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irina [24]
3 years ago
6

The diagram shows the structure of starch, a complex carbohydrate. What best describes the relationship between starch and gluco

se?
Biology
1 answer:
serious [3.7K]3 years ago
5 0

Answer:

Glucose is monomer of starch

Explanation:

Starch is polysacheride and glucous is monosaccharide glucose molecules link with glycosidic bond to form starch so c is your answer

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"A microbiology technologist is reading an anaerobic culture and observes a double zone of hemolysis on an anaerobically incubat
mariarad [96]

Answer:

<em>Clostridium perfringens</em>

Explanation:

<em>Clostridium perfringens</em> is a bacterium characterized by being a large, gram-positive, boxcar-shaped bacillus.

It is part of the facultative aerobic bacteria group (they can survive both in the presence or absence of oxygen) and is also a spore-forming bacterium (spores are small structures capable of generating new bacteria).

<em>Clostridium perfringens</em> can cause food poisoning, which results from the ingestion of contaminated food (usually meat and animal products) by the bacteria.

Once in the small intestine, the bacteria releases the toxin that usually causes diarrhea.

4 0
4 years ago
Which of the following statements about energy in systems are true?
12345 [234]

Answer:

Energy can be changed from one form to another

Explanation:

Energy can't be destroyed or created

4 0
2 years ago
Read 2 more answers
What is the difference between chromatids and chromatin?
Ivanshal [37]
Chromatin is the mass of DNA molecules which is undistinguishable however chromatids are part of a chromosome attached with a centromere. Also, chromatin is the DNA before it coils and chromatid are the things that contains the DNA.
6 0
3 years ago
Familial hypercholesterolemia (FH) is an inherited trait in humans that results in higher than normal serum cholesterol levels (
valentinak56 [21]

Answer:

Thanks for you question. Your hypothesis suggests a linear relationship between serum Cholesterol levels and MI. This hypothesis seems to ignore the difference in the prevalence and effectiveness of LDL receptors in the FH patient.

FH patients who have inherited the mutation from both parents have very few LDL receptors in their blood and therefore almost no ability to pass the unused Cholesterol through the liver. FH patients who are heterozygous will have more LDL receptors although both will find Cholesterol removal problematic without the addition of a PCSK9 inhibitor.

In short, your hypothesis need to account for other factors that are in play.

Explanation:

Consider my case. I am a 64 year old male who has Heterozygous Familial Hypercholesterolemia. Before treatment at age 12 my Total cholesterol was 510 mg/dl. My genetic testing shows two mutations to the LDL Receptor gene with only one mutation being pathogenic. My first heart attack was at 47 and first stroke at 62. My current LDL is too low to detect with the use of a PCSK9 inhibitor (Repatha®).

8 0
3 years ago
How many kilometers has each ocean basin has opened in the past 2 million years?
Lena [83]
1.5billion I don't know don't be so harsh?

3 0
4 years ago
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