As we have seen, you can analyze the kinetic properties of a Michaelis enzyme by measuring its velocity of catalysis at a range of substrate concentrations and plotting [S] vs V, or 1/[S] vs 1/V. You can also analyze the properties of an enzyme inhibitor by carrying out the same experiment and graphic analysis in the presence of the inhibitor. If you do this for a noncompetitive inhibitor, what difference will you see when you compare the enzyme kinetics to an uninhibited control

some fungi obtain their nutrients from a living host (plant or animal) and are called most biotrophic fungi have fairly narrow host ranges—they are specialized on a limited called rhizomorphs that allow the fungus to grow from one tree to another. ascospores are formed inside a sac-like structure called an ascus. so your answer is a

measuring light intensity

light meters can be used to measure light intensity. the meter is held at the soil surface and pointed in the direction of the maximum light intensity, and then the meter is read.

errors can be made when measuring light intensity by accidentally shading the light meter. the reliability of the results can be checked by taking many samples.

the principle of segregation describes how pairs of gene variants are separated into reproductive cells. from his data, mendel formulated the principle of segregation. we now know that the segregation of genes occurs during meiosis in eukaryotes, which is a process that produces reproductive cells called gametes.