所屬科目:研究所、轉學考(插大)◆生物化學
1._______received the Nobel prize in 1954 for his discovery of the protein secondary structures (a helix and β sheet). (A) Walter Gilbert (B) Erwin Chargaff (C) Linus Paulin (D) Fred Sanger (E) Karst Hoogsteen
2. αhelix of a polypeptide has a pitch (height per turn) of ______m. (A) 0.10 (B) 0.15 (C) 0.34 (D) 0.54 (E) 1
3. Which of the following descriptions about Hb (hemoglobin) is incorrect? (A) One Hb can bind 4 O2 molecules (B) HbA has an a2β2 structure (C) HbF has an α2γ2 structure (D) HbF has a higher affinity for BPG than does HbA(E) CO2 reduces the binding affinity of Hb for O2.
4.Which of the following descriptions about the Michaelis-Menten rate equation is incorrect? (A) KM measures the substrate concentration at which the reaction rate is Vmax/2 (B) kcat is the turnover number that measures the rate of the catalytic process (C) The ratio of kcat/Vmax is a convenient measure of enzyme efficiency (D) The unit for KM is μV (E) The unit for kcat is s-1.
9. Which of the following descriptions regarding disaccharide is incorrect? (A) Sucrose is α-D-glucopyranosyl (1-2) β-D-fructopyranoside (B) Sucrose is a non-reducing sugar (C) Maltose has an a(1→4) linkage (D) Cellobiose is β-D-glucopyranosyI (1→4) β-D-glucopyranose (E) Lactose is a reducing sugar.
17. Which of the following bond-pairs within a peptide backbone show free rotation around both bonds? (A) N-Cu and N-C (B) Cα-C and N-Cα (C) C=O and N-C (D) C=O and N-Ca (E) N-C and Cα-C.
22. Which of the following tautomeric forms is the major form of ribose in solution? (A) α-pyranose (B)β-pyranose (C) α-furanose (D) β-furanose (E) all of the above.
28. Which of the following reactions is not located in mitochondria? (A) tricarboxylic acid cycle (B) electron transport (C) gluconeogenesis (D) β-oxidation (E) oxidative phosphorylation.
37.n a supercoiled DNA, a stretch of ~20 base pairs changes from the B form to the Z form. △W =________ .(A)+1.7(B)+2.7(C)+3.7 (D) -1.7 (E) -3.7
40. Only the________tautomeric form of ribose exists in the nucleic acid structure? (A)α-pyranose (B) β-pyranose (C) α- furanose (D) β-furanose (E) all of the above.