As a Scientist, I get asked many questions as I am sure you understand. Of course I have to protect my identity. I allow the mundane world to address me as Dr. Nucleus. The nucleus being the heart of the atom, I found that title particularly (pun intended) fitting. The following is the greatest thing I know and sharing it with the world (and now you) is the greatest thing I have done.
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Dear Doctor Nucleus,
Although I want to become a great Scientist like you, I don't have the money or grades to attend some prestigious institution for years to get my degree. Help me, please! How can I get the Scientific education that I want and need?
Concernedly,
Edward Showen Teller
Dear Teddy,
A Scientist does not need a highfalutin university to confer some worthless scrap of ram's epidermis upon him. To a Scientist candidate, the whole world is an education.
If your time is limited, the most direct route to greatness would be home study. Get up late in the afternoon, mornings are for non-Scientists, and brew yourself a pot of triple strength coffee. Drink it all; Science has no half measures. Time for breakfast! Stock up on Captain Crunch, Twinkies, and more coffee. Now stare into the mirror and chant, "Science is Truth -- Truth is Science" for about an hour. This will get you close to the mind state where your brain is ready to receive great Truths.
Find a TV station showing movies about great Scientists, preferably those of Bert I. Gordon ("The Amazing Colossal Man" and "Earth Vs. the Spiders”.) Set an electric fan, turning at precisely 60 rpm, in front of the screen and watch the movie through the turning blades. This stroboscopic effect simulates "cat naps" which all great Scientists must take. Sleepy? Time for more coffee and, for health reasons, microwave popcorn.
Be a Scientist, act the part! Write down all observations in steno notebooks. Mutter to yourself. In bookstores' Science sections, fling books off shelves and scream "Lies! Lies! Damnable lies!" Soon you will get the respect you deserve.
Scientifically,
Dr. Nucleus
2006-06-16 03:46:10
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answer #1
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answered by NeoArt 6
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1. Kreb’s Cycle
Glycolysis:
6C glu à 3C pyruvate x2
Glu + 2NAD+ + 2 ADP + 2 Pi à 2 pyr + 2 NADH + 2 H+ + 2 ATP + 2 H2O
D Go’ = -85 kJ/mole
2 NADH à e- transport à ATP synth (16-1)
In cytosol
3C Pyruvate Product
2 C’s added to Coenzyme A (CoA)(16-3)
As acetate group
Activates CoA (thioester)
1 C as CO2
Pyruvate Dehydrogenase
Complex (PDC)
Catalyzes acetylation CoA (16-2)
Oxidative decarboxylation (LEO + cleave carboxylate)
In mitochondria
3 associated enz’s
Pyruvate dehydrogenase
Dihydrolipoyl transacetylase
Dihydrolipoyl dehydrogenase
5 cofactors
PDC E1: Pyruvate Dehydrogenase
24 copies in complex (E. coli)
Cofactor: thiamine pyrophosphate (TPP) (15-9)
PDC E1: Pyruvate Dehydrogenase
Pyr binds à ethanolic grp att’d to TPP
CO2 released
Ox’n to acetaldehyde w/ transfer to E2
PDC E2: Dihydrolipoyl
Transacetylase
"Core" of complex
24 copies (E. coli)
Cofactor: lipollysyl (16-4)
Molecular "arm"
In ox’d form – 5 membered ring w/ disulfide
Ethanolic grp att’s here, ox’d à acetaldehyde
-S-S- red’d to –SH HS- w/ ox’n to acetaldehyde
Thioester
Site of attack by CoASH
Transesterification
à AcetylCoA + dithiol lipoyl
PDC E3: Dihydrolipoyl
Dehydrogenase
12 copies att’d to E2 (E. coli)
Cofactor: FAD
REMEMBER: Flavin nucleotide cofactors bound to enz’s
Nicotinamide nucleotides cofactors freer to dissociate
Used to reoxidize lipollysyl
FAD red’d à FADH2
Lipollysyl ox’d à ring w/ disulfide
FADH2 regen’d by NAD+ entry
FADH2 ox’d à original FAD
NAD+ red’d à NADH
Leaves complex
Where might it go?
PDC Summary
3 Enz’s closely assoc’d
Acetyl grp physically transferred
Regulatory
Both allosteric + covalently modified regulation
E1 has kinase, phosphatase enz’s assoc’d
Kinase phosphorylates, inactivates
Phosphatase dephosphorylates, activates
Assoc’d kinase allosterically controlled
ATP stimulates
Act’d kinase inactivates PDC
So  [ATP] à ?? PDC??
Modulators (16-15)
Inhibitory: ATP, NADH, acetyl CoA, fatty acids
Why??
Stimulatory: ADP/AMP, NAD+, pyruvate, CoA
Why??
Kreb’s Cycle
= Citric Acid Cycle = Tricarboxylic Acid Cycle = TCA Cycle (16-11,16-7)
2 C’s from pyr (as acetyl on acetylCoA)
2 C’s leave as CO2 (not same 2 C’s that entered)
4 redox rxn’s
3 NAD+ Ã 3 NADH; 1 FAD Ã FADH2
Where will these go?
1 high energy phosphate bond formed
1 GDP Ã 1 GTP (some cells 1 ADP Ã 1 ATP)
REMEMBER the name of this phosph’n?
Oxaloacetate regen’d
REMEMBER: 2 turns for each glu
Up to 38 ATP/glu (>1160 kJ/mole avail)
1 step uses complex sim to PDC
Acetyl CoA + Oxaloacetate
à Citrate + CoASH
Citrate Synthetase
Condensation rxn
CoASH regen’d
Through CH3 of acetyl
Transient intermediate: citroyl CoA (p.573)
Energy rel’d from cleavage acetylCoA
Why? What grps impt to exergonic rxn?
Oxaloacetate binds first (16-8)
à Conform’l change
Now site for acetylCoA
Modulators (16-15)
Availability of substrates
Inhib’n w/ Â [citrate]
What type of inhib’n?
 [citrate] also inhibits PFK-1
Where is PFK-1?
What type of inhib’n would this be?
Inhib’n w/ Â [ATP]
Relieved w/ Â [ADP]
Why?
Inhib’n w/ Â [succinyl CoA]
Feedback inhib’n
Citrate à Isocitrate
Aconitase
Isomerization
Cis-aconitate intermediate
Iron-sulfur center (16-9)
Isocitrate à a Ketoglutarate
+ CO2
Isocitrate Dehydrogenase
Ox’n rxn
NAD+ or NADP+ depending on isozyme
Regulation (16-15)
Inhib’n w/ Â [ATP]
Inhib’n w/ Â ratio [NADH]/[NAD+]
Why?
a Ketoglutarate Ã
SuccinylCoA + CO2
a Ketoglutarate
Dehydrogenase Complex
Identical rxn to PDC
Similar E1, E2, E3 enzymes
Same cofactors
NAD+
Regulation (16-15)
Inhib’n w/ Â [succinyl CoA]
Inhib’n w/ Â ratio [NADH]/[NAD+]
SuccinylCoA Ã
Succinate + CoASH
SuccinylCoA Synthetase (16-10)
+ Pi à high energy acyl phosphate intermediate in enz active site + CoASH released
Phosphate transferred to enz active site His
GDP enters active site; phosph’d à GTP
Substrate level phosph’n results
Book: GTP formed transfers PO4 to ADP later
Succinate à Fumarate
Succinate Dehydrogenase
Membr-bound
Euk’s – inner mitoch membr
Prok’s – plasma membr
Impt also in e- transport
FAD may be cov’ly bound
Fumarate à L-Malate
Fumarase
Hydration trans across db
Enz stereospecific
L-Malate à Oxaloacetate
L-Malate Dehydrogenase
Substrate limited rxn
Large + D G
Why does the rxn go?
Cycle
Complete w/ regen’n oxaloacetate
Amphibolic
Impt to both catabolism (breakdown) and anabolism (build-up) of cell’s molecules
Catabolism of carbohydrates, FA’s, aa’s through pyruvate, acetylCoA(17-8; 18-14) à Kreb’s à ATP
Anabolism by cycle intermediates à aa’s, fa’s, lipids, purines/pyrimidines (16-13)
Balance of amphibolic pathways through anapleurotic rxns (16-13)
Replenish cycle intermediates so TCA remains constant
4 impt rxns (Table 16-2)
Synth oxaloacetate or malate from pyruvate or phosphoenolpyruvate
Where did you see these reactants?
If    glycolysis (so    PEP/pyr products), but not enough oxaloacetate to fuel cycle
Cell can use excess PEP/pyr to make more oxaloacetate
Now have sufficient to react w/ excess acetylCoA (from excess pyr, from excess PEP)
2. Love someone with all my heart and passion
2006-06-15 23:19:46
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answer #2
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answered by Pammie 2
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i know the greatest that we will respect our mother father and teacher and our nation .the greatest thing i done that i consider my god is father and mother
2006-06-15 23:18:23
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answer #3
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answered by Anonymous
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Nothing is the greatest thing..and i did nothing that is the best part!!!!!!!! lol
2006-06-16 16:29:12
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answer #4
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answered by Anonymous
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1)newtons 3rd law-every action has a equal and opposite reaction.
and about DNA .......it controls everything
2)i love and trust my parents and my friends.coz trust is important in any relationship.....
2006-06-16 00:37:51
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answer #5
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answered by life is beautiful 2
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That Jesus Christ died for me!!!
Accepted Jesus as my Savior!!!!
2006-06-15 23:15:19
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answer #6
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answered by gentlemanfarmer 3
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