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Kuliah 2-Biomolekul
Kuliah 2-Biomolekul
Ikatan PEPTIDA
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Nukleus Golgi
MOLEKUL SEL HIDUP
Nukleus JASAD HIDUP
Mitokondria
Badan Golgi
ORGAN
Kloroplas
Ribosom Ikatan non Mitokondria
SEL Kloroplas
Membran Kovalen
Kromatin SISTEM
ORGANEL MULTIENZIM
Unit pembangun
SUPRAMOLEKUL
polisakarida
Asam nukkeat Protein lipida Ikatan MAKROMOLEKULER
kovalen
Mono Asam Mono Asam lemak SATUAN PENYUSUN
nukleatida amino sakarida gliserol
Dinding sel
SENYAWA ANTARA
Tanaman
Bakteri Energi radiasi
fotosintetik
SENYAWA DASAR
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CO2, H2O, N2, PO4-3
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FINGSI PENYUSUN MAKROMOLEKUL
Macromolecule Building Blocks Functions
Cell structure
Enzymes
Proteins Amino acids (20 types) Molecular motors (muscle, etc)
Membrane pumps & channels
Hormones & receptors
Immune system: antibodies
4 Bases: A, C, G, T
Nucleic Acids: DNA
Deoxyribose sugar Storage of hereditary information
(forms a double helix)
Phosphate (genetic code)
Subunits called nucleotides
Nucleic Acids (RNA)
Protein synthesis:
3 types: 4 Bases: A, C, G, U
m-RNA: working copy of genetic
m-RNA Ribose sugar
code for a gene (transcription)
t-RNA Phosphate
t-RNA & r-RNA: translation of the
r-RNA Subunits called nucleotides 7
code
(usually a single strand)
I. Cells Contain Organic Molecules
A. Most Common Elements
1. Most common elements in living things are carbon, hydrogen, nitrogen,
and oxygen.
2. These four elements constitute about 95% of your body weight.
3. Chemistry of carbon allows the formation of an enormous variety of
organic molecules.
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B. Small Molecules Have
Functional Groups
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4. Isomers are molecules with identical molecular formulas
but differ in arrangement of their atoms
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C. Large Organic Molecules Have Monomers
1. Each small organic molecule can be a unit of a large organic molecule called a
macromolecule.
2. Small organic molecules (e.g., monosaccharides, glycerol and fatty acid,
amino acids, and nucleotides) that can serve as monomers, the subunits of
polymers.
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D. Condensation Is the Reverse of Hydration
1. Macromolecules build by different bonding of different
monomers; mechanism of joining and breaking these bonds is
condensation and hydrolysis.
2. Cellular enzymes carry out condensation and hydrolysis of
polymers.
3. Condensation involves a dehydration synthesis because a water is
removed (dehydration) and a bond is made (synthesis).
a. When two monomers join, a hydroxyl (OH) group is
Removed from one monomer and a hydrogen is removed from the
other.
b. This produces the water given off during a condensation reaction.
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4. Hydrolysis (hydration) reactions break down polymers in reverse
of condensation; a hydroxyl (OH) group from water attaches to one
monomer and hydrogen (H) attaches to the other.
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BIOMOLEKUL BERBGAI ORGANEL
NO ORGANEL BIOMOLEKUL
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3 Letter
Amino Acid Codons
Abbreviation
Alanine Ala GCA GCC GCG GCU
Arginine Arg AGA AGG CGA CGC CGG CGU
Aspartic Acid Asp GAC GAU
Asparagine Asn AAC AAU
Cysteine Cys UGC UGU
Glutamic Acid Glu GAA GAG
Glutamine Gln CAA CAG
Glycine Gly GGA GGC GGG GGU
Histidine His CAC CAU
Isoleucine Ile AUA AUC AUU
Leucine Leu UUA UUG CUA CUC CUG CUU
Lysine Lys AAA AAG
Methionine Met AUG
Phenylalanine Phe UUC UUU
Proline Pro CCA CCC CCG CCU
Serine Ser AGC AGU UCA UCC UCG UCU
Threonine Thr ACA ACC ACG ACU
Tryptophan Trp UGG
Tyrosine Tyr UAC UAU
Valine Val GUA GUC GUG GUU
Start AUG 18
Stop UAA UAG UGA
alpha helix
beta strands
turn
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Amino Acids
Name Abbr. Linear structure
formula======================================================
Alanine ala a CH3-CH(NH2)-COOH
Arginine arg r HN=C(NH2)-NH-(CH2)3-CH(NH2)-COOH
Asparagine asn n H2N-CO-CH2-CH(NH2)-COOH
Aspartic acid asp d HOOC-CH2-CH(NH2)-COOH
Cysteine cys c HS-CH2-CH(NH2)-COOH
Glutamine gln q H2N-CO-(CH2)2-CH(NH2)-COOH
Glutamic acid glu e HOOC-(CH2)2-CH(NH2)-COOH
Glycine gly g NH2-CH2-COOH
Histidine his h NH-CH=N-CH=C-CH2-CH(NH2)-COOH
Isoleucine ile i CH3-CH2-CH(CH3)-CH(NH2)-COOH
Leucine leu l (CH3)2-CH-CH2-CH(NH2)-COOH
Lysine lys k H2N-(CH2)4-CH(NH2)-COOH
Methionine met m CH3-S-(CH2)2-CH(NH2)-COOH
Phenylalanine phe f Ph-CH2-CH(NH2)-COOH
Proline pro p NH-(CH2)3-CH-COOH
Serine ser s HO-CH2-CH(NH2)-COOH
Threonine thr t CH3-CH(OH)-CH(NH2)-COOH
Tryptophan trp w Ph-NH-CH=C-CH2-CH(NH2)-COOH
Tyrosine tyr y HO-p-Ph-CH2-CH(NH2)-COOH
Valine val v (CH3)2-CH-CH(NH2)-COOH
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Carbohydrates
Sugar
Sweetness
fructose 173%
sucrose 100%
glucose 74%
maltose 33%
galactose 33%
lactose 16%
Best known sugars have six
Disaccharides carbons (hexoses)
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. Polysaccharides are chains of glucose
molecules or modified glucose molecules
. Starch is straight chain of glucose Glycogen is highly branched polymer of glucose with
many side branches; called "animal starch," it is
molecules with few side branches storage carbohydrate in the liver of animals.
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Starch Molecules
(14) linkage
amylose (20-30%)
Mol. Wt.~104-106 g/mol
amylopectin (70-80%)
(14) linkage
Branching does not allow for as much inter-molecular interaction; easy to overcome
structure; starch is hydrated.
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amylose: (14)
frustrated packing and less H-bonding: coils and in case of amylopectin forms helix
cellulose: (14)
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Nucleotides
a. Nucleotides of DNA contain deoxyribose
sugar; nucleotides of RNA contain ribose.
NAD+, adalah koenzim yang ditemukan di semua sel hidup. Senyawa ini berupa
dinukleotida, yakni mengandung dua nukleotida yang dihubungkan melalui
gugus fosfat, dengan satu nukleotida mengandung basa adenina dan yang lainnya
mengandung nikotinamida.
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FADH
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