Identify the steps of the lytic cycle.
The pieces made in replication are
assembled to complete the new virus
particles.
The new viral nucleic acid and viral
proteins are replicated.
The virus attaches to the host cell.
The original virus releases a protein that
causes the cell wall to burst (lysis), killing
the cell and releasing viruses.
The host's DNA is disassembled and the
virus takes over the call's motoholi

Explanation:

During the lytic cycle, bacteria takes over the cell, reproduces new phages, and destroys the cell. It works in 5 phases

1. The virus or phage attaches itself to the cell

2. The phage enters the cell

3. Biosynthesis- Phage DNA replicates and makes phage proteins

4. New phage cells assemble

5. The cell lyses emerge with a new plague

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.