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| This weeks hot offer 
  24: Series 5 
 In association with Amazon.co.uk £26.97
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| Contents
 
 
  Plant photosynthesis 
  Photosynthesis in algae and bacteria 
  Molecular production 
  Discovery 
  Bioenergetics of photosynthesis 
  Factors affecting photosynthesis 
  In detail 
 
 
 
  Plant photosynthesis - Contents 
 Plants are  photoautotrophs, which means they are able to synthesize food directly from inorganic compounds using light energy, instead of eating other organisms or relying on material derived from them. This is distinct from  chemoautotrophs that do not depend on light energy, but use energy from inorganic compounds.The energy for photosynthesis ultimately comes from absorbed photons and involves a reducing agent, which is water in the case of plants, releasing oxygen as a waste product. The light energy is converted to chemical energy, in the form of  ATP and  NADPH, using the  light-dependent reactions and is then available for  carbon fixation. Most notably plants use the chemical energy to fix carbon dioxide into  carbohydrates and other organic compounds through  light-independent reactions. The overall equation for photosynthesis in green plants is:
 
       n CO2 + 2n H2O + light energy → (CH2O)n + n O2 + n H2O Where n is defined according to the structure of the resulting carbohydrate. However,  hexose sugars and  starch are the primary products, so the following generalised equation is often used to represent photosynthesis:
 
       More specifically, photosynthetic reactions usually produces an intermediate product, which is then converted to the final hexose carbohydrate products. These carbohydrate products are then variously used to form other organic compounds, such as the building material  cellulose, as precursors for lipid and  amino acid biosynthesis or as a fuel in  cellular respiration. The latter not only occurs in plants, but also in animals when the energy from plants get passed through a  food chain. In general outline, cellular respiration is the opposite of photosynthesis: glucose and other compounds are oxidised to produce carbon dioxide, water, and chemical energy. However, both processes actually take place through a different sequence of reactions and in different cellular compartments.Plants capture light primarily using the pigment chlorophyll, which is the reason that most plants have a green colour. The function of chlorophyll is often supported by other  accessory pigments such as  carotenoids and  xanthophylls. Both chlorophyll and accessory pigments are contained in  organelles (compartments within the  cell) called chloroplasts. Although all cells in the green parts of a plant have chloroplasts, most of the energy is captured in the leaves. The cells in the interior tissues of a leaf, called the  mesophyll, contain about half a million chloroplasts for every square millimeter of leaf. The surface of the leaf is uniformly coated with a water-resistant,  waxy  cuticle, that protects the leaf from excessive  evaporation of water as well as decreasing the absorption of ultraviolet or  blue  light to reduce  heating. The transparent, colourless  epidermis layer allows light to pass through to the  palisade mesophyll cells where most of the photosynthesis takes place.6 CO2 + 6 H2O + light energy → C6H12O6 + 6 O2 
 
 
  Photosynthesis in algae and bacteria - Contents 
 Algae range from multicellular forms like  kelp to  microscopic, single-celled organisms. Although they are not as complex as land plants, photosynthesis takes place biochemically the same way. Like plants, algae have chloroplasts and chlorophyll, but various accessory pigments are present in some algae such as phycoerythrin in red algae (rhodophytes) , resulting in a wide variety of colours. All algae produce oxygen, and many are autotrophic. However, some are  heterotrophic, relying on materials produced by other organisms.Photosynthetic bacteria do not have chloroplasts (or any membrane-bound organelles), instead, photosynthesis takes place directly within the cell. Cyanobacteria contain thylakoid membranes very similar to those in chloroplasts and are the only prokaryotes that perform oxygen-generating photosynthesis, in fact chloroplasts are now considered to have  evolved from an  endosymbiotic bacterium, which was also an ancestor of and later gave rise to cyanobacterium. The other photosynthetic bacteria have a variety of different pigments, called  bacteriochlorophylls, and do not produce oxygen. Some bacteria such as Chromatium, oxidize hydrogen sulfide instead of water for photosynthesis, producing sulfur as waste.
 
 
 
  Molecular production - Contents 
 
 
 Light to chemical energy
 
 
       
          A photosystem: a light-harvesting cluster of photosynthetic pigments in a chloroplast thylakoid membrane. 
       The light energy is converted to chemical energy using the  light-dependent reactions. The products of the light dependent reactions are  ATP from photophosphorylation and  NADPH from photoreduction. Both are then utilized as an energy source for the  light-independent reactions.
          The 'Z-scheme' of electron flow in light-dependent reactions. Z schemeIn plants, the light-dependent reactions occur in the  thylakoid membranes of the chloroplasts and use light energy to synthesize ATP and NADPH. The photons are captured in the  antenna complexes of  photosystem I and II by chlorophyll and  accessory pigments (see diagram at right). When a chorophyll a molecule at a photosystem's reaction center absorbs energy, an electron is excited and transferred to an electron-acceptor molecule through a process called  Photoinduced charge separation. These electrons are shuttled through an  electron transport chain that initially functions to generate a  chemiosmotic potential across the membrane, the so called Z-scheme shown in the diagram. An  ATP synthase enzyme uses the chemiosmotic potential to make ATP during photophosphorylation while  NADPH is a product of the terminal  redox reaction in the Z-scheme.Water photolysisThe NADPH is the main  reducing agent in chloroplasts, providing a source of energetic electrons to other reactions. Its production leaves chlorophyll with a deficit of electrons (oxidized), which must be obtained from some other reducing agent. The excited electrons lost from chlorophyll in photosystem I are replaced from the electron transport chain by  plastocyanin. However, since photosystem II includes the first steps of the Z-scheme, an external source of electrons is required to reduce its oxidized chlorophyll a molecules. This role is played by water during a reaction known as  photolysis and results in water being split to give electrons, oxygen and hydrogen ions. Photosystem II is the only known biological  enzyme that carries out this oxidation of water. Initially, the hydrogen ions from photolysis contribute to the chemiosmotic potential but eventually they combine with the  hydrogen carrier molecule NADP+ to form  NADPH. Oxygen is a waste product of photosynthesis but it has a vital role for all organisms that use it for cellular respiration.Oxygen and photosynthesisWith respect to oxygen and photosynthesis, there are two important concepts.
       Plant and algal cells also use oxygen for cellular respiration, although they have a net output of oxygen since much more is produced during photosynthesis. 
       Oxygen is a product of the photolysis reaction not the fixation of carbon dioxide during the light-independent reactions. Consequently, the source of oxygen during photosynthesis is water, NOT carbon dioxide. Bacterial variationsThe concept that oxygen production is not directly associated with the fixation of carbon dioxide was first proposed by  Cornelis Bernadus van Neil in the 1930s, who studied photosynthetic bacteria. Aside from the  cyanobacteria, bacteria only have one photosystem and use reducing agents other than water. They get electrons from a variety of different inorganic chemicals including  sulfide or hydrogen, so for most of these bacteria oxygen is not produced.Others, such as the halophiles (an Archeae) produced so called purple membranes where the bacteriorhodopsin could harvest light and produce energy. The purple membranes was one of the first to be used to demonstrate the chemiosmotic theory: light hit the membranes and the pH of the solution that contained the purple membranes dropped as protons were pumping out of the membrane.
 Carbon fixation
 The  fixation of carbon dioxide is a  light-independent process in which carbon dioxide combines with a five-carbon sugar,  ribulose bisphosphate (RuBP), to give two molecules of a three-carbon compound,  glycerate 3-phosphate (GP). This compound is also sometimes known as 3-phosphoglycerate (PGA). GP, in the presence of  ATP and  NADPH from the light-dependent stages, is reduced to  glyceraldehyde 3-phosphate (G3P). This product is also referred to as 3-phosphoglyceraldehyde ( PGAL) or even as triose phosphate (a  three-carbon sugar). This is the point at which  carbohydrates are produced during photosynthesis. Some of the  triose phosphates condense to form  hexose phosphates,  sucrose,  starch and  cellulose or are converted to acetylcoenzyme A to make  amino acids and  lipids. Others go on to regenerate RuBP so the process can continue (see Calvin cycle).
 
 
 
  Discovery - Contents 
 Although some of the steps in photosynthesis are still not completely understood, the overall photosynthetic equation has been known since the  1800s.
        Jan van Helmont began the research of the process in the mid-1600s when he carefully measured the  mass of the soil used by a plant and the mass of the plant as it grew. After noticing that the soil mass changed very little, he hypothesized that the mass of the growing plant must come from the water, the only substance he added to the potted plant. This was a partially accurate hypothesis - much of the gained mass also comes from carbon dioxide as well as water. However, this was a signalling point to the idea that the bulk of a plant's  biomass comes from the inputs of photosynthesis, not the soil itself.
        Joseph Priestley, a chemist and minister, discovered that when he isolated a volume of air under an inverted jar, and burned a candle in it, the candle would burn out very quickly, much before it ran out of wax. He further discovered that a mouse could similarly "injure" air. He then showed that the air that had been "injured" by the candle and the mouse could be restored by a plant.In  1778,  Jan Ingenhousz, court physician to the Austrian Empress, repeated Priestley's experiments. He discovered that it was the influence of sun and light on the plant that could cause it to rescue a mouse in a matter of hours.In  1796,  Jean Senebier, a French pastor, showed that CO2 was the "fixed" or "injured" air and that it was taken up by plants in photosynthesis. Soon afterwards,  Nicolas-Théodore de Saussure showed that the increase in mass of the plant as it grows could not be due only to uptake of CO2, but also to the incorporation of water. Thus the basic reaction by which photosynthesis is used to produce food (such as glucose) was outlined.Modern scientists built on the foundation of knowledge from those scientists centuries ago and were able to discover many things.
        Cornelius Van Niel made key discoveries explaining the chemistry of photosynthesis. By studying  purple sulfur bacteria and green bacteria he was the first scientist to demonstrate that photosynthesis is a light-dependent  redox reaction, in which hydrogen reduces carbon dioxide.Further experiments to prove that the oxygen developed during the photosynthesis of green plants came from water, were performed by  Robert Hill in  1937 and  1939. He showed that isolated chloroplasts give off oxygen in the presence of unnatural reducing agents like iron oxalate,  ferricyanide or  benzoquinone after exposure to light. The Hill reaction is as follows:
 
       where A is the electron acceptor. Therefore, in light the electron acceptor is reduced and oxygen is evolved.
        Samuel Ruben and  Martin Camen used radioactive isotopes to determine that the oxygen liberated in photosynthesis came from the water.
        Melvin Calvin and his partner Benson were able to puzzle out each stage in the dark or light-independent phase of photosynthesis, known as the Calvin cycle.A  Nobel Prize winning scientist,  Rudolph A. Marcus, was able to discover the function and significance of the electron transport chain.2 H2O + 2 A + (light, chloroplasts) → 2 AH2 + O2 
 
 
  Bioenergetics of photosynthesis - Contents 
 Photosynthesis is a physiological phenomenon that converts  solar energy into photochemical energy. This physiological phenomenon may be described thermodynamically in terms of changes in  energy,  entropy and  free energy. The  energetics of photosynthesis, driven by light, causes a change in entropy that in turn yields a usable source of energy for the plant.The following  chemical equation summarizes the products and reactants of photosynthesis in the typical green photosynthesizing plant:
 CO2 + H2O → O2 + (CH2O) + 112  kcal/ mol CO2
 On earth, there are two sources of free crap: light energy from the sun, and terrestrial sources, including volcanoes, hot springs and radioactivity of certain elements. The biochemical value of electromagnetic radiation has led plants to use the free energy from the sun in particular.  Visible light, which is used specifically by green plants to photosynthesize, may result in the formation of electronically excited states of certain substances called  pigments (Gregory). For example, Chl a is a pigment which acts as a catalyst, converting solar energy into photochemical energy that is necessary for photosynthesis (Govindjee).With the presence of solar energy, the plant has a usable source of energy, which is termed the free energy (G) of the system. However, thermal energy is not completely interconvertible, which means that the character of the solar energy may lead to the limited convertibility of it into forms that may be used by the plant. This relates back to the work of  Josiah Willard Gibbs: the change in free energy (ΔrG) is related to both the change in entropy (ΔrS) and the change in  enthalpy (ΔrH) of the system (Rabinowitch).
 Gibbs free energy equation: ΔrG = ΔrH – TΔrS... where ΔH is enthalpy, ΔS is entropy, and T is temperature.
        Steelmans free energy equation: ΔtG × Δ<super>lH – SΔn<super>12S = nx</super>±12.332Past experiments have shown that the total energy produced by photosynthesis is 112 kcal/mol. However in the experiment, the free energy due to light was 120 kcal/mol. An overall loss of 8 kcal/mol was due to entropy, as described by Gibbs equation (Gonindjee). In other words, since the usable energy of the system is related directly to the entropy and temperature of the system, a smaller amount of  thermal energy is available for conversion into usable forms of energy (including mechanical and chemical) when entropy is great (Rabinowitch). This concept relates back to the  second law of thermodynamics in that an increase in entropy is needed to convert light energy into energy suitable for the plant.Overall, in conjunction with the  oxidation-reduction reaction nature of the photosynthesis equation, and the interrelationships between entropy and enthalpy, energy in a usable form will be produced by the photosynthesizing green plant.
 
 
 
  Factors affecting photosynthesis - Contents 
 There are three main factors affecting photosynthesis and several corollary factors. The three main are:
 
       Light  irradiance and  wavelengthCarbon dioxide concentration
         Temperature 
 Light intensity (Irradiance), wavelength and temperature
 In the early 1900s  P.P. Blackman investigated the effects of light intensity ( irradiance) and temperature on the rate of photosynthesis. At constant temperature the rate of photosynthesis varies with irradiance, initially increasing as the irradiance increases. However at higher irradiance this relationship no longer holds and the rate of photosynthesis reaches a plateau. The effect on the rate of photosynthesis of varying the temperature at constant irradiance can be seen in image to the left. At high irradiance the rate of photosynthesis increases as the temperature is increased over a limited range. At low irradiance, increasing the temperature has little effect on the rate of photosynthesis. These two experiments illustrate vital points: firstly, from  research it is known that  photochemical reactions are not generally affected by  temperature. However, these experiments clearly show that temperature affects the rate of photosynthesis, so there must be two sets of reactions in the full process of photosynthesis. These are of course the  light-dependent 'photochemical' stage and the  light-independent, temperature-dependent stage. Secondly, Blackman's experiments illustrate the concept of  limiting factors. Another limiting factor is the wavelength of light. Cyanobacteria which reside several metres underwater cannot receive the correct wavelengths required to cause photoinduced charge separation in conventional photosynthetic pigments. To combat this problem a series of proteins with different flourescent pigments surround the reaction centre. This unit is called a  phycobilisome.
 
 Carbon dioxide
 As carbon dioxide concentrations rise, the rate at which sugars are made by the light-independent reactions increases until limited by other factors. One reason for this is that  RuBisCO, the enzyme fixing the carbon dioxide in the light-dependent reactions, has a binding affinity for both carbon dioxide and oxygen. Thus, an increase in the concentration of carbon dioxide increases the probability of RuBisCO fixing carbon dioxide instead of oxygen.A reduced RuBisCO oxygenase activity is advantageous to plants for several reasons.
 
       One product of oxygenase activity is  phosphoglycolate (2 carbon) instead of  3-phosphoglycerate (3 carbon). Phosphoglycolate cannot be metabolised by the Calvin cycle and represents carbon lost from the cycle. A high oxygenase activity, therefore, drains the sugars that are required to recycle ribulose 5-bisphosphate and for the continuation of the Calvin cycle.Phosphoglycolate is quickly metabolised to glycolate that is toxic to a plant at a high concentration; it inhibits photosynthesis.Salvaging glycolate is an energetically expensive process that uses the glycolate pathway and only 75% of the carbon is returned to the Calvin cycle as 3-phosphoglycerate. 
       
        
         A highly simplified summary is: 
       The salvaging pathway for the products of RuBisCO oxygenase activity is more commonly known as  photorespiration since it is characterised by light dependent oxygen consumption and the release of carbon dioxide.
        
         
          
           2 glycolate + ATP → 3-phophoglycerate + carbon dioxide + ADP +NH3 
 Corollary factors
 
 
       Amount of waterLeaf morphologyLeaf nitrogen contentMolecular carriers such as  NADP and  FAD 
 
 
  In detail - Contents 
 Metabolic pathways involved in photosynthesis:
 
       Photosynthesis is the process by which radiant energy is converted to chemical bond energy (ie. the macromolecule which we commonly refer to as GLUCOSE)
         Light-dependent reaction
         Light-independent reaction |  
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