Nitrogen Flashcards

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1
Q

Nitrogen fixing requires

A

nitrogenase

lots of energy

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2
Q

nitrogenase is inactivated by

A

oxygen

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3
Q

Leguminous plants produce leghemoglobin which binds O2 allowing the concentration to be…

A

low enough to allow nitrogenase to work

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4
Q

nitrogen fixation produces

A

ammonia

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5
Q

once ammonia is fixed it is converted into ……..

a usable form of nitrogen taken up by plants and microbes

A

nitrate

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6
Q

Flow of nitrogen from ammonia to other biomolecules occurs through

A

glutamate

eg Urea

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7
Q

Transamination

A

transferring amino groups between different molecules

in order to conserve nitrogen

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8
Q

a chemical reaction that transfers an amino group to a ketoacid to form new amino acids.

A

transamination

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9
Q

aminotransferases

A

intracellular enzymes

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10
Q

glutamate can only ‘lose’ nitrogen by

A

transamination

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11
Q

Humans excrete nitrogen as

A

urea and uric acid

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12
Q

Ammonia is transported in the bloodstream safely as

A

glutamate

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13
Q

Glutamate can donate ammonia to ………. to make …………

A

pyruvate

alanine

(or can be made into glutamine)

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14
Q

Glycolysis yields

A

pyruvate

if not eliminated LACTIC ACID will build up

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15
Q

excess pyruvate can be converted to………. for transport to the

A

alanine

liver

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16
Q

what charge does glutamate have?

A

negative

-ve

17
Q

what charge do alanine and glutamine have?

A

no charge

18
Q

charged molecules don’t pass through membranes so easy - they have to be converted to

A

uncharged molecules

19
Q

Catabolism of amino acids involves transfer of the amino group via PLP-dependent aminotransferase to a donor such as………. to yield

A

alpha-ketoglutarate

glutamine

20
Q

toxic ammonia is quickly recaptured into carbamoyl phosphate and passed into

A

the urea cycle

21
Q

L-glutamine can be used to create new …………. or it can dispose of……..

A

amino acids

excess nitrogen via ammonia

22
Q

Most inherited metabolic disorders are

A

autosomal recessive inheritance

23
Q

there are ….. inherited disorders of the urea cycle

A

6

24
Q

urea cycle defects are most common in ………………… deficiency

A

ornithine transcarbamoylase (OTC)

25
Q

OTC has …………. inheritance

A

x - linked

26
Q

Phenylketonuria

A

absence of phenylalanine hydroxylase (PAH)

increased phenylalanine levels

27
Q

Phenylketonuria treatment

A

low protein diet supplemented with protein substitute