That simply means this:
That the enzymes natural reaction to the concentration of the of the substrate (based on its chemical makeup) will react at .4 slygometers. This is based on the Scale of Enzyme dependency on the substrates, again "natural" reaction to the enzymes reaction on itself. Never let it fool you that 1/8th of a slygometer is equivalent to a Decominuter on the Enzyme Friction Scale. This is a common misconception and more so just a blatant misunderstanding of the rudimentary basis of the scale itself.
For those of you who don't know the scale conversions they are as follow:
Slygometer Ct. Decominuter Value
.4 .114
.8 .228 * and so on.
Also please wear gloves when marrying any of these chemicals if the Decominuter reads above .14. The reason is, is that the chemical begins to decompose and speed up the half life of itself based on the Degeneration theory, this can cause a devastatingly harsh burn on your knuckle or finger pad. Believe me it hurts bad, there is a procedure to stop the burn from sinking to the bone called Micro-Magnesis, highly expensive if your lucky enough to bump into the Doctor Who holds qualification to do so.
The molecule upon which an enzyme acts is called the substrate.
To find out how enzyme concentration affects the activity of the enzyme you must:vary the concentration of the enzyme, by preparing different concentrations (keeping the volume of solution the same)keep the temperature, substrate concentration and pH constantmeasure the activity of the enzyme at each concentrationHow the enzyme activity is measured will depend on the specific enzyme involved.You need to have plenty of substrate (excess substrate) so it doesn't run out during the experiment.In this type of experiment, the enzyme activity is the dependent variable, the temperature, pH and substrate concentration are control variables and the enzyme concentration is the independent variable.
Depends on how much substrate the enzyme can process. Most enzymes can process more than one molecule of substrate without denaturing or becoming unusable. However, in the terms of your question. More substrate is better. Too many enzymes would mean the reaction would be cut short, because they would all react the substrate at once. So for a prolonged, efficient reaction more substrate would be proper.
An enzyme will alter its substrate although the specific substrate depends on the enzyme.
The enzyme activity depends on the conditions of the reaction and the enzmye used. The term enzyme activity refers to the rate at which substrate is converted into product and can be measured in many different ways.
The molecule upon which an enzyme acts is called the substrate.
To find out how enzyme concentration affects the activity of the enzyme you must:vary the concentration of the enzyme, by preparing different concentrations (keeping the volume of solution the same)keep the temperature, substrate concentration and pH constantmeasure the activity of the enzyme at each concentrationHow the enzyme activity is measured will depend on the specific enzyme involved.You need to have plenty of substrate (excess substrate) so it doesn't run out during the experiment.In this type of experiment, the enzyme activity is the dependent variable, the temperature, pH and substrate concentration are control variables and the enzyme concentration is the independent variable.
Depends on how much substrate the enzyme can process. Most enzymes can process more than one molecule of substrate without denaturing or becoming unusable. However, in the terms of your question. More substrate is better. Too many enzymes would mean the reaction would be cut short, because they would all react the substrate at once. So for a prolonged, efficient reaction more substrate would be proper.
An enzyme will alter its substrate although the specific substrate depends on the enzyme.
It depends on what type of isomerization is occurring; configurational or stereoisomerization. Use of equilibrium concentrations and/or catalysis concentration strategies would work.
The number of moles of catalyst depends on the reaction under consideration. Compared to the substrate, about 10-2 to 10-6 times of the catalyst can be used. The lower the amount of the catalyst, the more effective it is.
The enzyme activity depends on the conditions of the reaction and the enzmye used. The term enzyme activity refers to the rate at which substrate is converted into product and can be measured in many different ways.
There is none, glass is much stronger, but i suppose it depends on the use.
It basically depends on the biasing of a transistor. In case of a MOSFET, it depends on the substrate biasing.
Enzymes act on molecules called substrates. The kind of substrate depends on the shape of the enzyme.
it will control the flow of electrons between the source and drain,the controlling will be depends upon the input voltage to the substrate.
Without knowing the enzyme you are interested in, it is hard to give an exact answer. It all depends on the amount of the substrate, temperature, the resultant product, whether either is involved in a chain reaction or a simple reaction and if there is a co-enzyme involved. See the link below for more information on the reaction: