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MArishka [77]
3 years ago
11

The malate/aspartate shuttle: if inhibited, could lead to the accumulation of cytosolic glyceraldehyde-3-phosphate within the ce

ll (assume the glycerol-3-phosphate shuttle, LDH, and GNG are not found in this particular cell). if inhibited, would have little to no effect on the flux of GNG (gluconeogenesis). if inhibited, would result in the accumulation of cytosolic NAD (assume the glycerol-3-phosphate shuttle and GNG are not found in this particular cell). D) if inhibited, would result in the accumulation of cytosolic lactate (assume the glycerol-3-phosphate shuttle and GNG are not found in this particular cell). A) and D). A), B), and D). A), B), C), and D).
Biology
1 answer:
AleksAgata [21]3 years ago
7 0

Answer:Recall that the glycolytic pathway generates NADH in the cytosol in the oxidation of glyceraldehyde 3-phosphate, and NAD+ must be regenerated for glycolysis to continue. How is cytosolic NADH reoxidized under aerobic conditions? NADH cannot simply pass into mitochondria for oxidation by the respiratory chain, because the inner mitochondrial membrane is impermeable to NADH and NAD+. The solution is that electrons from NADH, rather than NADH itself, are carried across the mitochondrial membrane. One of several means of introducing electrons from NADH into the electron transport chain is the glycerol 3-phosphate shuttle (Figure 18.37). The first step in this shuttle is the transfer of a pair of electrons from NADH to dihydroxyacetone phosphate, a glycolytic intermediate, to form glycerol 3-phosphate.This reaction is catalyzed by a glycerol 3-phosphate dehydrogenase in the cytosol. Glycerol 3-phosphate is reoxidized to dihydroxyacetone phosphate on the outer surface of the inner mitochondrial membrane by a membrane-bound isozyme of glycerol 3-phosphate dehydrogenase. An electron pair from glycerol 3-phosphate is transferred to a FAD prosthetic group in this enzyme to form FADH2. This reaction also regenerates dihydroxyacetone phosphate.

Explanation:

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Spallanzani's experiments concerning spontaneous generation were NOT universally accepted because __________.
Harrizon [31]

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Explanation:

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3 years ago
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dusya [7]

Answer:

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3 years ago
How do I compare and contrast these?
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3 0
3 years ago
How do doctors and researchers decide whether a disease is a good candidate for gene therapy? what are the advantages and disadv
gladu [14]

Diseases that are best candidates for gene therapy are those whose disorder has been identified to be a malfunctioning gene and the biology of the gene is well known.  Gene therapy is also viable where the proper gene can be correctly delivered and replace the malfunctioned one.

The advantage of using viruses in gene theory is their effectiveness in delivering the desired gene by tapping into their natural mechanisms of infection.  However, disadvantages include the risks of affecting healthy cells while targeting sick cells and wrong placement of the desired gene hence causing undesirable mutations in DNA.

One factor is the length of the DNA that is required to be replaced through gene therapy. Most vectors have a maximum length of DNA that they can carry for effective transduction.  Another is the range of cell types that the vector can infect and the risk of immune response/ allergic reaction/ side effects.

The best vectors are herpes or vaccinia viruses.  The viruses are able to infect non-dividing cells such as the nerve cell. The vectors can accommodate 8400 bp in their genome and the transgene expressions have the potential to last long.

Traditional gene editing techniques such as TALENS and ZFN use modular proteins that target nucleotide sequences. In the CRISPR tool, the Cas9 protein is steered by a guide RNA (which is a complementary sequence to the target sequence) to the target region.

<span>One ethical issue of gene editing is its use in genetic enhancement to develop ‘designer babies’.  The question of who should decide on whether a trait is bad or good also complicates this matter. The morality of artificiality enhancing attributes such as strength, athletic capability, intelligence, and etcetera could lead to an unhealthy ‘arms race’  between humans. </span>

In sports doping, gene editing could be used to enhance genes that enhance muscle strength by targeting myostatin (MSTN) and GF-1 genes. Genes that promote quick break down of lactic acid and increases oxygen capacity of the lungs and blood such as EPO gene could be targets of sports doping.

<span>Gene editing will treat diseases and disorders by repairing the causative defective gene. This is already applicable in cystic fibrosis. Artificial gene selection will be common in future thanks to gene editing.  Future humans will, therefore, have ‘desirable traits’  or new traits depending on what is appealing to the society. </span>


4 0
3 years ago
Which statement is NOT true about subatomic particles?
Alona [7]
It is B I think... this is physical science right?
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3 years ago
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