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Biochemistry

Latest questions in this category.

27 questions

Lyophilization is a method used for preservation of microbes because:

Mechanistically, enzyme catalysis and lipid structure involves substrate affinity, transition state stabilization and phospholipid composition govern function. This validates moisture is removed by sublimation because it reflects catalytic efficiency and membrane organization, a pattern repeatedly demonstrated in biochemistry research.

Ref: Lehninger Principles of Biochemistry, Chapter 9, Lipids and Membranes, explains phospholipid components, glycerol, fatty acids, phosphate group and membrane structure providing foundation for lipid biochemistry.

IPTG is used as an inducer in the T7 expression system for recombinant protein expression in E.coli. This is because of:

Mechanistically, enzyme catalysis and lipid structure involves substrate affinity, transition state stabilization and phospholipid composition govern function. This validates availability of special E.coli cells which have the T7 RNA polymerase gene in... because it reflects catalytic efficiency and membrane organization, a pattern repeatedly demonstrated in biochemistry research.

Ref: Berg, Tymoczko, Gatto and Stryer, Biochemistry, 9th Edition, Chapter 13, Metabolism and Bioenergetics, covers glycolysis, citric acid cycle, oxidative phosphorylation and NADH-linked reactions detailing biochemical principles of cellular energy metabolism.

Which one of the following eIF2α kinases get activated during unfolded protein response (UPR) in mammalian cells?

The principle of enzyme catalysis and lipid structure explains that substrate affinity, transition state stabilization and phospholipid composition govern function. Hence PERK fits best because it reflects catalytic efficiency and membrane organization, as documented in authoritative sources on biochemistry.

Ref: Lehninger Principles of Biochemistry, Chapter 9, Lipids and Membranes, explains phospholipid components, glycerol, fatty acids, phosphate group and membrane structure providing foundation for lipid biochemistry.

The gene encoding an enzyme A that functions in a metabolic pathway for conversion of metabolite „x‟ to „y‟ was knocked

Mechanistically, enzyme catalysis and lipid structure involves substrate affinity, transition state stabilization and phospholipid composition govern function. This validates Enzyme A is sufficient but not necessary for formation of „y‟ because it reflects catalytic efficiency and membrane organization, a pattern repeatedly demonstrated in biochemistry research.

Ref: Nelson and Cox, Lehninger Principles of Biochemistry, 7th Edition, Chapter 6, Enzyme Kinetics and Regulation, discusses Michaelis-Menten equation, transition state stabilization and allosteric control supporting enzyme function and metabolic regulation.

Glycosylation of membrane proteins and lipids is carried out by enzymes present in the lumen of endoplasmic reticulum an

The principle of enzyme catalysis and lipid structure explains that substrate affinity, transition state stabilization and phospholipid composition govern function. Hence Exposed to the extracellular environment fits best because it reflects catalytic efficiency and membrane organization, as documented in authoritative sources on biochemistry.

Ref: Lehninger Principles of Biochemistry, Chapter 9, Lipids and Membranes, explains phospholipid components, glycerol, fatty acids, phosphate group and membrane structure providing foundation for lipid biochemistry.

In human carcinomas, many proteins including most cytoskeletal proteins undergo modifications, thereby making it difficu

In biochemistry, enzyme catalysis and lipid structure dictates that substrate affinity, transition state stabilization and phospholipid composition govern function. Therefore Intermediate filament is correct as it reflects catalytic efficiency and membrane organization, supported by mechanistic studies and conserved across related systems.

Ref: Berg, Tymoczko, Gatto and Stryer, Biochemistry, 9th Edition, Chapter 13, Metabolism and Bioenergetics, covers glycolysis, citric acid cycle, oxidative phosphorylation and NADH-linked reactions detailing biochemical principles of cellular energy metabolism.

In humans, the enzyme having reverse transcriptase activity is:

enzyme catalysis and lipid structure analysis shows substrate affinity, transition state stabilization and phospholipid composition govern function. Consequently Telomerase emerges as the valid choice since it reflects catalytic efficiency and membrane organization, aligning with established principles in biochemistry literature.

Ref: Nelson and Cox, Lehninger Principles of Biochemistry, 7th Edition, Chapter 6, Enzyme Kinetics and Regulation, discusses Michaelis-Menten equation, transition state stabilization and allosteric control supporting enzyme function and metabolic regulation.

One of the reasons why non-substrate inducers (e.g. IPTG) are preferred over substrate inducers (e.g. lactose) for induc

Mechanistically, enzyme catalysis and lipid structure involves substrate affinity, transition state stabilization and phospholipid composition govern function. This validates They directly interact with the repressor because it reflects catalytic efficiency and membrane organization, a pattern repeatedly demonstrated in biochemistry research.

Ref: Lehninger Principles of Biochemistry, Chapter 9, Lipids and Membranes, explains phospholipid components, glycerol, fatty acids, phosphate group and membrane structure providing foundation for lipid biochemistry.

Which of the following signatures (the stretch of amino acids) in a protein will target it to the nucleus?

This outcome reflects enzyme catalysis and lipid structure, where substrate affinity, transition state stabilization and phospholipid composition govern function. Option B captures this correctly because it reflects catalytic efficiency and membrane organization, consistent with textbook descriptions and experimental observations in biochemistry.

Ref: Berg, Tymoczko, Gatto and Stryer, Biochemistry, 9th Edition, Chapter 13, Metabolism and Bioenergetics, covers glycolysis, citric acid cycle, oxidative phosphorylation and NADH-linked reactions detailing biochemical principles of cellular energy metabolism.

Amino acids with asymmetric Cβ atoms are:

The principle of enzyme catalysis and lipid structure explains that substrate affinity, transition state stabilization and phospholipid composition govern function. Hence Thr, Ile fits best because it reflects catalytic efficiency and membrane organization, as documented in authoritative sources on biochemistry.

Ref: Nelson and Cox, Lehninger Principles of Biochemistry, 7th Edition, Chapter 6, Enzyme Kinetics and Regulation, discusses Michaelis-Menten equation, transition state stabilization and allosteric control supporting enzyme function and metabolic regulation.

The α-helix in a protein is primarily due to:

This outcome reflects enzyme catalysis and lipid structure, where substrate affinity, transition state stabilization and phospholipid composition govern function. Option A captures this correctly because it reflects catalytic efficiency and membrane organization, consistent with textbook descriptions and experimental observations in biochemistry.

Ref: Lehninger Principles of Biochemistry, Chapter 9, Lipids and Membranes, explains phospholipid components, glycerol, fatty acids, phosphate group and membrane structure providing foundation for lipid biochemistry.

Protein kinases phosphorylate proteins at hydroxyl groups on amino acid side chains. Which one of the following groups o

In biochemistry, enzyme catalysis and lipid structure dictates that substrate affinity, transition state stabilization and phospholipid composition govern function. Therefore Serine, threonine and tyrosine is correct as it reflects catalytic efficiency and membrane organization, supported by mechanistic studies and conserved across related systems.

Ref: Nelson and Cox, Lehninger Principles of Biochemistry, 7th Edition, Chapter 6, Enzyme Kinetics and Regulation, discusses Michaelis-Menten equation, transition state stabilization and allosteric control supporting enzyme function and metabolic regulation.