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tatyana61 [14]
3 years ago
11

Starch can be broken down into the disaccharide known as _____. starch can be broken down into the disaccharide known as _____.

lactose glucose sucrose fructose maltose
Biology
1 answer:
Gnom [1K]3 years ago
5 0
Lipids, glucose..................
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What would happen to a food web if we remove the:
salantis [7]
C) Primary Producer. The producers are what make the food chain. Without them there would be no primary consumers. And without primary consumers there would be no secondary consumers.
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3 years ago
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Why does alpha Centauri appear to be yellow-white?
motikmotik

Answer:

It is due to the temperature of the star

Explanation:

The colour of star depends on the temperature of star.

8 0
3 years ago
The pedigree below tracks the presence of dimples through a family's generation. Having dimples is an autosomal dominant trait.
yulyashka [42]

A pedigree is a representation of a family history tracking a trait. The graph shows the inheritance pattern of the trait and its expression through several generations.

<h3>What is an autosomal dominant trait?</h3>

The autosomal dominant trait is the characteristic that is coded by a gene located in an autosomal chromosome (this is, not a sexual chromosome).

This trait is dominant because it is coded by the dominant allele, meaning that the recessive allele codes for the absence of dimples. The presence of only one dominant allele in the genotype is enough for the idividual to express dimples.

<u>               Genotype                                  Phenotype     </u>

DD, Homozygous dominant                        Dimples

Dd, Heterozygous                                        Dimples

dd, Homozygous recessive                       No Dimples

<h3>What is a pedigree?</h3>

The pedigree is the representation of a family history conserning a certain trait. In this case, dimples.

The pedigree shows the expression -and inheritance pattern- of the trait through several generations.

To correctly interpret a pedigree, we need to know that

  • Family members

→ Individuals are represented with geometrical figures.

→ Males are squares

→ Females are circles

  • Trait/Phenotype

→ Healthy/normal/not affected  individuals are represented with empty figures

→ Affected/mutated individuals are represented with solid black figures

  • Generations

→ Each file is represented with a roman number, indicating the Generation.

Here we will assume that

  • Individuals represented with solid figures express dimples -shaded individuals-. They can be either DD or Dd. This is because dimples is not usuall.
  • Individuals with no dimples are represented with empty figures and are dd.

According to the provided pedigree,

I-1 ⇒ man DD or Dd

I-2 ⇒ woman dd

II-1 ⇒ man Dd or DD

II-2 ⇒ woman dd

II - 5 ⇒ woman dd

III - 1 ⇒ man Dd

III- 2 ⇒ woman dd

III - 6 ⇒ woman dd

Since this pedigree does not specify the relationship between individuals, I can not answer the question based on it. So, I will attach another tree to specify genotypes.

I advise you study this new example, and then follow the same reasoning to choose the correct individual according to you pedigree.

Yo can learn more about pedigrees at

brainly.com/question/19516649

#SPJ1

7 0
1 year ago
Are mutations always deleterious?
insens350 [35]
Most are but not always
6 0
2 years ago
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A young animal has never had much energy. He is brought to a veterinarian for help and is sent to the animal hospital for some t
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Answer:

A. His mitochondria lack the transport protein that moves pyruvate across the outer mitochondrial membrane.

Explanation:

Pyruvate is from the breakdown of carbohydrates such as glucose through glycolysis. Glucose enters the cytosol through specific transporters (the GLUT family) and is processed by one of several pathways depending on cellular requirements. Glycolysis occurs in the cytosol and produces a limited amount of ATP, but the end product is two 3-carbon molecules of pyruvate, which maybe diverted again into many pathways depending on the requirements of the cell. In aerobic conditions, pyruvate is primarily transported into the mitochondrial matrix and converted to acetyl-coenzyme A (acetyl-CoA) and carbon dioxide by the pyruvate dehydrogenase complex (PDC).

Initially it was proposed that pyruvate was able to cross the membrane in its undissociated (acid) form but evaluation of its biochemical properties show that it is largely in its ionic form within the cell and should therefore require a transporter.

Transport of pyruvate across the outer mitochondrial membrane appears to be easily accomplished via large non-selective channels such as voltage-dependent anion channels/porin, which enable passive diffusion. Indeed, deficiencies in these channels have been suggested to block pyruvate metabolism

7 0
3 years ago
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