Essay On Lysosome

The main function of the mitochondria is to convert fuel into a form of energy the cell can use. Specifically, the mitochondria is where pyruvate --derived from glucose-- is converted into ATP (Adenosine triphosphate) through cellular respiration. Cellular respiration involves four stages: glycolysis, the grooming phase, the citric acid cycle, and oxidative phosphorylation. The final two stages listed occur in the mitochondria.

Mitochondrion function is to produce energy from sugar. This is parallel to a restaurant inside a hospital. The employees eat (carbohydrates) from the hospital restaurant and then their bodies convert it to energy.

3. State the name and structure of the functional group for each type of biologically

Mitochondria, dubbed the ‘powerhouse of the cell’, are a type of organelle present in most human cells. Their primary function is to generate Adenosine Triphosphate (ATP), the cell’s principal source of chemical energy. Unlike most other organelles, mitochondria store their own set of genetic material, distinct from the DNA situated in a cell’s nucleus. Although this ‘mitochondrial genome’ represents only 0.1% of a cell’s genetic information, it often plays a significant role in development.

1. The feature that most clearly separates eukaryotes from prokaryotes is the presence of _______ in eukaryotic cells.

Background Research: Cellular Respiration is used by the cells to make ATP, by releasing chemical energy from sugars and other carbon based molecules. There are 3 stages to Cellular Respiration, Glycolysis, Krebs Cycle, and the Electron Transport Chain. The inputs of Glycolysis are 2 ATP’s, a Glucose molecule, and a Pyruvate. The inputs for the Krebs Cycle are oxygen, and. In animals, energy is consumed by eating food. In that food they eat, Glucose is found and broken down by the process of cellular respiration, which then converts into energy known as ATP. When there is a lot of ATP and Glucose, the liver converts it into glycogen.

PINK1 (PTEN Induced Putative Kinase 1) is a gene that provides directions for making the protein PTEN induced putative kinase 1. The greatest amounts of this protein can be found in the muscles, heart, and testes, but it is also found in cells throughout the body. The protein lies within the mitochondria of the cell, and, although the function of PTEN induced putative kinase 1 is not yet fully understood, it seems to assist in protecting the mitochondria from becoming impaired when the cell is under stress. In order for PTEN induced putative kinase 1 to help the mitochondria, it needs to first function properly itself. Two specialized regions of this protein ensure that it does this. One of these regions, the mitochondrial targeting motif, serves as the delivery address. In other words, once the protein is created, the mitochondrial targeting motif makes sure that it gets to the mitochondria. The other region, the kinase domain, most likely executes the proteins protective function.

The mitochondria has been known as the powerhouse of the cell. What does that even mean? Well, what it means that the mitochondria does all of the cell energy conversion. It takes nutrients from the cell and transforms it into viable ATP. ATP, molecule adenosine triphosphate, is the energy that cells can use. The process in turning nutrients into ATP is called ATP Synthase. The first part of ATP synthase is an ending of cellular respiration. The mitochondria plays a small but large role in the cell. The structure of the mitochondria plays a huge part of cellular respiration. Mitochondrial structure has two membranes an inner and an outer. Inside the inner membrane you have the matrix and the cristae. The first part of cellular respiration is glycolysis, it is made outside of the mitochondria in a gel like fluid called the cytoplasm. Next, is the citric acid cycle, also known as the Krebs cycle, named after the German researcher Hans Krebs, goes in through the outer membrane. Enzyme Acetyl CoA enters and combines the two carbon groups with another four carbon groups. The result is six carbon molecules citrate, which are acidic. The next part in the Krebs cycle is that the hydrogen atoms are stripped and produce NADH molecules. The final Krebs step is; ADP is transferred to ATP the succinate is oxidized forming another four carbon molecule. The two hydrogen carbons react and their electrons transform from FAD to FADH2. The Krebs cycle makes only about 4 ATP and in the

The mitochondria is known as the “power house” of a cell that functions at the site of respiration. Within the inner membrane, ATP synthesis occurs which provides energy to the cell and it other parts. Without function of a mitochondria, a cell would die; it has no energy to repair itself, has no energy to transport molecules across the membrane, transport nutrients, send signals to other cells, or any other processes. Metabolism, release of energy, movement, or forming new nucleotides would not occur simply because energy is not available.

Mitochondrial cytopathy is a genetic heritable disorder [5]. It occurs as a result of DNA mutation in the gem-line cells that can be transmitted to the second generation. This type of genetic disorder is often caused by mutations in the mitochondrial DMA versus the nucleic DNA. The mitochondria DNA is 20-30 times more susceptible to acquire mutations secondary to absence of DNA repair mechanisms in the mitochondria, giving rise to frequent point mutations or deletions in the mtDNA during cell division[1]. Such mutations are inherited exclusively from the maternal mitochondria. The paternal mitochondria do not contribute to the fetal mitochondria [6]. When some of the mitochondria in the ovum have mutations in their DNA, some of those defected mitochondria will go to daughter cells upon division. If the cells receiving the defected mtDNA contribute to forming tissues that are actively dividing after birth, they will be eliminated by the natural selection process after successive cell divisions. In contrast, if the cells inheriting the defected mitochondria developed into organs or tissues of limited dividing ability, this will result in problems related to energy metabolism in that organ [6]. Due to the random nature of the process, defected mitochondria may end up randomly in different types of tissue and at different concentration. This explains the variations in the manifestation, progression, prognosis and severity of the disorder.

Eukaryotic cells produce the chemical energy they need through the processes of either oxidative phosphorylation or photophosphorylation. Oxidative phosphorylation is the last step in the process of cellular respiration and accounts for nearly 90% of ATP production during cellular respiration. During stage one of cellular respiration 2 ATP molecules are broken down to provide the energy necessary to start glycolysis. Each glucose molecule is broken down into 2 pyruvate molecules and 4 ATPs are formed. A net gain of two ATPs is realized. In stage two the pyruvate molecules enter into the mitochondrion of the cell. The pyruvate molecules are oxidized into the compound acetyl CoA. In stage three, the acetyl CoA passes into citric acid cycle (Krebs

This would mean that the cells that require a lot of energy however would not get it, which would result in tiredness, fatigue and the body not functioning efficiently. Also, diseases that affect the mitochondria can affect the functions and cause death of many numbers of cells which can damage the vital internal organs and the body as entirety. We would not live if all the mitochondria in the liver cell were to be destroyed. As mitochondrion is known as the power house of energy, it provides energy to it. The electron micrograph shows the rough endoplasmic reticulum and mitochondria of a liver cell. It also shows there are a lot of mitochondria in the liver cell because the body arranged this specific organ to do perform a variety functions. The reason why liver cells have a high number of mitochondria is because it has to get a lot of energy at one time in order to be more efficient. The liver itself is the largest internal organ in the whole body and hence requiring a large amount of mitochondria to perform at a suitable, appropriate and efficient level. Being the largest organ, it is necessary for it to have a significant amount of mitochondria as it needs a tremendous amount of energy or it shall stop functioning and problems will arise like liver

The hub of energy metabolism, the mitochondrion, is found in virtually all eukaryotic cells, with the exception being erythrocytes. The mitochondrion generates cellular energy in the form of adenosine triphosphate (ATP), mostly by means of the oxidative phosphorylation (OXPHOS) system that is located in the inner mitochondrial membrane. The respiratory chain (CI-CIV) and ATP synthase (CV) is collectively known as the OXPHOS system, encoded by both nuclear DNA (nDNA) and mitochondrial DNA (mtDNA). The number of mitochondria per cell, ranging from hundreds to thousands, is controlled by the energy requirements of specific tissues with the greatest abundance of mitochondria found in metabolic active tissue (Pieczenik and Neustadt, 2007). Mitochondrial disease is caused when there is a defect in any of the numerous mitochondrial pathways, due to spontaneous or inherited mutations. Respiratory chain deficiencies (RCDs) are the largest subgroup of mitochondrial disease and occur when one of the four respiratory chain complexes become impaired. RCDs are considered to be one of the most common

In addition to energy production, mitochondria play a role in several other cellular activities such as regulating apoptosis which is the programmed self-destruction process of cells and producing substances such as heme which is a component of hemoglobin, and cholesterol (2).

Cells are some of the smallest organisms around. All living things consist of cells, and yet they are invisible to the naked eye. Cells are the basic structural and functional units of life. Cells are made up of many different parts which allow them to function properly.