
Concept explainers
RECALL Proteins,

Interpretation:
The basis for grouping substances such as lipids is to be defined.
Concept Introduction:
Proteins, carbohydrates and nucleic acids are the polymers of amino acid residues, sugar residues and nucleotides, respectively.
Saturated hydrocarbons contain only single-bonded carbon atoms, and unsaturated hydrocarbons contain multiple double or triple bonds.
Electronegativity is the property of an atom to pull electrons towards itself.
Answer to Problem 1RE
Solution:
Lipids are grouped only on the basis of solubility and non-polar nature of their molecules, whereas, some lipids do not share any structural similarity, like, groups if proteins, carbohydrates and nucleic acids.
Explanation of Solution
The amino acid residues are linked together by peptide bonds and polymerize to form a peptide chain, which eventually gives rise to a protein structure. The sugar molecules like glucose are linked together by glycosidic linkages to form a polymer of carbohydrate. DNA (deoxyribonucleic acid) is a polymer of deoxynucleotides, like, adenine, guanine, cytosine, and thymine. Carbohydrates have carbon, hydrogen, and oxygen in their structures. Proteins have amino and carboxyl groups in their structures. The nucleic acids have phosphate, sugar residue and a nitrogenous base in their structures. It suggests that all these molecules are grouped on the basis of some common groups or atoms that are constant in their structure.
The lipids are grouped on the basis of their hydrophobic nature, that is, the fear of water. The lipids are not soluble in water because of the presence of a hydrocarbon chain which is non-polar in nature. Polar molecules are those molecules that contain opposite charges on their molecules, for example, water. In water (
Lipids, sometimes, do not share a common structure. For example, the lipid compounds that carry long hydrophobic hydrocarbon chains and polar head groups are classified as fatty acids, sphingolipids, glycolipids, triacylglycerol, and others. The lipids that contain fused ring structures are grouped as steroids, and cholesterol is the most common type of steroid.
The lipids are grouped on the basis of solubility and non-polar nature. Also, some lipids are not structurally related.
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Chapter 8 Solutions
Biochemistry
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- B- Vitamins are converted readily into important metabolic cofactors. Deficiency in any one of them has serious side effects. a. The disease beriberi results from a vitamin B 1 (Thiamine) deficiency and is characterized by cardiac and neurological symptoms. One key diagnostic for this disease is an increased level of pyruvate and α-ketoglutarate in the bloodstream. How does this vitamin deficiency lead to increased serumlevels of these factors? b. What would you expect the effect on the TCA intermediates for a patient suffering from vitamin B 5 deficiency? c. What would you expect the effect on the TCA intermediates for a patientsuffering from vitamin B 2 /B 3 deficiency?arrow_forwardPyruvate is accepted into the TCA cycle by a “feeder” reaction using the pyruvate dehydrogenase complex, resulting in acetyl-CoA and CO2. Provide a full mechanism for this reaction utilizing the TPP cofactor. Include the roles of all cofactors.arrow_forwardMap out all of the metabolic pathways in the liver cell. Draw out the structures and names of all compounds neatly by hand and the pathways responsible for metabolizing them. Some examples are: Glycolysis/gluconeogenesis, PPP, Glycogenesis/glycogenolysis, Krebs, ETC, selectamino acid pathways (Ala, Glu, Asp) Lipogenesis/lipolysis. Citrate/MAS/glycerol phosphate shuttlesystems, and the Cori/Glc-Ala cycles. Rules:-Draw both a mitochondrial area of metabolism and a cytoplasmic area of metabolism.-Draw the liver and its roles in glucose recycling (Cori cycle/Glc-Alanine recycling)-Avoid drawing the same molecule twice (except for separate mitochondrial/cytoplasmic populations. i.e. Design the PPP/Glycolysis so that GAP is only drawn once)-Label Carbon 4 of glucose and highlight where you would expect to find it in EVERY compound in whichit is present.-Have one or two locations for NADH/NADPH/ATP/GTP/CoQH2 – many arrows will come to/from thesespots.arrow_forward
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- Indicate for the reactions below which type of enzyme and cofactor(s) (if any) would be required to catalyze each reaction shown. 1) Fru-6-P + Ery-4-P <--> GAP + Sed-7-P2) Fru-6-P + Pi <--> Fru-1,6-BP + H2O3) GTP + ADP <--> GDP + ATP4) Sed-7-P + GAP <--> Rib-5-P + Xyl-5-P5) Oxaloacetate + GTP ---> PEP + GDP + CO26) DHAP + Ery-4-P <--> Sed-1,7-BP + H2O7) Pyruvate + ATP + HCO3- ---> Oxaloacetate + ADP + Piarrow_forwardThe phosphate translocase is an inner mitochondrial membrane symporter that transports H2PO4- and H+ into the mitochondrial matrix. Phosphate is a substrate for Complex V (the ATP Synthase), the enzyme that couples the synthesis of ATP to the H+ gradient formed by the electron transport chain. (a) Bongotoxin is a hypothetical compound that inhibits the phosphate translocase of the inner mitochondrial membrane. Explain why electron transport from NADH to O2 stops when bongotoxin is added to mitochondria (i.e., why do electrons stop flowing through the electron transport chain even with an abundance of NADH and O 2 present). What effect will the addition of the weak acid dinitrophenol (DNP) to the cytosol have on electron transport in bongotoxin-inhibited mitochondria? Be sure to explain your answers. (b) How much free energy is released (in kJ) when one mole of protons flows from the mitochondrial inner membrane space (IMS) to the mitochondrial matrix when the [H+ ] in the IMS is 7.9 x…arrow_forwardWhen TMPD/ascorbate is added to mitochondria as a source of electrons (TMPD/ascorbate reduce cytochrome c directly) oxygen is reduced to H2O by the electron transport chain (ETC).(a) Approximately how many ATPs would result per O2 consumed when electrons come from TMPD/ascorbate? (b) If dinitrophenol (DNP) is added to the mitochondria in (a) above, what effect would DNP have on the yield of ATPs per O2 reduced from TMPD/ascorbate electrons?arrow_forward
- BiochemistryBiochemistryISBN:9781305961135Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougalPublisher:Cengage Learning
