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Encyclopedia of Evolution.pdf - Online Reading Center

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oth may have been a chemical wonderland, but it could<br />

not have included all the compounds and molecular structures<br />

found in the simplest <strong>of</strong> present-day microbes.”<br />

A particular problem has been in designing a “one-pot<br />

reaction” in which the scientist puts inorganic chemicals<br />

in and gets living cells out. In order to obtain the different<br />

molecules necessary for life, very different conditions <strong>of</strong><br />

acidity and temperature are needed. For example, freezing<br />

conditions are necessary to preserve adenine and guanine,<br />

while for cytosine and uracil warm evaporative conditions<br />

are needed. Biologist Robert Shapiro has been particularly<br />

eager to point out how implausible these prebiotic syntheses<br />

would have been, requiring an unbelievable configuration<br />

<strong>of</strong> heat and cold, salinity and purity, acidity and neutrality—a<br />

series <strong>of</strong> unlikely events occurring in just the right<br />

order to produce even a few <strong>of</strong> the chemical building blocks<br />

<strong>of</strong> life. The chemical simulations are, according to Simon<br />

Conway Morris, “…highly artificial, if not contrived.” The<br />

outcome <strong>of</strong> the syntheses depends strongly on the starting<br />

conditions. The reactions would not work at all in a neutral<br />

atmosphere, rather than a reducing atmosphere (see above).<br />

Stanley Miller used a continuous spark plug; but when brief,<br />

stronger blasts <strong>of</strong> electricity (which simulate lightning) were<br />

used, the results were disappointing. When the order <strong>of</strong> the<br />

glassware components changed, the results were different.<br />

Some experiments would not have worked without doubly<br />

purified water, available in chemical laboratories but not on<br />

the primitive Earth. So far, there has been little promise from<br />

one-pot reactions in explaining the origin <strong>of</strong> all <strong>of</strong> the chemicals<br />

<strong>of</strong> life, converging in one place at one time.<br />

6. Origin <strong>of</strong> “handedness” in biological molecules. Organic<br />

molecules can have left- v. right-handed mirror images,<br />

exactly the way human left and right hands are identical but<br />

opposite to one another. Organic molecules produced by<br />

nonliving processes are almost always chiral, an equal mixture<br />

<strong>of</strong> the two forms. However, proteins in organisms use<br />

left-handed amino acids and right-handed nucleic acids. A<br />

protein made <strong>of</strong> all left-handed, or all right-handed, amino<br />

acids is more stable than a protein made <strong>of</strong> a mixture. But,<br />

how did the preponderance <strong>of</strong> left-handed amino acids ever<br />

get started in the first place? There was great excitement<br />

when it was discovered that meteorites could have an excess<br />

<strong>of</strong> left-handed amino acids—but this excess was only 7–10<br />

percent. It has been suggested that ultraviolet light polarized<br />

the amino acids before the meteorites reached the Earth. It<br />

is still unclear whether this could have happened on the primordial<br />

Earth. It has been demonstrated that divalent cations<br />

(such as the calcium ion Ca ++ ) can produce an uneven<br />

mixture <strong>of</strong> the two forms <strong>of</strong> organic molecules.<br />

7. Synthesis <strong>of</strong> large molecules from small precursors. The<br />

production <strong>of</strong> small organic molecules may have been easy<br />

on the primordial Earth, just as in nebulae and comets, but<br />

how could small molecules have assembled into large ones,<br />

such as the proteins and nucleic acids needed by modern<br />

cells? Large molecules tend to dissociate into smaller ones<br />

in water. There are two processes that may have allowed<br />

the formation <strong>of</strong> large molecules on the primordial Earth:<br />

origin <strong>of</strong> life 0<br />

• Activated precursors. Regular amino acids do not polymerize<br />

into proteins in water very well, but amino acids in<br />

the amide form do. As biochemist James Ferris explains,<br />

carboxyanhydrides can form into protein-like molecules<br />

in water. When this happens, he points out, the resulting<br />

protein-like molecules form only the correct type<br />

<strong>of</strong> peptide bonds that characterize biological proteins;<br />

and, moreover, the resulting molecules, up to 10 amino<br />

acids in length, contain only left-handed components.<br />

• Adsorption on mineral surfaces. Small molecules bumping<br />

into one another in watery swirls would be unlikely to<br />

form the complex molecules characteristic <strong>of</strong> life. In many<br />

chemical reactions, solid surfaces allow the orderly catalysis<br />

<strong>of</strong> reactions. The catalytic converter <strong>of</strong> an automobile<br />

uses surfaces <strong>of</strong> the metal palladium to catalyze the reaction<br />

that eliminates carbon monoxide from auto exhaust.<br />

J. D. Bernal, a British biochemist, first proposed the possibility<br />

that the synthesis <strong>of</strong> large molecules from small ones<br />

may have occurred on clay mineral surfaces. Clays certainly<br />

provide an enormous amount <strong>of</strong> surface area for such reactions<br />

to take place. Leslie Orgel calls this possibility “life<br />

on the rocks” and has demonstrated that RNA molecules<br />

<strong>of</strong> length up to 40 bases can be produced on a mineral surface.<br />

RNA molecules <strong>of</strong> this size would be long enough to<br />

get the RNA world (see below) started.<br />

B. Assembly <strong>of</strong> complex chemical systems. Modern life,<br />

even <strong>of</strong> the simplest bacteria, is too complex to have arisen<br />

directly. In particular, the elegant genetic system <strong>of</strong> DNA (see<br />

DNA [raw material <strong>of</strong> evolution]) must represent an<br />

advanced system not found in the first life-forms. In modern<br />

cells, DNA stores genetic information, which is transcribed<br />

into RNA, which directs the formation <strong>of</strong> proteins. As microbiologist<br />

Carl Woese proposed in 1967 (see Woese, Carl<br />

R.), scientists realize that a simpler genetic system <strong>of</strong> life must<br />

have preceded that <strong>of</strong> DNA in the modern cell. Once modern<br />

DNA cells came into existence, they would have outcompeted<br />

the more primitive form which, therefore, no longer exists.<br />

Suggestions (not all mutually exclusive) include:<br />

• Some scientists, such as Stuart Kaufmann, Gunter<br />

Wächtershäuser, and Christian de Duve, have proposed<br />

that metabolic systems (such as glycolysis, which releases<br />

energy from sugar so that organisms can use the energy to<br />

operate) preceded genetic systems. This suggestion has met<br />

with skepticism among most scientists because, at some<br />

point, a genetic system would have to take over the control<br />

<strong>of</strong> the cell.<br />

• The first genetic system may have been formed <strong>of</strong> clay mineral<br />

crystals rather than <strong>of</strong> organic molecules. In this scenario,<br />

proposed by British scientist Graham Cairns-Smith,<br />

organic molecules such as RNA helped the mineral crystals<br />

in their replication. Later, the minerals served as scaffolding<br />

for the reactions <strong>of</strong> the organic molecules, which later<br />

took place without the scaffolding.<br />

• The first genetic molecule may have been something like<br />

TNA (threonucleic acid) or PNA (peptide nucleic acid).<br />

The formation <strong>of</strong> such molecules could have occurred more<br />

readily on the early Earth (in particular, TNA contains no

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