Krebs Cycle 101 - Understanding The CC Formula

The Krebs Cycle

The Krebs cycle is the process cells use to convert nutrients into energy—the cycle named after Hans Krebs, the German scientist who described it in 1937. The Krebs cycle is called the citric acid or tricarboxylic acid (TCA cycle). The Krebs cycle occurs in the mitochondria, which are the parts of cells that convert food into energy.

The cycle starts when glucose and oxygen molecules are combined to form a molecule of carbon dioxide and water. This reaction releases energy, which the cell can use to make ATP, the energy-carrying molecule that cells need to do their work.

Oxidative phosphorylation occurs in the mitochondria and produces ATP by transferring electrons from glucose and oxygen to carbon dioxide and water molecules. The utilization of these electrons results in the production of ATP.

The protection provided by at least 32 steps in the process provides a system that protects oxygen-driven plants and animals. In the Krebs cycle, these steps control how fast electrons transfer from one molecule to another. It contains the rate of ATP production and prevents the buildup of harmful toxins in cells. The cycle starts with a molecule of glucose, which breaks down into two pyruvate molecules. Pyruvate then converts into acetyl-CoA, which enters the Krebs cycle.

In the Krebs cycle, acetyl-CoA is combined with a four-carbon molecule called oxaloacetate to form a six-carbon molecule called citrate. The breakdown of citrate occurs, leading to the formation of a five-carbon molecule known as alpha-ketoglutarate. Subsequently, alpha-ketoglutarate breaks down into a four-carbon molecule called succinate.
The process further converts succinate into a four-carbon molecule known as fumarate. Following this, fumarate transforms a five-carbon molecule called malate. Malate is then converted back into oxaloacetate, thus initiating the cycle once more.

The Krebs cycle is vital because it produces ATP, the energy-carrying molecule cells need to do their work. The process also produces carbon dioxide, released from cells and used by plants for photosynthesis.

Cell Cycle and Cancer

Lower-order organisms are less complex in their metabolic pathway than higher-order organisms, such as trees or humans. The cycle followed by organisms such as bacteria and fungi, as well as specific diseased cells in higher-order life forms, tracks a less complicated process that allows the disease to multiply almost exponentially in an anaerobic cycle with far fewer steps.

Warburg first observed the unique metabolic cycle of cancer cells and their ravenous appetite. The disease utilizes all available minerals, sugars, fats, and proteins to fuel the reproduction of cells using the abbreviated anaerobic cycle.

An elevated replication rate decreases oxygen availability for the healthy tissues surrounding the disease. These reduced oxygen levels promote fermentation, a crucial component of the favorable conditions necessary for the rapid proliferation of cells and organisms using the anaerobic cycle, which includes infections and abnormal cells.

The CC Formula exploits a flaw in the exponential expansion mechanism of the disease organism.

Specifically, it exploits the mineral-gathering mechanism of the organism against itself. Lower orders of disease organisms gather the necessary minerals and other building blocks in an amount proportional to their availability in the environment. It differs from the metabolic processes of higher organisms, whichTherefore, providing a high concentration of ionic minerals to a disease area could result in a toxic level of the mineral to disease organisms and allow survival of higher organisms, so long as the dosage rate of the ionic minerals is below the unhealthy level for the higher organism.
The CC Formula uses highly bio-available ionic minerals at a rate that will kill the lower organism without impairing the function of the higher organism. This formulation transports all the minerals systemically to a plant, animal, or human with the assistance of an artificial superoxide dismutase (SOD) carrier.
The artificial SOD carrier causes the disease-causing cell or organism to uptake an amount of toxic ionic mineral, which results in the death of the diseased cell or organism. Moreover, many diseases undergo anaerobic fermentation, impairs oxygen, indicating a secondary mechanism for combating the infection. The CC Formula also contains sulfur, which may destroy illness and relieve pain. only gather enough of the elements and building blocks to satisfy the requirements of the Krebs cycle.

Higher organisms will only incorporate minerals and other nutrients at a rate necessary for survival, while lower organisms and certain diseased cells will accumulate minerals in an amount that is toxic.

Therefore, providing a high concentration of ionic minerals to a disease area could result in a toxic level of the mineral to disease organisms and allow survival of higher organisms, so long as the dosage rate of the ionic minerals is below the toxic level for the higher organism.

The CC Formula uses highly bio-available ionic minerals at a rate that will kill the lower organism without impairing the function of the higher organism. This formulation transports all the minerals systemically to a plant, animal, or human with the assistance of an artificial superoxide dismutase (SOD) carrier.

The artificial SOD carrier causes the disease-causing cell or organism to uptake an amount of ionic mineral that is toxic, which results in the death of the disease cell or organism. Additionally, many diseases follow an anaerobic fermentation process in which oxygen will impair, thereby suggesting a secondary mechanism for destroying the disease. The CC Formula also contains sulfur, which may further aid in destroying disease and relieving pain.

However, the prime mode of action is the uptake of minerals in a highly biologically available formulation.

The general principle of the CC Formula is the rapid entry into the aerobic biological system of a plant or animal using a mineral complex carrier in an ionic form that penetrates and migrates toward an anaerobic disease system if present. The product can penetrate the barrier zone between the aerobic and anaerobic tissues if the disease is internal.

Other mineral formulations are less bioavailable and unable to pass through cellular tissues as quickly as the CC Formula. The unique quality of the formulation is thus its penetration of the membrane and the movement of large amounts of ionic minerals into the disease area.

Diseases have three vulnerable sites that can be attacked by treatment:

1. Penetrating the outer membrane of the disease.
2. Destroying the internal components that drive the metabolism of the cells.
3. Destroying the gene pool that may provide a future defense (resistance) against the introduced substance.
Minerals not in the bioavailable form will not be able to eliminate or otherwise disable the disease cells because the minerals cannot pass through the membrane coating the outer surface of the disease cells or cannot travel in an extracellular fashion. The bioavailable minerals will attack all the vulnerable targets in the disease cells because of the systemic capabilities of the formulation.
When using the bioavailable formulation, the cell membrane should be easily transversed and possibly ruptured, the inner cell compromised because of the Krebs cycle (aerobic vs anaerobic) as described above, and the genetic code of the disease cell destroyed by apoptosis. There should be no further deviations from the genetic code to produce new strains that may be resistant to the CC Formula. There are no known resistances to plant or animal disease when the primary source of the product used is a mineral.

Discover The Research Behind The CC Formula