Answer: Nucleiod, Ribosomes, flagella, fimbriae, plasma membrane
Explanation: A typical bacteria cell possess these structures mentioned above. nucleiod is a chromosome , a nucleic acid which can be DNA or RNA, It is the genetic material of cell which every bacteria cell must have. Flagella ensures swimming movement of all bacterial cell. Ribosome of bacteria cells ensures protein synthesis. Since all bacteria cells meet, plasma membrane is permeability barrier, location of enzyme and transports solutes. Fimbriae enables bacterial cells attachment to surfaces
Sedimentary, because of the glaciers that once covered Indiana they lithified which is a part of the rock cycle in the sedimentary division.
Answer:
Bacteria do not possess the tendency to withdraw sequences of introns from a gene, thus, if the gene for the human growth hormone were transcribed, it would translate into a non-functional protein.
When the expression of a gene takes place in eukaryotes, the budding mRNA comprising introns are removed consequently at the time of post-translational processing to produce mature mRNA. Also, the human growth hormone is produced by the pituitary gland in the form of a pre-hormone comprising a leader peptide of about 20 amino acids in length, which need to get removed post-translationally to produce a mature functional protein.
Bacteria do not possess the biochemical machinery either to effectively withdraw the leader peptide after translation or to splice out the introns. Thus, when an unchanged human growth hormone is cloned, the bacteria cannot produce the functional human growth hormone.
Lipid bilayer model was proposed for its structure but it was modified and new structure is according to fluid mosaic model. Plasma membrane is selectively permible as it selects small molecules like lipid etc (composition is also of lipid and as solubility principle like dissolve like) so large and charged molecules like plasma and ion can't pass through it. Lipid are in form of layer so at the chain when ever other phosphate group attach the place conjugate molecule (phospholipid ) formed
Answer:
A Ligase
B False
C To separate the double‑stranded DNA
Explanation:
The Polymerase Chain Reaction (PCR) is a technique widely used in molecular biology laboratories in order to make millions of copies of a specific sequence of DNA. PCR requires deoxynucleotide triphosphates (dNTPs) to synthesize new copies of the target DNA fragment, a thermostable DNA polymerase that adds nucleotides to new DNA strands, and primers that attach to complementary ends at each DNA strand. PCR has three phases: 1-Denaturation, where the double-stranded DNA molecule is heated to separate it into two single (separated) strands; 2-annealing, where the temperature is lowered in order to allow the primers to attach each DNA strand, and 3- extension, where the temperature is increased (again), and the thermostable DNA polymerase adds the appropriate dNTPs to new DNA strands. In consequence, annealing occurs at the lowest temperature. Moreover, during the denaturation stage, the temperature is increased at 90–95°C in order to denature the DNA strands into single strands.
