Molec Cell Ch 2 chemical components of cells

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Last updated 6:55 PM on 7/12/26
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55 Terms

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Covalent bond

Formed by unequal sharing of electrons.

  • strong enough to survive conditions inside cell

  • v. strong, creates polar bonds

Covalent bonds in the cell are rapidly broken by enzyme catalysis that is specific between protein and substrate

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Ionic bonds

Formed by the gain and loss of electrons. (Transfer)

  • One atom becomes positively charged, the other negative (ions)

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Hydrogen bonds

noncovalent attraction between a positively charged hydrogen and an electronegative (or negative) atom. Important for many biological molecules.

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4 weak interactions that help bring molecules together in cells:

van der waals attraction

electrostatic attractions

hydrogen bonds

hydrophobic (nonpolar) interactions.

  • all of these r noncovalent

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There are four major families of small organic (carbon compound) molecules:

1.sugars -> energy sources/subunits of polysacc.

2.fatty acids -> components of cell membranes

3.amino acids -> subunit of proteins

4.nucleotides -> nucleic acids/subunit of RNA/DNA

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What are the large organic molecules created from the small organic building blocks of the cell?

sugars -> polysaccharides and oligosaccharides

fatty acids -> fats and membrane lipids (phospholipids)

amino acids -> proteins

nucleotides -> nucleic acids

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Monosaccharides

Formula of (CH2O)n where n can be 3 (trioses), 4, 5 (pentoses), or 6 (hexoses). Contain either an aldehyde (aldose) or ketone (ketoses) group.

  • monosacc. are subunits used to build carbohydrates

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Monosaccharides

trioses -> pentoses -> hexoses:

Aldoses: glyceraledhyde -> ribose ->glucose

Ketoses : dihydroxyacetone -> ribulose -> fructose

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Disaccharides

The condensation of two monosaccharides produces one disaccharide. -[The carbon that carries the aldehyde/ketone can react with the hydroxyl group on a second sugar molecule to form a disaccharide] -glycosidic bond

Most common:

maltose (glucose + glucose)

lactose (galactose + glucose)

sucrose (glucose + fructose)

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Are glucose, galactose and fructose isomers?

Yes - All have the same formula: C6H12O6

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T or F? Condensation (dehydration) reactions are energetically unfavorable. Hydrolysis reactions are energetically favorable.

True

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T or F? Biological polymers are broken down through hydrolysis reactions.

True

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Fatty acids

All fatty acids have a hydrophilic carboxyl group at one end and a long hydrophobic hydrocarbon tail at the other. The length and extent of saturation vary. Fatty acids with no double bonds in their tail are saturated.

  • essential building blocks for the phospholipids that form the lipid bilayer of cell membranes.

<p>All fatty acids have a<strong> hydrophilic carboxyl group</strong> at one end and a long <strong>hydrophobic hydrocarbon tail</strong> at the other. The length and extent of saturation vary. Fatty acids with no double bonds in their tail are saturated.</p><ul><li><p>essential building blocks for the phospholipids that form the lipid bilayer of cell membranes.</p></li></ul><p></p>
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Triacylglycerols: [three fatty acids]

Fatty acids are stored in cells as an energy reserve (fats and oils) through an ester linkage to glycerol to form triacylglycerols.

  • Connected to glycerol via ester linkages

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Degrees of saturation of fatty acids

-This determines the physical properties of the fat molecules.

  • Saturated fats

    • No double bonds

    • Solid at room temperature

    • Usually made by animals

  • Unsaturated fats

    • Have double bonds

    • Liquid at room temperature

    • Usually made by plants

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Phospholipids (amphipathic) in biological membranes typically contain one saturated and one unsaturated fatty acid. [two fatty acids]

True.

-saturated fatty acids make the membrane less fluid and tend to aggregate.

-cis unsaturated fatty acids reduce membrane rigidity because they do not form solid aggregates.

  • Prevents tight packing

  • Keeps membranes fluid but stable

<p>True.</p><p>-saturated fatty acids make the membrane<strong> less fluid </strong>and tend to aggregate.</p><p>-cis unsaturated fatty acids <strong>reduce membrane rigidit</strong>y because they do not form solid aggregates.</p><ul><li><p>Prevents tight packing</p></li><li><p>Keeps membranes <strong>fluid but stable</strong></p></li></ul><p></p>
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Phospholipid Molecule

hydrophilic head (polar group/phosphate/glycerol) and two hydrophobic fatty acid tails

Phospholipids in cell membranes

  • Typically have:

    • 1 saturated fatty acid

    • 1 cis-unsaturated fatty acid

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Steroids

are another class of lipids and all share a common multiple-ring structure

  • Lipids with a shared core structure

  • Different functions, same backbone

    • ex: testosterone + cholestrol

<p>are <strong>another class of lipids</strong> and all share a common multiple-ring structure </p><ul><li><p>Lipids with a <strong>shared core structure</strong></p></li><li><p>Different functions, same backbone</p><ul><li><p>ex: testosterone + cholestrol</p></li></ul></li></ul><p></p>
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What bonds connect amino acids?

peptide bonds

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R groups/side chains in a.a

the variable chemical groups attached to the alpha-carbon of amino acids that define their unique properties (size, charge, polarity, and hydrophobicity).

There are 20: categorized primarily into nonpolar, polar uncharged, positively charged (basic), and negatively charged (acidic) groups.

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What are the basic (positively charged) side chains?

lysine, arginine, histidine

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What are the acidic (negatively charged) side chains?

aspartic acid, glutamic acid

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What are the uncharged polar side chains?

asparagine, glutamine, serine, threonine, tyrosine

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What are the non polar side chains?

Glycine, Alanine, Valine, Leucine, Isoleucine, Methionine, Cysteine, Phenylalanine, Tryptophan, Proline

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What bond can form between two cysteine side chains?

covalent disulfide bond

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What bond links nucleotides? and how are they produced?

phosphodiester bonds produced by RNA or DNA Polymerase

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What is the structural difference between DNA and RNA?

DNA is double stranded and RNA is single stranded.

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diff btwn DNA and RNA

DNA uses deoxyribose sugar and thymine (T), whereas RNA uses ribose sugar and uracil (U)

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DNA polymerase and RNA polymerase read the template strand in ______ direction.

read the template strand in the 3’ to 5’ direction.

they synthesize the new, complementary polynucleotide chain—whether it is DNA or RNA—in the 5’ to 3’ direction.

  • This ensures the new strand is antiparallel to the template

<p><strong>read </strong>the template strand in the 3’ to 5’ direction. </p><p> they <strong>synthesize </strong>the new, complementary polynucleotide chain—whether it is DNA or RNA—in the 5’ to 3’ direction. </p><ul><li><p>This ensures the new strand is antiparallel to the template</p></li></ul><p></p>
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What percent of the bacterial cell is chemical?

30%

  • other 70% is water

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The 30% chemical of the bacterial cell is made up of what?

inorganic ions (1%)

small molecules (3%)

phospholipids (2%)

DNA (1%)

RNA (6%)

protein (15%)

polysaccharide (2%)

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What are the 4 classes of macromolecules and what are their roles in the cell?

1) polysaccharides (sugars) - energy source/subunit

2) fats/oils (fatty acids) - form cell membranes, steroids,

3) proteins (amino acids) - enzymes

4) nucleic acid (nucleotides)- DNA/RNA, ATP, cyclic AMP, coenzyme A (CoA)

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What are the building blocks of these molecules ?

1) sugars

2) fatty acids

3) amino acids

4) nucleic acid

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How do these macromolecules form?

1) Condensation/ dehydration reaction of two monosaccharides produces one disaccharide with a glycosidic bond.

disaccharides - maltose, lactose, sucrose.

2) Fatty acids are stored as energy reserves (fats/oils) through an ester linkage to glycerol to form triacylglycerols.

3) Peptide bonds connect amino acids to form proteins.

4) Nucleotides are linked by phosphodiester bonds which are produced by DNA or RNA polymerases.

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What are the roles of covalent vs non covalent interactions in the formation of molecules and structures in the cell?

Covalent bonds are strong enough to survive conditions within the cells.

Noncolvalent bonds are how molecules interact with one another.

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glycosidic bonds

Join sugars together

  • Formed by condensation (dehydration) reactions

    • Water is released

  • Two monosaccharides → one disaccharide

energetically UNFAVORABLE

<p>Join sugars together</p><ul><li><p>Formed by <strong>condensation (dehydration) reactions</strong></p><ul><li><p>Water is released</p></li></ul></li><li><p>Two monosaccharides → <strong>one disaccharide</strong></p></li></ul><p>energetically UNFAVORABLE</p>
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condensation/dehydration rxn

  • They require an input of energy, so energetically UNFAVORABLE

  • In cells, enzymes and activated intermediates are used to make this happen

  • Requires energy → ATP (directly or indirectly)

produce water as a byproduct when two molecules combine to form a larger one

<ul><li><p>They <strong>require an input of energy, so energetically UNFAVORABLE</strong></p></li><li><p>In cells, enzymes and activated intermediates are used to make this happen</p></li><li><p>Requires energy → ATP (directly or indirectly)</p></li></ul><p><span><strong><span>produce water </span></strong><span>as a byproduct when two molecules combine to form a larger one</span></span></p>
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hydrolysis rxn

  • Hydrolysis (breaking the bond using water)

  • Energetically favorable

  • Happens easily during digestion and metabolism

  • Does NOT use ATP

  • Releases energy

polymers broken down

<ul><li><p><strong>Hydrolysis</strong> (breaking the bond using water)</p></li><li><p><strong>Energetically favorable</strong></p></li><li><p>Happens easily during digestion and metabolism</p></li></ul><ul><li><p><strong>Does <u>NOT </u>use ATP</strong></p></li><li><p>Releases energy</p></li></ul><p>polymers broken down</p>
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polymer formation + breakdown

  • Condensation reactions

    • Build polymers

    • Require energy (energetically unfavorable)

  • Hydrolysis reactions

    • Break polymers apart

    • Release energy (energetically favorable)

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sat. fatty acids

  • No double bonds

  • Solid at room temperature

  • Usually made by animals

  • STRAIGHT

<p></p><ul><li><p><strong>No </strong>double bonds</p></li><li><p><strong>Solid at room temperature</strong></p></li><li><p>Usually made by animals</p></li><li><p>STRAIGHT</p></li></ul><p></p>
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unsat. fatty acids

  • Have double bonds

  • Liquid at room temperature

  • Usually made by plants

  • KINKED

<p></p><ul><li><p>Have double bonds</p></li><li><p><strong>Liquid at room temperature</strong></p></li><li><p>Usually made by plants</p></li><li><p>KINKED</p></li></ul><p></p>
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ester linkage

a condensation reaction between the carboxyl group of a fatty acid and a hydroxyl group of an alcohol, usually glycerol.
- This linkage is crucial for forming triacylglycerols (fats/oils), phospholipids, and waxes

  • fatty acids r stored as energy reserves through ester linkage to glycerol to form triaglycerols

<p>a condensation reaction between the carboxyl group of a<strong> fatty acid</strong> and a hydroxyl group of an alcohol, usually <strong>glycerol</strong>. <br>  - This linkage is crucial for forming triacylglycerols (fats/oils), phospholipids, and waxes</p><ul><li><p>fatty acids r stored as energy reserves through ester linkage to glycerol to form triaglycerols</p></li></ul><p></p>
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peptide bond

Link amino acids together

  • Formed by dehydration reactions

  • Catalyzed by the ribosome peptidyl transferase

  • Protein has that connect:

    • Amino (N) terminus

    • Carboxyl (C) terminus

N-C-C N-C-C

<p>Link amino acids together</p><ul><li><p>Formed by <strong>dehydration reactions</strong></p></li><li><p>Catalyzed by the <strong>ribosome peptidyl transferase</strong></p></li><li><p>Protein has that connect:</p><ul><li><p><strong>Amino (N) terminus</strong></p></li><li><p><strong>Carboxyl (C) terminus</strong></p></li></ul></li></ul><p>N-C-C  N-C-C</p>
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nucleotides

the subunits of DNA and RNA.

made up of Sugar + base + 1–3 phosphate groups

  • Nucleotides linked by phosphodiester bonds

  • Bond forms between:

    • 5′ phosphate of incoming nucleotide

    • 3′ hydroxyl of previous nucleotide

  • Catalyzed by DNA or RNA polymerase

  • Usually use triphosphate nucleotides

Other Roles :

  • Store energy (ATP)

  • Cell signaling (cAMP)

  • Parts of coenzymes (CoA or coenzyme A)

<p>the subunits of DNA and RNA.</p><p>made up of Sugar + base + <strong>1–3 phosphate groups</strong></p><ul><li><p>Nucleotides linked by <strong>phosphodiester bonds</strong></p></li><li><p>Bond forms between:</p><ul><li><p>5′ phosphate of incoming nucleotide</p></li><li><p>3′ hydroxyl of previous nucleotide</p></li></ul></li><li><p>Catalyzed by <strong>DNA or RNA polymerase</strong></p></li><li><p>Usually use <strong>triphosphate nucleotides</strong></p></li></ul><p><u>Other Roles :</u></p><ul><li><p>Store energy (ATP)</p></li><li><p>Cell signaling (cAMP)</p></li><li><p>Parts of coenzymes (CoA or coenzyme A)</p></li></ul><p></p>
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purines

  • adenine

  • guanine

have 2 nitrogen rings

A=T
G=-C

A=U

<ul><li><p>adenine</p></li><li><p>guanine</p></li></ul><p>have 2 nitrogen rings</p><p>A=T<br>G=-C</p><p>A=U</p>
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pyrimidines

  • uracil

  • cytosine

  • thymine

one nitrogen ring

<ul><li><p>uracil</p></li><li><p>cytosine</p></li><li><p>thymine</p></li></ul><p>one nitrogen ring</p><p></p>
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phosphodiester bond

links nucleotides to create DNA and RNA

  • produced by DNA or RNA polymerases

  • links 5’P of incoming nucleotide w/ 3’ OH of previous nucleotide

Usually use triphosphate nucleotides used during polymerization

<p>links nucleotides to create DNA and RNA</p><ul><li><p>produced by DNA or RNA polymerases</p></li><li><p>links 5’P of incoming nucleotide w/ 3’ OH of previous nucleotide</p></li></ul><p>Usually use <strong>triphosphate nucleotides used during polymerization</strong></p>
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nucleotide base pair bonding

A=T

A=U

G=-C

<p>A=T</p><p>A=U</p><p>G=-C</p>
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amino acids

Small organic molecule containing both an amino group (-NH2) and a carboxyl group (-COOH)

  • it serves as the building block of proteins.

  • All amino acids have an amino group, a carboxyl group, and a side chain (R) attached to their α-carbon atom.

  • amino acids joined together by peptide bonds to build proteins

<p>Small organic molecule containing both an amino group (-NH2) and a carboxyl group (-COOH)</p><ul><li><p> it serves as the building block of proteins.</p></li><li><p>All amino acids have an amino group, a carboxyl group, and a side chain (R) attached to their α-carbon atom.</p></li><li><p>amino acids joined together by peptide bonds to build proteins</p></li></ul><p></p>
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nucleic acid chain synthesis

synthesized from energy-rich nucleoside triphosphates by a condensation reaction that releases pyrophosphate—a pair of phosphate groups linked by a single phosphoanhydride bond

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noncovalent bonding w/ macromolecules

Noncovalent Bonds Also Allow a Macromolecule to Bind Other Selected Molecules

  • Noncovalent Bonds Specify the Precise Shape of a Macromolecule

  • Enzymes recognize their substrates via noncovalent bonds

  • can also stabilize associations between any two macromolecules

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What are the 4 classes of macromolecules and their roles in the cell?

  • Carbohydrates: Provide energy, store energy, and help with cell recognition and structure.

  • Lipids: Form cell membranes, store long-term energy, and act in signaling.

  • Proteins: Carry out most cell functions (enzymes, structure, transport, signaling).

  • Nucleic acids: Store and transmit genetic information (DNA and RNA).

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How do these macromolecules form?

  • They form through dehydration (condensation) reactions, which remove water to create covalent bonds.

  • They are broken down by hydrolysis, which adds water.

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Does the synthesis of macromolecules require or release energy?

  • Requires energy (endergonic process), often using ATP or activated molecules.

  • - condensation rxn

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What are the roles of covalent vs noncovalent interactions in the cell?

  • Covalent bonds hold macromolecules together (e.g., peptide bonds, glycosidic bonds).

  • Noncovalent interactions (hydrogen bonds, ionic bonds, hydrophobic interactions) stabilize 3D structures and allow flexibility and regulation.