Step 1: Understanding bacterial superantigens.
Superantigens are a class of bacterial proteins that can activate T cells without the need for antigen processing. They bind directly to T cell receptors (TCRs) and MHC class II molecules, leading to massive T cell activation.
Step 2: Analyzing the options.
(A) bind to VβCDR2 loop in T cells without being processed into peptides: This is correct. Superantigens bind to the Vβ domain of the TCR without requiring processing into peptides.
(B) bind to VβCDR2 loop in T cells after being processed into peptides: This is incorrect. Superantigens do not require peptide processing; they bind directly to the TCR.
(C) are recognized by B cells after being processed into peptides: This is incorrect. Superantigens primarily affect T cells, not B cells.
(D) bind to VβCDR1 and HV4 loops in T cells without being processed into peptides: This is incorrect. Superantigens typically bind to the VβCDR2 region of TCR, not VβCDR1 and HV4 loops.
Step 3: Conclusion.
The correct answer is (A) bind to VβCDR2 loop in T cells without being processed into peptides, as bacterial superantigens directly interact with the Vβ region of the TCR.
In the following figure, the radius of the circle circumscribing the regular hexagon is 2 cm. The area of the shaded region is ............ cm\(^2\) (round off to 2 decimal places) 
Which of the following statements is/are TRUE for the function \( f(x) \) shown in the figure given below? 
In an experiment to examine the role of exopolymetric substances (EPS) on bacterial growth, a wild-type strain (S⁺) and a mutant strain deficient in EPS production (S⁻) were grown in monocultures as well as in co-culture (in equal proportion of S⁺ and S⁻). The CFU (colony forming units) of these cultures measured after 24 hours are shown in the following figure. 
Which one of the following phenomena best describes the interaction between the wild-type strain (S⁺) and mutant strain (S⁻)?
Match the diseases in Group A with their corresponding causative microorganisms in Group B 
Match the metabolic pathways in Group A with corresponding enzymes in Group B 