Alpha-galactosidase catalyzes the hydrolysis of glycolipids and glycoproteins . It is a glycoside hydrolase enzyme that hydrolyzes from its terminal alpha-galactosyl moieties. Insertional inactivation is used to classify the transformed bacterial cells that have taken recombinant plasmids in bacterial DNA technology.
The colonies of recombinant bacteria appear white in contrast to blue colonies of nonrecombinant bacteria because of non-recombinant bacteria containing \(\beta\)-galactosidase.
In cloning experiments, blue-white screening is done to detect recombinant bacteria. α-complementation plays a major role evaluation of the recombinant nature of the bacteria.
Also Read: Bacterial Transformation
Frequency of recombination between gene pairs on same chromosome as a measure of the distance between genes to map their position on chromosome, was used for the first time by
A sphere of radius R is cut from a larger solid sphere of radius 2R as shown in the figure. The ratio of the moment of inertia of the smaller sphere to that of the rest part of the sphere about the Y-axis is : 
AB is a part of an electrical circuit (see figure). The potential difference \(V_A - V_B\), at the instant when current \(i = 2\) A and is increasing at a rate of 1 amp/second is:
Three identical heat conducting rods are connected in series as shown in the figure. The rods on the sides have thermal conductivity 2K while that in the middle has thermal conductivity K. The left end of the combination is maintained at temperature 3T and the right end at T. The rods are thermally insulated from outside. In steady state, temperature at the left junction is \(T_1\) and that at the right junction is \(T_2\). The ratio \(T_1 / T_2\) is 
Recombinant DNA technology is the process used for producing new genetic combinations by joining different genetic material (DNA) together and inserting them into host organisms from two different species or sources. These new combinations are of value to medicine, science, industry, and agriculture.
Step 1- Isolation of Genetic Material.
Step 2- Cutting the gene at the recognition sites.
Step 3- Amplifying the gene copies through Polymerase chain reaction ( PCR)
Step 4- Ligation of DNA Molecules.
Step 5- Insertion of Recombinant DNA into Host.