by Nick Lane
In terms of the traditional account of life on our planet, the difficulty and investment required to split water and produce oxygen is a Darwinian paradox. The usual solution presented is selective pressure. Perhaps, for example, the stocks of hydrogen sulphide and dissolved iron salts eventually became depleted, putting life under pressure to adapt to an alternative, such as water. Perhaps, but on the face of it there is a difficulty here — the argument is circular. For the large geochemical stocks of hydrogen sulphide and iron to have become depleted in this way, they
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must have been oxidized by something, and the most likely, if not the only, candidate for oxidation on this scale is oxygen itself. The trouble is that there was no free oxygen before photosynthesis. Only photosynthesis can produce free molecular oxygen (O2) on the scale required. Thus, it seems that the only way to generate enough selective pressure for the evolution of photosynthesis is through the action of photosynthesis.
This argument is not just circular, it is also demonstrably false. We know from biomarkers diagnostic of cyanobacteria that oxygenic photosynthesis evolved more than 2.7 billion years ago. Despite this early evolution, we know that iron was still being precipitated from the oceans in vast banded iron formations a billion years later (Chapter 3). In no sense were oceanic iron salts depleted. Similarly, stagnant conditions, in which deep ocean waters are saturated with hydrogen sulphide, seem to have persisted until the time of the first large animals, the Vendobionts, and recur sporadically even today (Chapter 4). When these dates are taken together, we are forced to conclude that oxygenic photosynthesis evolved before the exhaustion of iron and hydrogen sulphide, at least on a global scale.
Why, and how, then, did oxygenic photosynthesis evolve? In the light of the last chapter, you may have guessed the answer already. There is good circumstantial evidence that oxidative stress, produced by solar radiation as on Mars (see Chapter 6, page 129), lies behind the evolution of photosynthesis on the Earth. The details are fascinating but also reveal just how deeply rooted is our resistance to oxygen toxicity: part and parcel, it seems, of the earliest known life on Earth. The earliest known bacteria did not produce oxygen by photosynthesis, but they could breathe oxygen — in other words they could apparently generate energy from oxygen-requiring respiration before there was any free oxygen in the air.
To understand how this could be, and why it is relevant to our health today, we need to look first at how photosynthesis works, and how it came to evolve.
Of the different types of photosynthesis carried out by living organisms, only the familiar oxygenic form practised by plants, algae and cyanobacteria generates oxygen. All other forms (collectively known as anoxygenic photosynthesis) do not produce oxygen and pre-date the more sophisticated oxygenic form. Despite our anthropocentric interest in
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oxygen, plants are not much concerned with the gas — what they need from photosynthesis is energy and hydrogen atoms. The different forms of photosynthesis are united only in that they all use light energy to make chemical energy (in the form of ATP) needed to cobble hydrogen onto carbon dioxide to form sugars. They differ in the source of the hydrogen, which might come from water, hydrogen sulphide or iron salts, or indeed any other chemical with hydrogen attached.
Overall, plant photosynthesis converts carbon dioxide (CO2) from the air into simple organic molecules such as sugars (general formula CH2O). These are subsequently burnt by the plant in its mitochondria (see Chapter 3) to produce more ATP, and also converted into the wealth of carbohydrates, lipids, proteins and nucleic acids that make up life. We met the enzyme that cobbles hydrogen onto carbon dioxide in Chapter 5
— Rubisco, the most abundant enzyme on the planet. But Rubisco needs to be spoon-fed with its raw materials — hydrogen and carbon dioxide.
Carbon dioxide comes from the air, or is dissolved in the oceans, so that is easy. Hydrogen, on the other hand, is not readily available — it reacts quickly (especially with oxygen to form water) and is so light that it can evaporate away into outer space. Hydrogen therefore needs a dedicated supply system of its own. This is, in fact, the key to photosynthesis, but for many years the lock resisted picking. Ironically, the mechanism only became clear when researchers finally understood where the oxygen waste came from.
In oxygenic photosynthesis, the hydrogen can only come from water, but the source of the oxygen is ambiguous. If we look at the overall chemical equation for photosynthesis, we see that it could come from either carbon dioxide or water:
CO2 + 2H2O 씮 (CH2O) + H2O + O2
At first, scientists guessed that the oxygen came from carbon dioxide — a perfectly reasonable and intuitive assumption, but quite wrong as it turned out. The fallacy was first exposed in 1931, when Cornelis van Niel showed that a strain of photosynthetic bacteria used carbon dioxide and hydrogen sulphide (H2S) to produce carbohydrate and sulphur in the presence of light— but did not give off oxygen:
CO2 + 2H2S 씮 (CH2O) + H2O + 2S
The chemical similarity between H2S and H2O led him to propose that in plants the oxygen might come not from carbon dioxide at all, but from
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water, and that the central trick of photosynthesis might be the same in both cases. The validity of this hypothesis was confirmed in 1937 by Robert Hill, who found that, if provided with iron ferricyanide (which does not contain oxygen) as an alternative to carbon dioxide, plants could continue to produce oxygen even if they could not actually grow.
Finally, in 1941, when a heavy isotope of oxygen (18O) became available, Samuel Ruben and Martin Kamen cultivated plants with water made with heavy oxygen. They found that the oxygen given off by the plants contained only the heavy isotope derived from water, proving conclusively that the oxygen came from water, not carbon dioxide.
In oxygenic photosynthesis, then, hydrogen atoms (or rather, the protons (H+) and electrons (e–) that constitute hydrogen atoms) are extracted from water, leaving the ‘husk’ — the oxygen — to be jettisoned into the air. The only advantage of water is its great abundance, for it is not easy to split in this way. The energy required to extract protons and electrons from water is much higher (nearly half as much again) than that needed to split hydrogen sulphide. Controlling this additional energy requires special ‘high-voltage’ molecular machinery, which had to evolve from the ‘low-voltage’ photosynthetic machinery previously used to split hydrogen sulphide. To understand how and why this voltage jump was made, we need to look at the structure and function of the machinery in a little more detail.
Whatever the source of hydrogen atoms — hydrogen sulphide or water —
the energy for their extraction is supplied by the electromagnetic rays that we know as sunlight. All electromagnetic rays, including light, are packaged into discreet units called photons, each of which has a fixed quantity of energy. The energy of a photon is related to the wavelength of the light, which is measured in nanometres (a billionth of a metre). The shorter the wavelength, the greater the energy. This means that ultraviolet photons (wavelength less than 400 nanometres) have more energy than red photons (wavelength of 600 to 700 nanometres), which have more energy than infrared photons (wavelength above 800 nanometres).
The interaction of light with any molecule always takes place at the level of the photon. In photosynthesis, chlorophyll is the molecule that absorbs photons. It cannot absorb any photon — it is constrained by the structure of its bonds to absorb photons with very particular quantities of energy. Plant chlorophyll absorbs photons of red light, with a wavelength of 680 nanometres. In contrast, the anoxygenic purple photosynthetic
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bacterium Rhodobacter sphaeroides has a different type of chlorophyll, which absorbs less-energetic infrared rays with a wavelength of 870
nanometres.1
When chlorophyll absorbs a photon, its internal bonds a
re energized.
The energetic vibrations force an electron from the molecule, leaving the chlorophyll short of one electron. Loss of an electron creates an unstable, reactive form of chlorophyll. However, the newly reactive molecule cannot simply take back its missing electron. That is snatched by a neighbouring protein and is whipped off down a chain of linked proteins, putting it beyond reach, like a rugby ball being passed across the field by a line of players.2 On the way, its energy is used to power the synthesis of ATP in a manner exactly analogous to that in mitochondrial respiration.
The theft of an electron is half way to stealing an entire hydrogen atom, as hydrogen consists of a single proton and a single electron. Little extra work is needed to steal the proton. Electrostatic rearrangements draw a positively charged proton (from water in the case of oxygenic photosynthesis) after the negatively charged electron. The proton and the electron are eventually reunited by Rubisco as a hydrogen atom in a sugar molecule.
What happens to the chlorophyll? Having lost an electron, it becomes far more reactive, and will snatch an electron from the nearest suitable source. Reactive chlorophyll is constrained in the same way as a mediaeval dragon which is fed with virgins to stop it ravaging the neigh-bourhood. The source of suitable virgins — electrons in the case of chlorophyll — includes any plentiful sacrificial chemical, such as water, hydrogen sulphide or iron. Devouring an electron settles the chlorophyll back into its normal equable state, at least until another photon sets the whole cycle in motion again.
1 Because plants absorb large amounts of red light, and reflect back more blue and yellow light, they appear green to us. In fact, chlorophylls are not the only light-absorbing molecules in plants. They are coupled with other pigments, such as carotenoids, which can absorb light of different wavelengths and transfer it to chlorophyll. It is the overall absorption spectrum of all these pigments operating together that gives plants their green colour.
2 Electrons pass along a gradient of electrochemical potential, from compounds with a low demand for electrons (low redox potential) to compounds with a high demand for electrons (high redox potential). ‘Electron-transport chains’ comprise strings of proteins and other electron-transfer molecules linked together in the order of their electrochemical potential.
Electrons usually pass smoothly down the chain from one end to the other, although sometimes they are poached by oxygen to produce superoxide radicals. At a certain step in the photosynthetic chain, the transfer of electrons from one molecule to another provides sufficient energy to power the manufacture of ATP.
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Which electron donor is used in photosynthesis — hydrogen sulphide, iron or water — ultimately depends on the energy of the photons that are absorbed by the chlorophyll. In the case of purple bacteria, their chlorophyll can only absorb low-energy infrared rays. This provides enough energy to extract electrons from hydrogen sulphide and iron, but not from water. To extract electrons from water requires extra energy, which must be acquired from higher-energy photons. To do this requires a change in the structure of chlorophyll, so it can absorb red-light photons instead of infrared light.
The evolutionary question is this: why did the structure of chlorophyll change, allowing it to absorb red light and split water, when the existing chlorophyll of purple bacteria could already extract electrons from hydrogen sulphide and iron salts, which were plentiful in the ancient oceans? More specifically, what environmental pressure could have led to the evolution of a new and more potent chlorophyll, capable of oxidizing water and much else in the cell, when the old chlorophyll was less reactive and less dangerous — and yet still sufficiently strong to oxidize hydrogen sulphide?
Technically, the answers to these questions are surprisingly simple.
According to Robert Blankenship of Arizona State University and Hyman Hartman, of the Institute for Advanced Studies in Biology at Berkeley, California, tiny changes in the structure of bacterial chlorophylls can lead to large shifts in their absorption properties. Two small changes to the structure of bacteriochlorophyll a (which absorbs at 870 nm) are all that it takes to generate chlorophyll d, which absorbs at 716 nanometres. In 1996, an article in Nature by Hideaki Miyashita and colleagues of the Marine Biotechnology Institute in Kamaishi, Japan, reported that chlorophyll d is the main photosynthetic pigment in a bacterium called Acaryochloris marina, which splits water to generate oxygen. Thus, an intermediate between bacteriochlorophyll and plant chlorophyll is not only plausible: it actually exists. From chlorophyll d another trifling change is all that is required to produce chlorophyll a, the principal pigment in plants, algae and cyanobacteria, which absorbs light at 680 nanometres.
Technically, then, the evolutionary steps required to get from bacteriochlorophyll to plant chlorophyll are simply achieved. The question remains, why? A chlorophyll that absorbs light at 680 nanometres is less good at absorbing light at 870 nanometres. It is therefore less efficient at splitting hydrogen sulphide, and so bacteria carrying it are at a competitive disadvantage compared with the bacteria that kept their original
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chlorophyll. Even worse, switching chlorophylls to split water poses the problem of what to do with the toxic oxygen waste, as well as any leaking free-radical intermediates — the same as those produced by radiation.
Without foresight, how did life manage to cope with its dangerous new invention?
Chlorophyll extracts electrons from water one at a time. To generate oxygen from water, it must absorb four photons and lose four electrons in succession, each time drawing an electron from one of two water molecules.3 The overall water-splitting reaction is:
2H2O 씮 O2 + 4H+ + 4 e–
Only in the final stage is oxygen released. The rate at which chlorophyll extracts electrons depends on how quickly the photons are absorbed. As the successive steps cannot take place instantly, a series of potentially reactive free-radical intermediates must be produced, if only transiently.
For plants, this whole system is precarious in the extreme. Reactive oxygen intermediates are produced from water as it is stripped of electrons one by one to form oxygen. Some of these reactive intermediates might escape from the reaction site to devastate nearby molecules. Even if they don’t escape, in the final step molecular oxygen is released into the cell in large quantities. Inside a modern plant leaf the oxygen concentration can reach three times atmospheric levels. Tiny cyanobacteria pollute themselves and their immediate surroundings in a similar fashion. This would have happened even in ancient times before there was any oxygen in the surrounding air. Some of this excess oxygen inevitably steals stray electrons to form superoxide radicals. The risks are huge. Chaos could break out at any moment. The closest analogy is a nuclear power station.
If the reactors are sealed properly it is safe enough, but if a leak develops we face a disaster on the scale of Chernobyl. In both nuclear power and oxygenic photosynthesis the safety margins are slim, but the potential benefits — unlimited energy — are huge.
3 As usual, it is a little more complicated than this. In fact, a second light-activated centre is required for oxygenic photosynthesis. Neither reaction centre alone can bridge the wide chemical gulf between stealing electrons from water and attaching them to carbon dioxide
— so the two centres must work together. The centres are coupled, essentially in series, in what is known as a Z scheme, and each absorbs four photons in a single cycle. To produce one molecule of oxygen therefore requires eight photons of light.
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If photosynthesis is to work at all, the reactive intermediates from water must be sealed inside a structure that immobilizes them, preventing them from escaping before oxygen is released. Needless to say, they are sealed in such a cage, this is how photosynthesis works. The cage is made of proteins and is called the oxygen-evolving complex (or sometimes the water-splitting enzyme). Water is bou
nd tightly inside the protein cage while the electrons are extracted one at a time. But this is no ordinary cage. Its structure conceals a secret that is much older than the hills, which transports us back to the time before oxygenic photosynthesis evolved, to a time more than 2.7 billion years ago, before there was any oxygen in the atmosphere. This structure is the key to life on Earth, for without it the Earth would have remained as sterile as Mars.
The structure of the oxygen-evolving complex is very similar to that of an antioxidant enzyme called catalase. In fact, the oxygen-evolving complex looks as if it evolved from two catalase enzymes lashed together.4
If so, then catalase must have evolved before the oxygen-evolving complex. If so, the chronology must be as follows. Catalase evolved on the early Earth, in an atmosphere devoid of oxygen. One day, two catalase molecules became bound together to form a cage that enabled the safe splitting of water: the oxygen-evolving complex. This cage allowed the evolution of oxygenic photosynthesis. As a result, the atmosphere filled with oxygen. Life was put under serious oxidative stress. Luckily it could cope: it already had at least one antioxidant enzyme that could to protect it — catalase. How convenient! But wait a moment. If catalase came before photosynthesis, then even if there was no atmospheric oxygen, there must have been oxidative stress. Is this plausible? To answer this question, we must take a look at how catalase works.
4 The evidence is not compelling, but is certainly intriguing. First, there is a broad similarity in reaction mechanisms. Both catalase and the oxygen-evolving complex bind two identical molecules (either 2H2O2 or 2H2O), which are then reacted together to generate oxygen, via a strikingly similar sequence of steps. Second, both contain clusters of manganese atoms at their core. Hyman Hartman and others have noted that the manganese core of catalase is structurally very similar to half that of the oxygen-evolving complex, implying that the latter may have evolved by the lashing together of two catalase units. However, it is possible that the structural similarities between catalase and the oxygen-evolving complex are no more than coincidence, or a case of convergent evolution towards a similar endpoint, like the development of wings from very different structures in insects, birds and bats. Even if the similarity is authentic evidence of genetic relatedness, we cannot rule out the possibility that catalase evolved from the oxygen-evolving complex rather than the other way round.