structure and function of chloroplast Flashcards | Quizlet

(Photosynth prokaryotes lack chloroplasts, but, as you will see Chapter 25, they do have membranes that manner similar to the thylakoid membranes of chloroplasts.) Now that we have identified chloroplasts sites of photosynthesis in plants, we are ready to see these organelles convert the light energy absorbed chlorophyll to chemical energy.

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Thylakoid membranes, especially those of the grana, are the sites of the light reactions, whereas the Calvin cycle occurs in the stoma.

what is the function of thylakoid membranes

Antenna ComplexesThe prime function of chloroplast is absorption of light and that is executed by the thylakoid membrane mechanism.

Each of the four photosynthetic complexes contains numerous protein subunits, some of which are encoded by the chloroplast genome, whereas others are encoded by the nuclear genome (Table 1; Fig. 2). The two principal reaction center polypeptides of photosystems I and II are highly hydrophobic and contain 11 and 5 transmembrane a-helices, respectively, to which most of the redox cofactors and several chlorophylls are bound with an asymmetrical distribution across the thylakoid membrane. This asymmetry is crucial for the vectorial electron transport in the membrane.

Why would the stroma have a higher pH during photosynthesis

So we can summarize by saying that the photosynthetic plantstrap solar energy to form ATP and NADPH (Light Phase) and thenuse these as the energy source to make carbohydrates and otherbiomolecules from carbon dioxide and water (Dark Phase),simultaneously releasing oxygen in to the atmosphere. Thechemoheterotrophic animals reverse this process by using theoxygen to degrade the energy-rich organic products ofphotosynthesis to CO2 and water in order to generate ATP fortheir own synthesis of biomolecules.

Thylakoid membrane - definition of Thylakoid membrane …

A limiting factor is a factor that controls a process. Light intensity, temperature and carbon dioxide concentration are all factors which can control the rate of photosynthesis. Usually, only one of these factors will be the limiting factor in a plant at a certain time. This is the factor which is the furthest from its optimum level at a particular point in time. If we change the limiting factor the rate of photosynthesis will change but changes to the other factors will have no effect on the rate. If the levels of the limiting factor increase so that this factor is no longer the furthest from its optimum level, the limiting factor will change to the factor which is at that point in time, the furthest from its optimum level. For example, at night the limiting factor is likely to be the light intensity as this will be the furthest from its optimum level. During the day, the limiting factor is likely to switch to the temperature or the carbon dioxide concentration as the light intensity increases.

Chloroplast Structure and Function - Coloring

Two distinct RNA polymerases are present in the chloroplasts of higher plants. One is similar to its bacterial homologue, and its subunits are encoded by chloroplast genes. This enzyme transcribes primarily genes involved in photosynthesis, which are expressed at a high level. The second plastid RNA polymerase is nucleus-encoded and is required for expressing the nonphotosynthetic plastid functions necessary for plant growth (11). Many chloroplast genes are organized in large transcription units. These units are transcribed into large precursor transcripts, which then are processed into individual messenger RNA (mRNA) molecules. Chloroplasts contain RNA splicing systems, because several plastid genes contain introns, mostly group II and group I, which have a characteristic secondary structure (12). These introns have also been found in mitochondrial genes, and some of them are self-splicing. Splicing in the chloroplast is rather complex, as in the case of the psaA gene encoding one of the reaction center polypeptides of photosystem I in the green alga Chlamydomonas. This gene consists of three coding regions (exons) that are widely separated on the chloroplast genome and are flanked by group II intron sequences (13). They are transcribed individually, and maturation of the psaA mRNA depends on two trans-splicing reactions in which the separate transcripts of the three exons are spliced together. A particularly intriguing feature is that one of the introns is split into three parts (14). This has interesting evolutionary implications because it is thought that group II introns represent the precursors of nuclear introns and their associated splicing factors. In this view, the split chloroplast intron may represent an intermediate between group II and nuclear introns. The chloroplast genetic system has evolved at a rather slow rate and could have therefore maintained some ancient gene organization.