Module 1: Foundations Flashcards

(24 cards)

1
Q

what are the 4 most abundant elements in the body

A

carbon, oxygen, hydrogen, nitrogen

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2
Q

what is the base of all know life forms

A

carbon

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3
Q

where do we obtain carbon

A

from air through plants

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4
Q

where do obtain oxygen

A

air

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5
Q

where do we obtain hydrogen

A

from water

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6
Q

where do obtain nitrogen

A

from plants which extract it from the spoil
needs to be in more reactive nitrate form

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7
Q

why is life carbon based

A

extremely versatile in terms of bonding capacity- single, double, triple
enables creation of complex molecules

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8
Q

what is the second best candidate for chemical foundation of life

A

silicon
very similar to carbon as it can form 4 covalent bonds

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9
Q

why is life carbon based and not silicon based

A

carbon- carbon bonds are stronger
more energy is released on combustion of carbon-carbon bonds
combustion product of carbon is carbon dioxide and remain in biosphere but silicon combustion product is pretty much sand

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10
Q

what bonds hold proteins together

A

non covalent bonds
making them easier to fold and less stable

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11
Q

why are weak bonds in proteins good

A

gives them the ability to be versatile
weak and transient bonds are needed and serve as a advantage

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12
Q

what are the disadvantages of weak bonds in proteins

A

slightly heating, change in pH, and pressure can causes misfolding and unfolding of proteins

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13
Q

what is the structure function relationship

A

the structure of biomolecules dictate their function

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14
Q

conformation

A

flexible spatial arrangement of atoms within a molecule
changes in 3D shapes, like different folding patterns

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15
Q

configuration

A

fixed spatial arrangement of atoms within a molecule
cannot be changed without breaking a covalent bond
double bonds or chiral carbons
cis and trans isomer structures

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16
Q

geometric isomers

A

the same chemical formula but differ in the configuration of groups in respect to non rotating double bond

17
Q

cis configuration

A

groups on the same side of the double bond

18
Q

trans configuration

A

groups on opposite side of double bonds

19
Q

chiral carbons

A

4 different substituent groups attached these groups may be arranged in different ways in space yielding two stereoisomers that differ in their configuration

20
Q

are the chemical and biological properties similar in stereoisomers

A

chemical properties are similar and biological activities are often distinct

21
Q

rules of chiral carbons

A

no double or triple bonds, cant have identical groups, alpha carbon is the middle one

22
Q

construction

A

biomolecules usually constructed from exclusively one stereoisomer proteins are built from L-amino acids

23
Q

interactions

A

interactions between biomolecules as well as between biomolecules and small molecules are stereospecific