part 3- bio chem Flashcards

1
Q

R=H

A

glycine

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2
Q

R=CH3

A

alanine

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3
Q

R=CH2CH(CH3)2

A

leucine

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4
Q

R=CH2OH

A

serine

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5
Q

R=CH2SH

A

cysteine

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6
Q

R=CH2COOH

A

aspartic acid

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7
Q

R=(CH2)4NH2

A

lysine

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8
Q

zwitterion

A

amino acid is in water it will ionize
NH2 will be NH3+
COOH will be COO-

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9
Q

amino acid has

A

carboxylic acid, one amine, one H, and one R

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10
Q

what is formed when two amino acid molecules are linked by a reaction that results in the loss of a water molecule

A

a peptide

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11
Q

A Peptide bond is an example of a

A

amide

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12
Q

the shape of a peptide bond is

A

flat due to the partial double bonds joining C, O, and N

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13
Q

enzyme that breaks up fat is

A

lipases

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14
Q

primary

A

primary- sequence of amino acid

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15
Q

secondary

A

secondary- primary structure twisted into an a-helix, b- pleated sheet or triple helix held together by hydrogen bond between the peptide bonds along the chain

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16
Q

tertiary

A

tertiary- secondary structure folds into a compact, 3-D shape stabilized by interaction g between R groups (hydrophobic and hydrophilic interaction, salt bridges, hydrogen bonds, disulfide bonds)

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17
Q

quaternary

A

two or more protein subunits combined to form a biologically active protein

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18
Q

which of the following classes of compounds provide both an energy source and structural material when metabolized

A

proteins

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19
Q

denature

A

heat, acid, base, alcohol, heavy metals, and agitation

20
Q

which vitamin is fat soluble

A

D

21
Q

which vitamin is responsible for blood clotting

A

K

22
Q

monosaccharides

A

end in ose
3-6 carbon atoms, carbonyl group (aldehyde or ketone) and several hydroxyl groups

glucose and fructose

23
Q

aldoses

A

are monosaccharides with the aldehyde functional group
aldohexose- C6
aldopentose- C5

24
Q

ketose

A

monosaccharides with ketone functional group

ketohexose- C6

25
Q

mutarotation

A

interconversion between a and b isomers

26
Q

epimers

A

monosaccharides that show inversion of configuration at a single chiral carbon

27
Q

what is the name of the mechanisms that converts D-glucose into D-mannose

A

epimerization

28
Q

glycosidic bond

A

joining monosacharides

forms disaccharide and water

29
Q

simple lipids

A

steroids and terpenes

the are not the result of condensation reaction and are not made of from fatty acid

30
Q

complex lipids

A

triglycerides and phospholipids
condensation of fatty acids and alcohol to form ester

saturated and unsaturated

31
Q

waxes

A

ester

32
Q

triglycerides

A

three esters

33
Q

phospholipids

A

two esters and two phosphoesters

34
Q

ester functional group result from

A

condensation of carboxylic acid and alcohol

35
Q

acid hydrolysis of triglyceride

basic hydrolysis of triglyceride

A

acid- glycerol and fatty acid

basic- hydrolysis and salt of fatty acids (soap)

36
Q

micelle

A

encapsulate grease with their nonpolar ends and face the outside water environment with their polar ends.
soap molecules

the structure is called micelle

37
Q

storage of triglyceride

A

triglycerides with saturated fatty acidy, solid at room temperature
triglycerides with unsaturated, oil at room temperature
stored in our adipose tissue

38
Q

Glycerol reaction with a fatty acid yields?

A

lipid

39
Q

a lipid triglyceride is formed by a reaction of

A

fatty acid and glycerol

40
Q

fatty acids are stored in adipose tissue as

A

triglycerides

41
Q

a micelle is likely formed from

A

fatty acids

42
Q

Steroids

A
  • compounds containing the steroid nucleus which is 3 cyclohexane and 1 cyclopentane
  • Cholesterol is the most abundant steroid in the body
  • Steroid hormones are derivatives of cholesterol (sex hormones, testosterone, estrogen, and progesterone)
43
Q

Terpenes

A
  • made of repeating isoprene unite (2-methyl, 1-3-butene)
  • steroids are derivatives of the triterpene squalene
    example= vitamin A
44
Q

How to develop nucleic acid?

A

condensation/hydrolysis

1) sugar and base is condensed to form a nucleoside (key bond formed is N-glycosidic bond)
sugar+base=nucleoside + water
2) nucleoside and phosphate group condense and form a nucleotide (key bond formed is phosphoester)
nucleoside+ phosphate= nucleotide + water
3) condense 3-OH- group of the sugar in one nucleotide to the phosphate group on the 5’carbon atom of the next nucleotide
nucleotide+nucleotide= dinucleotide+ water

45
Q

double helix formed

A

A-T- two hydorgens

G-C three hydrogens

46
Q

mRNA

A

3 base codon