvin cycle step 1 (black circles represent carbon atoms) Calvin cycle steps 2 and 3 combined. The enzyme RuBisCO catalyses the carboxylation of ribulose-1,5-bisphosphate, RuBP, a 5-carbon compound, by carbon dioxide (a total of 6 carbons) in a two-step reaction. [6] The product of the first step is enediol-enzyme complex that can capture CO 2 ...
DNA polymerase III synthesizes base pairs at a rate of around 1000 nucleotides per second. [3] DNA Pol III activity begins after strand separation at the origin of replication. Because DNA synthesis cannot start de novo, an RNA primer, complementary to part of the single-stranded DNA, is synthesized by primase (an RNA polymerase): [citation ...
DNA polymerase's ability to slide along the DNA template allows increased processivity. There is a dramatic increase in processivity at the replication fork. This increase is facilitated by the DNA polymerase's association with proteins known as the sliding DNA clamp. The clamps are multiple protein subunits associated in the shape of a ring.
Loads DNA polymerase α onto chromatin together with CMG complex on the lagging strand. Also known as Ctf4 in budding yeast. Cdc45: Required for initiation and elongation steps of DNA replication. A part of the Mcm2-7 helicase complex. Required after pre-RC step for loading of various proteins for initiation and elongation. Cdc45-Mcm-GINS (CMG ...