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The Central Dogma
A theory that states information in an organism that decides an organism, and describes everything that it can do, is encoded in the DNA
DNA is then copied into RNA, which is very similar, it has exactly the same sequences as DNA, but can easily be changed
From the information in the RNA, you can make protein by reading the sequences of bases in the RNA 3 at a time & 3 code for one amino acid
The Central Dogma (cont.)
Information from nucleic acids cannot be back-engineered
Nucleic acids → protein
Protein Synthesis: Transcription & Translation
In the nucleus the blueprint or code, for the protein is copied or transcribed from the DNA gene into a molecule of messenger RNA
The mRNA takes the genetic information from the nucleus to structures called ribosomes in the cytosol, where proteins are made
In the cytosol, transfer RNA reads the genetic code & delivers the needed amino acids to the ribosome to form a polypeptide chain
Amin Acid Pool Allows for Amino Acid Availability
Amino Acid Pool
an accumulation of amino acids in the liver & blood that adjusts to meet the body’s need for protein & amino acids
Limiting amino acid
Our bodies use amino acids in a specific ratio to each other, so if a person doesn’t get enough of one of them to match w/ the rest, the rest can only be used at a level to balance w/ that low one
The amino acid that is deficient in the diet is the limiting amino
Metabolism, Physiology, Behavior
Metabolism ←> Physiology ←> Behavior
Pathways of amino acid metabolism
Amino Acids: Transamination
When a nonessential amino acid is not available from the diet, it can be made in the body by the process of transamination
Deamination & Synthesis of a Nonessential Amino Acid
The deamination of an amino acid produces ammonia & a keto acid (removal of an amino group)
Given a source of ammonia, the body can make nonessential amino acids from keto acids
Energy Production from Protein
The amino group is removed by deamination
Deamination of some amino acids produces 3-carbon molecules that can be used to synthesize glucose, via gluconeogenesis
Deamination of some amino acids results in 2-carbon molecules that form acetyl-CoA, which can enter the citric acid cycle or be used to synthesize fatty acids
Deamination of some amino acids forms molecules that are intermediates in the citric acid cycle
High-energy electrons from the breakdown of amino acids are transferred to the electron transport chain where the energy is trapped & used to produce ATP & water
Urea Synthesis
Amino acids are deaminated before they can be metabolized to produce ATP or used to synthesize glucose or fat
The amino group forms toxic ammonia
Ammonia is converted into urea in the liver
Urea can safely travel in the blood & is filtered out of the blood by the kidney & eliminated from the body in the urine
Nitrogen Balance
B = I - (U + F +S)
B is nitrogen balance
I is nitrogen intake
U is urinary nitrogen
F is fecal nitrogen
S loss of nitrogen through the skin
Proteins in the Diet
Recommended protein intake:
Adult RDA = .8g/kilogram body weight
Infant RDA = 1.5 g/kilogram body weight
Elderly = 1 to 1.2 g/kg
Positive Nitrogen Balance
Situations when positive nitrogen balance occur:
growth
pregnancy
recovery stage after illness/injury
athletic training resulting in increased lean body mass
increase secretion of certain hormones such as insulin, growth hormone, & testosterone
Nitrogen Equilibrium
Situations when nitrogen equilibrium occurs:
healthy adult meeting protein & energy needs
Negative Nitrogen Balance
Situations when negative nitrogen balance occur:
inadequate intake of protein
inadequate energy intake
severe conditions such as fevers, burns, & infections
severe bad rest (for several days)
deficiency of essential amino acids
increased secretion of certain hormones such as thyroid hormone & cortisol
Examples of Protein (Nitrogen) Balance
a pregnant women adds protein so she has a positive nitrogen balance
a healthy person who is neither gaining nor losing nitrogen is in nitrogen equilibrium
a person who is severely ill & losing protein has a negative nitrogen balance
Nitrogen Approximation
Nitrogen makes up approximately 16% of the weight of an amino acid
Nitrogen intake multiplied by 6.25 provides an estimate of protein intake
A crude estimate of the % protein content of food = N x 100/6 = N x 6.25
Apparent digestibility
[N (eaten) - N (fecal) ] / N (eaten) x 100
Protein Efficiency Ratio
PER = live weight gain/crude protein intake
if a particular diet doesn’t support growth, then a PER of 0 will be recorded
Factors that affect protein quality:
digestibility
amino acid content
toxins (trypsin inhibitor)
form of amino acids
When measuring quality of a protein need to consider calorie intake:
Isocaloric diets - Test diet & control diets have the same caloric density
Pair feeding - The caloric intake between subjects on the control & those subjects on the test diet are equal
Protein Complementation
Combining plant protein sources to achieve a better amino acid balance than each would have along
Legumes: peas, beans, lentils, peanuts, alfalfa
Grain: wheat, rice, corn, oats, rye
Proteins that may harm certain individuals: Phenylketonuria
PKU is an inherited condition attributed to a defective gene
Aspartame, a sugar substitute, contains phenylalanine
Protein Deficiency
Protein-energy malnutrition (PEM) is used to refer to the continuum of protein deficiency conditions, ranging from mostly protein deficiency called
1) kwashiorkor
2) marasmus
Kwashiorkor
Severe protein deficit, often accompanied by infections or other diseases
Characteristics:
Edema (swelling)
Mild to moderate weight loss
Maintenance of some muscle & subcutaneous fat
Growth impairment
Rapid onset
Fatty liver
Marasmus
Severe energy & protein deficit
Characteristics:
Severe weight loss
Wasting of muscle & body fat (skin & bones appearance)
Severe growth impairment
Develops gradually
Pros & Cons of Vegetarian Eating
Types of vegetarian diets
semi-vegetarian
lacto-ovo vegetarian
vegan
Health benefits vs. health risks
less fat, saturated fat, & cholesterol
restrictive diets may lack nutrients
careful planning needed for children, pregnant women
Nutrients Supplied by Plant & Animal Foods
Animal products provide sources of:
Protein
B vitamins
Minerals such as iron, zinc, & calcium
However, animal products are low in fiber & can be high in fat
Plant sources of protein are also a good source of:
B vitamins
Iron
Zinc
Fiver
Calcium
But in less absorbable forms
Protein Quality of Various Food Proteins
Food Protein Allergies
Food proteins (allergens) cause an immune response, creating an allergic reaction
IgE most commonly produced (antibodies produced by the immune system)
anaphylaxis (a severe, life-threatening allergic reaction that can occur rapidly after exposure to an allergen)
8 foods account for 90% of all food allergies
peanuts, tree nuts, milk, eggs, fish, shellfish, soy, & wheat
Too Much Protein
heart disease
obesity
cancer
osteoporosis (a bone disease that weakens bones, making them more likely to break)
protein & amino acid supplements
generally not needed w/ risks unknown
kidney stones
hydration & kidney function
Protein Excess
Hydration & kidney function
When protein intake increases above the amount needed, so does the production of protein breakdown products such as urea, which must be eliminated from the body by the kidneys. To do this, more water must be excreted in the urine, increasing water losses
Kidney Stones
The increase in urinary calcium excretion associated w/ high-protein diets has led to speculation that a high protein intake may increase the risk of kidney stones
Heart Disease & Cancer
High-protein diets is related more to the dietary components that accompany animal versus plant proteins. Typically, high protein diets are also high in animal products, this dietary pattern is high in saturated fat & cholesterol & low in fiber
Celiac Disease
wheat or gluten intolerance
found in wheat, rye, & barley
Photosynthesis
Carbohydrates
Macronutrient
4 kcal/g
Carbon, oxygen, hydrogen
Carbon-hydrate: C +H20
CHO
Glucose: C6H1206
Carbohydrates Functions
provides energy
spares protein
provides sweetness
provides fiber
enhances functions of many proteins
Carbohydrate Types
Simple
Monosaccharides (e.g glucose, fructose)
Disaccharides (e.g sucrose “sugar”: glucose + fructose)
Complex (3 or more monosaccharides)
oligosaccharides
polysaccharides (starch, fiber, glycogen)
Monosaccharides
Glucose
most abundant sugar molecule in our diet; good energy source
Fructose
sweetest natural sugar; found in fruit, high-fructose corn syrup
Galactose
does not occur alone in foods; binds w/ glucose to form lactose
Lactose Intolerance
not enough lactase in the SI to digest lactose
symptoms: diarrhea, bloating, intestinal gas
Oligosaccharides
3-10 monosaccharides
Indigestible molecular bonds
Colonic bacteria digest = gas, short chain fatty acids
Insoluble & Soluble Fiber
1) Insoluble fiber
part of cell wall
don’t dissolve in water
contributes bulk to stool
examples: cellulose, hemicellulose
good sources: whole grains, fruits, veggies
2) Soluble Fiber
dissolve in water, are viscous & gel-forming
bacteria metabolize-like oligosaccharides
examples: gums, pectin
good sources: fruits, berries, oats
Polysaccharides
starch: storage form of glucose in plants; food sources include grains, legumes, & tubers
amylose
amylopectin
glycogen: storage form of glucose in animals; stored in liver & muscles
fiber: forms the support structures of leaves, stems, & plants
Fiber: Health Benefits
High fiber diets may:
promote weight loss
promote regular bowel movements
prevent constipation
prevent hemorrhoids & diverticulitis
lower the risk of colon cancer
Soluble Fiber: Health Benefits
lowers cholesterol
soluble fiber binds w/ bile
decreases (re)absorption of bile acids
increases hepatic cholesterol → bile acids
increases LDL uptake by liver
delays rise in blood glucose
fiber in food ‘traps’ nutrients
delays nutrient absorption
stabilizes blood sugar levels
Enterohepatic Circulation of Bile
Whole Grains versus Refined Grains
whole or unrefined grains contain:
bran layers: good source of fiber & vitamins
germ: good source of vegetable oils & vitamin E
endosperm: contains starch & some protein
Fates of Glucose
monosaccharides enter capillaries, travel to liver
in liver cells, fructose & galactose → glucose
Glucose:
used for energy in liver
passed into the blood for other cells to use for energy
store in liver & muscles as glycogen
if consumed in excess energy needs → synthesize fatty acids
Starch breakdown in small intestine
Pancreatic Enzymes
amylase: breaks down carbohydrates (starch) into sugars which are more easily absorbed by the body
also found in saliva
a shortage may cause: diarrhea due to the effects of undigested starch in the colon
Digestion & absorption in the small intestine
Glucose Catabolism: Glycolysis
glyco = sugar, lysis = breakdown
the metabolic pathway that converts glucose into pyruvate
the free energy released in this process is used to form the high-energy compounds ATP
doesn’t require oxygen, it is a way to produce ATP anaerobically (w/o oxygen) and is known as anaerobic cellular respiration
Creating ATP through Cellular Respiration
Glycolysis → citric acid cycle → electron transport chain
Glycogen Levels
Glycogen
storage form of glucose
liver can store 100g glycogen (400 kcal)
used to maintain blood glucose
muscles store 350 g (1400 kcal muscle needs)
Gluconeogenesis
making glucose from non-glucose substrates
glucagon initiates this when CHO intake is low
Overview: Glucose & Glycogen
Exocrine & Endocrine Pancreas and Starch breakdown
Blood Glucose Regulation
insulin: decrease in blood glucose
glucagon: increase blood glucose
Diabetes mellitus (diabetes)
a group of metabolic disorders characterized by a high level of blood sugar over a prolonged period of time
it results from the inability to regulate blood sugar
Blood glucose levels in diabetes
Type 1 Diabetes
Juvenile-onset diabetes
Autoimmune disease affecting beta cells of pancreas
insulin injections
accounts for 5-10% of total diabetes cases in the US
symptoms: frequent urination, unusual thirst, extreme hunger, unusual weight loss, extreme fatigue, irritability, ketone bodies
Type 2 Diabetes
was called adult-onset diabetes or NIDDM
95% of cases in US are T2D
resistance or decrease response to insulin
diet, exercise, oral meds can help control
Types 2 Diabetes Risk Factors
> 45 years old
family history
overweight/obesity (BMI >25)
central weight
sedentary lifestyle
decrease in HDL and/or increase TG
some racial/ethnic groups (Indigenous Americans, African American, Latin American)
Hypoglycemia
low blood sugar (glucose)
causes shakiness, sweating, anxiety
reactive hypoglycemia: pancreas secretes too much insulin after a high-carbohydrate meal
Glycemic Response
a food’s potential to raise blood glucose levels
increase in glycemic index (GI) → increase in blood glucose levels
Influenced by the amount & type of CHO & protein, fat, and fiber content
Glycemic load = GI x CHO grams in food
The Glycemic index
1) High (GI 70+)
2) Medium (GI 55-59)
3) Low (GI 54 or less)
Gluconeogenesis
making glucose from non-glucose substrates
glucagon initiates this when CHO intake is low
Carbohydrates Are Needed to Break Down Fate to carbon dioxide and water
Functions of Lipids (Fat)
provide energy at rest, fasting & during moderate-intensity exercise, prolonged exercise
typical American diet contains about 33%
energy storage (triglyceride in adipose tissue)
padding (protection) & insulation
components of cell membranes
many compounds are synthesized from lipids
absorption & transport fat-soluble vitamins
satiety, flavor, taste, & aroma of foods
Types of Lipid Molecules
Free Fatty Acids
Triglycerides (TG) (Fats)
Phospholipids
Sterols
Fatty acids: Chain length
short chain FA: fewer than 6 carbons butyric acid (butter)
medium chain FA: 6-12 carbons lauric acid (coconut oil)
long chain FA: 14 or more linoleic (safflower oil)
Fatty Acid Structures
saturated fatty acids
unsaturated fatty acids
polyunsaturated
omega-6
omega-3
monounsaturated
Triglycerides
three fatty acid molecules
fatty acids are long chains of carbon atoms bound to each other as well as to hydrogen atoms
one glycerol molecule
glycerol is a 3-carbon alcohol that is the backbone of a triglyceride
Condensation reaction (TG synthesis)
Hydrolysis reaction (lipase)
3 fatty acids + glycerol → triglyceride
are the major form of lipid in the food & in the body
Types of Fatty Acids -Effects on Cholesterol
saturated (SFA): not food
raised cholesterol
coconut oil, palm kernel oil, butter, cream, cheese, beef fat, whole milk
monounsaturated (MUFA): neutral
olive oil, canola oil, peanut oil, cashew nuts
polyunsaturated (PUFA): good
veggie oils, seeds, almonds, walnuts, soy, fish
* shape impacts stacking ability & fluidity
Essential Fatty Acids
are those polyunsaturated fatty acids (PUFA) that must be provided by foods because these cannot be synthesized in the body yet are necessary for health
two families of EFA: omega-3 and omega-6
Essential fatty acid deficiency
are important for growth, skin integrity, fertility, & the structure and function of cell membranes
if adequate amounts of essential fatty acids aren’t consumed, a deficiency can result
symptoms include: dry, scaly skin, live abnormalities, poor wound healing, growth failure in infants, & impaired hearing and vision
Sources of Essential Fatty Acids
omega 6 fatty acids (main dietary source is linoleic)
most vegetable oils, nut & seed oils
omega 3 fatty acids (main dietary source is alpha-linolenic)
soy oil, flaxseed, leafy green vegs
fish have longer chain omega 3: EPA, DHA (can also be produced from dietary alpha-linoleic)
associated w/ reduced heart disease
Omega 6: Omega 3 Requirements
omega 6: omega 3.
10:1
Essential Fatty Acids & Eicosanoid synthesis
the ratio of dietary omega-6 to omega-3 essential fatty acids affects the balance of these fatty acids in the tissues & thus the ratio of the types of eicosanoids made from them
Trans Fatty Acids
can be created during food processing by hydrogenation
hydrogenation causes some double bonds to become saturated
hydrogenated facts can be found in margarines, vegetable shortening & shelf-stable baked goods
trans fatty acids have to be shown to raise blood cholesterol levels & increase the risk of heart disease
Trans Fatty Acids Structure
Phospholipids
2 fatty acids
glycerol
phosphorous -containing molecule
properties: hydrophobic & hydrophilic ends
Function:
helps w/ fat absorption (emulsifier)
lecithin + bile salts + electrolytes = bile
help transport dietary facts in circulation
part of the cell membrane
in food: emulsifier (mayonnaise, salad dressing)
Liver makes phospholipids so not essential
Foods: animal cell membranes, egg yolks
Emulsification
Sterols
4 carbon rings
found in food & made in body
cholesterol is most common dietary sterol -only found in animals
high cholesterol increases CHD risk
plant sterols can reduce CHD risk
Cholesterol (a sterol)
functions:
bile salt precursor
cell membrane structure
hormones (glucocorticoids, estrogen, testosterone)
vitamin D
Sources: produced by animals
animal products
non-essential in the diet
health issue: raises LDL-C cholesterol
General goal <300 mg/day in the diet
3 oz meat ~ 100 mg
Lipid digestion & absorption (a)
Lipids Absorption & Transport
FAs don’t mix well w/ water
bile = emulsifier
micelles formed
transport lipid digestion products into enterocytes
Lipase Action
mouth: not much, some in infants
stomach: gastric lipase… not much
small intestine:
CCK: stimulates gall bladder to release bile & pancreatic lipase
Lipases break TG into monoacylgyceride & 2 free fatty acids
Triglyceride digestion
3 fatty acids bound to glycerol backbone
enzymes in digestive trace (lipases) break down triglyceride and release free fatty acids
Lipid digestion & absorption (b)
Enterohepatic Circulation of Bile
made in the liver, stored in the gall bladder
emulsifies fat, allowing enzymes to hydrolyze it into smaller units that can be absorbed
greenish fluid containing:
bile salts: derived from cholesterol
phospholipids (e.g. lecithin)
cholesterol
bile pigments
bile secretion stimulated by CCK
Lipids in the Body: Absorption & Transport
in the enterocyte:
short & medium chain FA (<14 C chain) enter portal circulation
long chain FA reassembled into TG
combined w/ cholesterol, phospholipids & small protein
you now have a lipoprotein called a chylomicron
chylomicrons enter the lymph then the bloodstream
Lipoprotein
transport lipids & cholesterol in the blood
Lipoproteins: lipids in the blood circulation (transport dietary lipids)
chylomicrons
very low-density lipoproteins (VLDL)
intermediate-density (IDL)
low-density lipoproteins (LDL) - CHD risk
high-density lipoproteins (HDL) - protective
protein components (apolipoproteins) involved in metabolism & final disposition of lipoprotein
Cardiovascular Disease (CVD)
abnormal condition of the heart & blood vessels
atherosclerosis:
narrowing & hardening of blood vessels that supply blood to the heart muscle, brain & other parts of the body
coronary heart disease (CHD)
heart not receiving enough blood
stroke
brain not receiving enough blood
Triglycerides are continuously stored & then broken down, depending on the immediate energy needs of the body
Micronutrients
vitamins & minerals (trace metals)
recognition of the need for more than macromolecules in the diet about 120 years ago
Funk - discovered vital amines
McCollum - discovered fat soluble A and water soluble B
Water-Soluble Vitamins
Dissolve in water
No real stores
Readily excreted
Function: coenzymes & antioxidants
Absorbed by portal system
Not required daily
High doses can be toxic
Subject to cooking & food storage losses
Examples:
B vitamins
Thiamin
Riboflavin
Niacin
Biotin
Pantothenic acid
Vitamin B
Folate
Vitamin C
Fat-Soluble Vitamins
Fat soluble
Stored in tissues
Remain in adipose & liver
Function: hormones, blood clotting, antioxidants
Absorbed by lymphatic system w/ fats (chylomicrons)
Not required daily
High doses can be toxic
Examples:
Vitamin A
Vitamin D
Vitamin E
Vitamin K