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Anna [14]
3 years ago
7

Fill in the blanks

Biology
2 answers:
pickupchik [31]3 years ago
5 0

Answer:

1.Sunlight.

2.The sun.

<h2>Hope it helps you .</h2><h2>:-)</h2>
harina [27]3 years ago
3 0

Answer:

Solar energy/Radient energy is used by plants to prepare their foods.

Solar energy is the main source of energy for the earth.

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Central vacuole...storage is the correct answer

Explanation:

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Why does a protein not function after it has been denatured?
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Answer:

d. The normal bonding between the R groups has been disturbed and the protein loses its normal shape.

Explanation:

Denaturation is the loss of function of a protein due to its altered three-dimensional structure. To function properly, proteins must be present in a properly folded form. The three-dimensional structure and protein folding are mediated by weak interactions such as hydrogen bonds, electrostatic interactions, etc. An abrupt increase in temperature, pH or presence of some organic solvents causes protein denaturation.

The organic solvents target the hydrophobic interactions between the R groups of amino acids that make the core of globular protein stable. Extreme levels of pH target the net charge on proteins and thereby results in electrostatic repulsion between closely placed amino acids. Extremes of pH also disrupt the hydrogen bonding between the R groups of the amino acids. The effect is the loss of the three-dimensional structure of proteins, their partial or complete unfolding and loss of function.

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3 years ago
You are a graduate student in the lab of a famous fly geneticist. You need to analyze a batch of mutant flies that were recently
bazaltina [42]

Answer:

knirps (a gap gene)

wingless (a segment-polarity gene)

kruppel (a gap gene)

even-skipped ( a pair-rule gene)

hunchback (a gap gene)

hedgehog (a segment-polarity gene)

Explanation:

The gap, segment-polarity and pair-rule genes play central roles in controlling embryonic development of arthropods. In the first place, the gap genes are associated with the formation of contiguous body segments, thereby mutations in these genes result in gaps in the normal body plan of the embryo. For example, in <em>Drosophila melanogaster</em>, mutations in the <em>knirps, Krüppel </em>and<em> hunchback</em> genes result in deletion of body segments. These genes are also known to regulate segment polarity genes, which determine the polarity of the embryonic parasegments by modulating Wnt and Hedgehog signaling pathways. Finally, the pair-rule genes work together with gap genes to control embryonic development of alternating body segments.

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