Water is the predominant chemical
component of living organisms. Its unique physical properties, which include
the ability to solvate a wide range of organic and inorganic molecules, derive
from water’s dipolar structure and exceptional capacity for forming hydrogen
bonds. The manner in which water interacts with a solvated biomolecule
influences the structure both of the biomolecule and of water itself. An
excellent nucleophile, water is a reactant or product in many metabolic
reactions. Regulation of water balance depends upon hypothalamic mechanisms
that control thirst, on antidiuretic hormone (ADH), on retention or excretion
of water by the kidneys, and on evaporative loss. Nephrogenic diabetes
insipidus, which involves the inability to concentrate urine or adjust to
subtle changes in extracellular fluid osmolarity, results from the
unresponsiveness of renal tubular osmoreceptors to ADH. Water has a slight
propensity to dissociate into hydroxide ions and protons. The concentration of
protons, or acidity, of aqueous solutions is generally reported using the
logarithmic pH scale. Bicarbonate and other buffers normally maintain the pH of
extracellular fluid between 7.35 and 7.45. Suspected disturbances of acid-base
balance are verified by measuring the pH of arterial blood and the CO2 content
of venous blood. Causes of acidosis (blood pH <7.35) include diabetic
ketosis and lactic acidosis. Alkalosis (pH >7.45) may follow vomiting of
acidic gastric contents.
WATER IS AN IDEAL BIOLOGIC SOLVENT
1.
Water Molecules Form Dipoles
A water molecule is an irregular, slightly skewed
tetrahedron with oxygen at its center. The two hydrogens and the unshared
electrons of the remaining two sp3-hybridized orbitals occupy the corners of
the tetrahedron. The 105° angle between the two hydrogen atoms differs slightly
from the ideal tetrahedral angle, 109.5°. Ammonia is also tetrahedral, with a
107° angle between its three hydrogens. The strongly electronegative oxygen
atom in a water molecule attracts electrons away from the hydrogen nuclei,
leaving them with a partial positive charge, while its two unshared electron
pairs constitute a region of local negative charge. A molecule with electrical
charge distributed asymmetrically about its structure is referred to as a
dipole. Water’s strong dipole is responsible for its high dielectric constant.
As described quantitatively by Coulomb’s law, the strength of interaction F
between oppositely charged particles is inversely proportionate to the
dielectric constant ε of the surrounding medium. The dielectric constant for a
vacuum is essentially unity; for hexane it is 1.9; for ethanol, 24.3; and for water
at 25°C, 78.5. Water therefore greatly decreases the force of attraction
between charged and polar species relative to waterfree environments with lower
dielectric constants. Its strong dipole and high dielectric constant enable
water to dissolve large quantities of charged compounds such as salts.
2.
Water Molecules Form hydrogen Bonds
A partially unshielded hydrogen nucleus covalently
bound to an electron-withdrawing oxygen or nitrogen atom can interact with an
unshared electron pair on another oxygen or nitrogen atom to form a hydrogen
bond. Since water molecules contain both of these features, hydrogen bonding
favors the self-association of water molecules into ordered arrays. Hydrogen
bonding profoundly influences the physical properties of water and accounts for
its relatively high viscosity, surface tension, and boiling point. On average,
each molecule in liquid water associates through hydrogen bonds with 3.5
others. These bonds are both relatively weak and transient, with a half-life of
a few picoseconds. Rupture of a hydrogen bond in liquid water requires only
about 4.5 kcal/ mol, less than 5% of the energy required to rupture a covalent
O—H bond.
Hydrogen bonding enables water to dissolve many organic
biomolecules that contain functional groups which can participate in hydrogen
bonding. The oxygen atoms of aldehydes, ketones, and amides, for example,
provide lone pairs of electrons that can serve as hydrogen acceptors. Alcohols,
carboxylic acids, and amines can serve both as hydrogen acceptors and as donors
of unshielded hydrogen atoms for formation of hydrogen bonds.
Daftar Pustaka
Farrier, Dennise .2014.Biokimia Lippincott; Jakarta, Binapura. Ed:6
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