This document is the WGU BioChem OA Review with Complete and Verified Solutions, a comprehensive biochemistry objective assessment study guide containing exam-style questions with verified answers covering the full scope of WGU biochemistry. The content includes molecular biology techniques such as Polymerase Chain Reaction (PCR), its three steps of denaturing, annealing, and elongating, the required components of template DNA, nucleotides (dNTPs), DNA polymerase, and DNA primers, and what is not involved in PCR; DNA repair mechanisms including base excision repair (BER) with glycosylases, DNA polymerase, and DNA ligase, mismatch repair (MMR) during replication and proofreading, nucleotide repair for UV damage, homologous recombination for double-stranded breaks, and non-homologous recombination leading to frameshift mutations; DNA transcription, RNA splicing where introns are removed and exons joined, gene expression, epigenetics, and DNA packaging into nucleosomes and chromatin; mutation types including nonsense mutations producing premature stop codons, silent mutations with no phenotypic effect, and missense mutations coding for different amino acids; inheritance patterns including autosomal dominant and autosomal recessive conditions, X-linked dominant disorders, heterozygous and homozygous genotypes, and the inheritance of sickle cell anemia with the GAG to GUG change in hemoglobin; amino acid chemistry including polar, non-polar, ionized amino acids, hydrophobic and hydrophilic side chains, and what happens when alanine loses an electron; protein structure and misfolding including the four levels of protein structure (primary, secondary, tertiary, quaternary), what determines the 3D shape of a protein, secondary structure beta sheets and alpha helices, denaturing, molecular chaperones, protein aggregation, and the role of amyloid-beta and TAU protein in Alzheimer's disease, plus neurodegenerative protein aggregation in Parkinson's, Huntington's, ALS, and prion diseases; enzyme kinetics including substrates, substrate-enzyme complexes, active sites, allosteric sites, competitive and non-competitive inhibitors, feedback inhibition, and how methotrexate treats cancer; metabolic pathways including the citric acid cycle, acetyl CoA, NADH and FADH2, fermentation, anaerobic glycolysis, the Cori cycle, substrate-level phosphorylation, glycogenesis, glycogenolysis, gluconeogenesis, glycolysis, glycation, glucose and glycogen, and how glucagon and insulin regulate carbohydrate metabolism, plus GluT4 and metformin; lipid and fatty acid metabolism including beta oxidation in the mitochondria, fatty acid synthesis in the cytoplasm, saturated versus unsaturated fats, CIS and TRANS configurations, omega-3 and omega-6 fatty acids, triglycerides, eicosanoids, phospholipids, the fluid mosaic model, cholesterol structure and function, and MCAD deficiency with its dietary management; hemoglobin and oxygen transport including cooperative binding, carbon monoxide poisoning, 2,3-BPG, the tense and relaxed states of hemoglobin, the difference between hemoglobin and myoglobin affinity, the Bohr effect, and how pH and CO2 influence oxygen saturation; and clinical correlations including myoglobin and troponin in myocardial infarction, LDL and high cholesterol, and the CHART mnemonic for low pH, high carbon dioxide, high hydrogen, acidic, right shift, and tense state.
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WGU BioChem OA Review with
Complete and Verified Solutions
Males and Females are equally affected ✔✔Autosomal
The process of copying DNA in the lab. ✔✔Polymerase Chain Reaction (PCR)
Template DNA, Nucleotides (dNTPS), DNA Polymerase, and DNA Primers. ✔✔What is needed
for Polymerase Chain Reaction?
Denaturing, Annealing, Elongating ✔✔What are the three steps of a Polymerase Chain Reaction
(PCR)?
Denaturing (DNA is heated up to separate it) ✔✔What is the first step of a Polymerase Chain
Reaction?
Cooling the Polymerase Chain Reaction. Primers stick to the DNA that you want to copy and ADD
DNA Polymerase ✔✔What is Annealing?
The Polymerase Chain Reaction is heated and DNA Polymerase adds nucleotides to build a new
DNA strand. ✔✔What is elongating?
,Ligase ✔✔What is NOT involved in PCR?
It is used to repair damage to bases caused by harmful molecules by removing the base that is
damaged and replacing it. #1 GLYCOSYLASES see the damaged DNA. #2 DNA Polymerase puts
the right one back #3 DNA Ligase seals it. ✔✔What is base excision repair (BER)?
DNA Glycolysase sees the damage and removes it, DNA polymerase puts the tight base back,
DNA ligase seals it back up. ✔✔What are the 3 steps in base excision repair?
1 ✔✔How many nucleotides does base excision repair remove?
Mismatch Repair (MMR). It is the only one to occur during REPLICATION - DURING THE
PROOFREADING ✔✔What is it called when a large section of the nucleotide is removed from
the DNA so that DNA polymerase can try again? (This corrects DNA damage)
Mismatch Repair (MMR) repairs errors such as G with T instead of G with C. DNA Polymerase
fixes it. This happens during replication and MMR removes a large section of the nucleotide from
the DNA and DNA Polymerase tries again. ✔✔What repairs a base mismatch?
When DNA polymerase takes an individual nucleotide and matches them to the parental sequences
to ensure a correct pair. (it must bind with RNA primer to work). ie: DNA Polymerase binds to
DNA to make RNA ✔✔What is DNA Transcription?
, CLEANS damage caused by things such as UV rays and repairs it. A large section of nucleotides
are removed, including the damaged portion, along with a few on each side. It is then replaced by
DNA polymerase. ✔✔What is NecleoTIDE repair
It repairs double stranded breaks (last effort) by copying another strand of DNA and replacing it
completely. ✔✔What is Homologous Recombination?
Another last effort to repair a double strand break by putting the ends back together before making
sure they are correctly copied. This can lead to deletions/insertions (frameshift mutations).
✔✔What is Non-Homologous Recombintaion?
It must bind to RNA primer ✔✔What does DNA Polymerase bind to in order to make RNA
TRANSCRIPTION DNA take the individual nucleotide and match them to the PARENTAL
sequences to ensure a correct pair.
introns (non-coding region) are removed and exons (coding region) joined to form a contiguous
coding sequence. ✔✔What happens during RNA splicing to generate a mature RNA molecule?
The ability to turn genes on and off ✔✔What is Gene Expression?