Lecture 10 Part 2 Flashcards

1
Q

what occurs when there is an AA deficiency

A
  • poor growth
  • reduced milk and egg production
  • anorexia
  • infertility
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2
Q

absorption of proteins and AAs during 1st 24 hours after birth

A
  • large proteins
  • immunoglobins from colostrum
  • these large particles wont be able to be digested after first 24 hours
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3
Q

absorption after 24 hours

A

proteins digested and absorbed as AAs and peptides

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4
Q

digestion of proteins

A
  • begins in gastric stomach
  • small intestine (pancreatic region) that gives products of free AA, dipeptides, and tripeptides
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5
Q

pepsinogen + HCL=

A

pepsin

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6
Q

what hydrolyzes peptide bonds between specific AAs

A

Pro carboxypeptidase–> carboxypeptidase

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7
Q

absorption of AAs and peptides

A
  • occurs in small intestine
  • free AAs absorbed by active transport systems
  • absorption rate vary
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8
Q

ruminant absorption of AAs and peptides

A

may also occur in rumen and omasum

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9
Q

where are dipeptides and tripeptides absorbed

A
  • into mucosal cells
  • hydrolyzed to FAA before entering circulation
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10
Q

what are AAs used for

A
  • tissue protein synthesis
  • synthesis of enzymes, hormones, other metabolites
  • transamination-AA biosynthesis
  • deamination and use of carbon skeleton for energy
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11
Q

tissue protein synthesis

A
  • occurs in every cell of body, hormonal control
  • takes place at ribosome
  • requires tRNA, rRNA, mRNA, DNA
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12
Q

tRNA

A

caries specific AA and base pairs with mRNA

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13
Q

rRNA

A

part of ribosome

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14
Q

mRNA

A

determines AA sequence of a protein
- codons of 3 nucleotides

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15
Q

DNA

A

genetic code

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16
Q

tissue protein degradation

A
  • breakdown of proteins
  • fate of AAs from protein degradation
17
Q

breakdown of proteins

A
  • requires proteases
  • breakdown to AAs
  • stimulated by glucocorticoids
18
Q

what are the fate of AAs from protein degradation

A
  • used in synthesis of protein
  • broken down to NH2 and carbon skeleton if body needs energy
19
Q

what are the 2 processes in AA breakdown

A
  • deamination
  • transamination
20
Q

deamination

A
  • NH2 removed—> ammonia
  • ammonia disposed thru urea cycle
  • C skeleton–> keto acid, or gluconeogenesis, or ketogenesis
21
Q

transamination

A
  • resynthesis of AA
  • transfer NH2 from AA–>keto acid—>NEAA
  • C skeleton—>keto acid, or gluconeogenesis, or ketogenesis
22
Q

what are strictly ketogenic

A

leucine and lysine

23
Q

why do some AAs have different fats

A

due to structural uniqueness

24
Q

urea cycle

A
  • excretion of excess N
  • occurs in kidney and liver
  • several complex steps
  • energy expending
25
what are the different forms of N for different animals
fish= ammonia birds, snakes, lizards= uric acid terrestrial vertebrates and sharks= urea
26
how is urea excreted and recyclized
- excreted in urine - in ruminants, recycled thru salvia to help fuel microbes
27
LAAs
limiting amino acids
28
what are the pre ruminants similar too when it comes to AA requirements
nonruminants
29
MCP
ruminally synthesized microbial protein
30
what are unprotected AAs
degraded
31
how do proteins vary
in degree of degradation - RDP or DIP - RUP or UIP
32
RDP and DIP
ruminally degraded protein degraded intake protein - same thing/meaning
33
RUP or UIP
ruminally degraded protein undegraded intake protein - same thing/meaning - bypass protein
34
how does protein degradation and AA and protein synthesis happen
by rumen microbes
35
bacterial proteins
- high quality - quantity limits