Explanation:
Eukaryotic cells have specialized mechanisms to transport molecules along with membrane-bound organelles like the endoplasmic reticulum that provide a higher surface area for absorption and enable more efficient transportation.
Their structural components (i.e. their makeup) determine their function (what they do). In specific cell types, collected proteins may function as a unit called an organelle. Some organelles are bound by membranes like those that make up the external structure of the cell, with varying compositions of phospholipids and proteins. Several organelles facilitate the digestion of nutrients into metabolites and energy...
- Step 1: Mitochondria break down food and release energy; In all eukaryotic cells mitochondria are small cellular organelles bound by membranes. The higher concentrations of reactants and solutes, increases metabolic reaction efficiency; these make most of the chemical energy required for powering the biochemical reactions within the cell. This chemical energy is obtained via the breakdown of nutrients from food, and is stored within the molecule ATP. Respiration in the mitochondria utilizes oxygen for the production of ATP in the Krebs’ or Citric acid cycle via the oxidization of pyruvate (through the process of glycolysis in the cytoplasm) where several metabolites used for building other compounds are produced.
- Step 2: Lysosomes... Some organelles separate proteins and molecules that may harm the cell by parceling them into membrane-bound organelles for example, proteases bound within lysosomes can break down many structural proteins, and carbohydrates found in food, waste, and cell components
- Step 3: Vacuoles... Vacuoles are fluid filled organelles which store concentrated amounts of solutes, and waste products. Specialized vacuoles are also used to transport components to the cell membrane for cellular export.
- Step 4: The endoplasmic reticulum... Most proteins that function in the cytosol (such as actin) or in the nucleus (such as DNA polymerase) are synthesized by free ribosomes. Proteins that function within the endomembrane system (such as lysosomal enzymes) or those that are destined for secretion from the cell (such as insulin) are synthesized by bound ribosomes in the rough endoplasmic reticulum. The rest of the ER, which does not contain ribosomes is called the smooth ER, and may contain lipids, enzymes, and other proteins. As a protein destined for the endomembrane system is being synthesized by a ribosome, the first amino acids in the growing polypeptide chain act as a signal sequence. That signal sequence ensures that the ribosome binds to the outer membrane of the ER and that the protein enters the ER lumen.
- Step 5: Golgi bodies... Like a post office, the golgi complex, or golgi body recognizes signal sequences and packages these compounds into lysosomes for delivery to their final destination. Lysosomes fuse with the plasma membrane to empty their contents into the extracellular space.
Learn more about cellular life at brainly.com/question/11259903
Learn more about mitochondria at brainly.com/question/8427362
Learn more about mitochondria and similar structures at brainly.com/question/2855039
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Answer: Burning of paper
•Burning of candle
•Earthquakes
•Thundering
•Lightning
hope that helped :) get i get brainliest?
Explanation:
<span>The cell uses oxygen to break down glucose which releases energy. This energy is stored in the form of ATP.</span>
Answer:
Answer is C.
Explanation:
For A and B, a base substitution affects one of the three bases that comprise a codon, the DNA/RNA unit that corresponds to a particular amino acid. If one base is substituted, one codon and therefore one amino acid will be affected. Codons have built-in redundancy, so even by changing one base, the new codon sometimes still corresponds to the same amino acid. Therefore, a base substitution at most affects one amino acid, and sometimes doesn't affect it all.
Frameshift mutations cause a lot more trouble. These occur when you have a deletion or insertion that changes the number of bases in your gene. As a result, the "frame" of the codons changes (everything shifts one way or the other by the number of bases added/removed). This affects EVERY codon downstream of the mutation, so you can imagine that such a mutation would have a bigger effect the closer to the start of the gene it occurs. This is why C is correct.
