Evidence for evolution, in other words evidence of common descent, include fossils, which have shown a (fairly) steady change in morphology over time for some species. An example would be horse hooves: we have fossils that show when they were still three toed, then two toed, then one toe in our present day horses. Another piece of evidence is vestigial organs. An example of vestigial organs is wings in some flightless birds, such as the kiwi. Their ancestors used it in order to fly across the marine barrier into New Zealand, but natural selection and random genetic drift made them quickly lose the ability to fly. Nonetheless, they still have their wings, however small. It can be assumed that eventually, their wings would be reduced to small stubs fused to other nearby bones, as has been observed in their cousins.
If you want to grow up a large quantity of streptomycin-resistant E. coli, you would require to pick a colony of the bacteria from the streptomycin-positive plate and allow to grow it on a streptomycin positive plate.
<h3>What is E. coli?</h3>
E. coli may be defined as a type of bacterium that is commonly present in the intestinal regions of humans and other animals, some strains of this bacterium can significantly cause severe food poisoning.
The strain of streptomycin-positive is those population of E. Coli which is significantly streptomycin resistant, while the negative strain has the opposite effect.
That's why if you want to grow up a large quantity of streptomycin-resistant, you must remarkably require to pick only a positive strain of streptomycin for E.Coli bacterium.
Therefore, if you want to grow up a large quantity of streptomycin-resistant E. coli, you would require to pick a colony of the bacteria from the streptomycin-positive plate and allow to grow it on a streptomycin-positive plate.
To learn more about E. Coli, refer to the link:
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Most of all cell enzymes are proteins
Answer:
Gap 2 (G2): During the gap between DNA synthesis and mitosis, the cell will continue to grow and produce new proteins. At the end of this gap is another control checkpoint (G2 Checkpoint) to determine if the cell can now proceed to enter M (mitosis) and divide.
Explanation:
