Question

In: Biology

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. )

Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on the Internet. (Microbial inhibitors are added to prevent growth of microbial contamination of the product AFTER it has been processed.)

a. bottled herb-flavored vinegar

b. bottled herb-flavored oil

c. canned oranges

d. canned sauerkraut

2. People have long known that drinking beer might be safer than drinking water because pathogens can't survive in beer. Which, if any, of the following does NOT prevent the growth of pathogens in beer?

a. ethanol

b. hops

c. yeast

d. a low pH

e. All of the above prevent growth of pathogens in beer.

3. Although Typhoid Mary did not recall ever having typhoid fever, she apparently was infected (possibly sub-clinically) at some point in her life, because she was the source of two epidemics. (It is impossible to transmit the disease if you are never infected!) Which of the following statements regarding Typhoid Mary is NOT correct?

a. She was an incubatory carrier.

b. She was a convalescent carrier.

c. She was an asymptomatic carrier.

d. She was a reservoir host for the bacteria.

e. She was the index case for these outbreaks.

4. All of the following are components of the Gram-negative cell wall EXCEPT:

a. cytoplasmic (plasma) membrane

b. lipid A

c. outer membrane

d. LPS

e. O-antigen

f. All of the above are components of the Gram-negative cell wall

Solutions

Expert Solution

Answer 1- Correct answer is (B) Bottle Herb-Flavored oil

Explanation:-

In Herb-flavoured Oil, Garlic and herbs are placed in oil at oxygen free environment that favours the growth of bacteria (Clostridium botulinium). So a specific level of acidification by microbial inhibitors is required to inhibit the growth of these bacteria.

Answer 2- Correct answer is (C) Yeast

Explanation:-

Pathogens cannot survive in beer, due to the presence of antimicrobial agent’s like hop (hop bitter acid), ethanol, low pH.

Ethanol inhibits cell membrane functions and inactivates bacterial activity. Low pH (3.4-4.8) is another hurdle that prevents the pathogenic activity, in addition low pH displays a synergistic effect with antimicrobial properties of Hop. It was also reported by Simpson and Hammond (1991) that a slight reduction of 0.2 in pH can increase antibacterial activity by 50 %.

Answer 3- Correct answer is (B) She was a convalescent carrier

Explanation:-

Typhoid Mary was not a convalescent carrier, because convalescent carrier are those who are clinically recovered from the infectious disease, but in the case of Typhoid Mary, she was the index case of disease outbreak that remained undisclosed for a longer period of time. During that period, she remained as asymptomatic chronic carrier as well as incubatory carrier and reservoir host of Salmonella Typhi , that unintentionally infected dozens of people.

Answer 4- Correct answer is (F) All of the above are component of the Gram-negative cell wall

Explanation:-

Cell wall of a Gram-negative bacteria is consists of plasma membrane, a gel like matrix in the periplasmic space. Lipid A, as an endotoxin accountable for toxicity of gram negative bacteria. Outer membrane is also present as an single layer of peptidoglycan surrounded by membranous structure. Lipopolysaccharides (LPS) are molecules consists of lipid and polysaccharide composed of O-antigen, present in the outer membrane of Gram-negative bacteria.


Related Solutions

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. ) Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on...
The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations,...
The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations, manufacturers are required to list the amounts of certain nutrients in their foods, such as calories, sugar, fat, and carbohydrates. This nutritional information is displayed on the food’s package. Calories (C) Sugar (S) Fat (F) Carbohydrates (R) 100 12 0.5 25 130 11 1.5 29 100 1 2 20 130 15 2 31 130 13 1.5 29 120 3 0.5 26 100 2 0...
The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug...
The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug should contain less than 25mg of the active ingredient “toxin”, which is assumed to have dangerous side effects. The FDA would like to restrict the error of “approving the drug despite its too high content of toxin” to a maximum risk of 5% (α ≤ 0.05). Let Xi : “ The content of toxin in the i-th pill [in mg].” ∼ N(µ, σ2 )...
A drug company applied for the approval of the Food and Drug Administration (FDA) to market...
A drug company applied for the approval of the Food and Drug Administration (FDA) to market a miracle drug that the company believed could cure some cancers. During the period that the application was under consideration the company's stock rose to $65 per share. The president of the company learned that the FDA application was about to be denied. You are a personal friend of the president, and he told you that he believed that the stock will start trading...
The Food and Drug Administration (FDA) is an agency of the United States Department of Health...
The Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services, one of the United States' federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, prescriptions, and other health-related products. The following are a few examples of the powers the FDA has: • Most federal laws concerning the FDA are part of the Food, Drug, and Cosmetic Act....
Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is...
Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is too easy and, as a result, too many drugs are approved that are later found to be pushed for a more lenient approval process so that pharmaceutical companies can get new drugs approved more easily and quickly. Consider a null hypothesis that a new, unapproved drug is unsafe and an alternative hypothesis that a new, unapproved drug is safe. Differentiate Type 1 and Type...
1. In 1995, the Food and Drug Administration (FDA) published new labeling standards for bottled water....
1. In 1995, the Food and Drug Administration (FDA) published new labeling standards for bottled water. (The full text of the final rule can be found at http://cfr.vlex.com/vid/165-110-bottled-water-19705533.) Prior to that time, bottlers could sell regular tap water under a bottled water label. In fact, the FDA estimated that approximately 25 percent of the supply of bottled water was nothing more than ordinary tap water. (a) Consider how these tougher standards eliminated 25 percent of the supply of bottled water....
It was recently announced that the Food and Drug Administration (FDA) will extend its regulatory authority...
It was recently announced that the Food and Drug Administration (FDA) will extend its regulatory authority to E-cigarettes, tobacco pipes, and cigars. They have proposed a ban of these products to those under 18 (in person and Internet sales), those purchasing these products must show identification, a ban on use in public places, and products must include warning labels. The producers of cigars and e-cigarettes must register with the FDA, provide a detailed accounting of their product ingredients, disclose their...
The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution,...
The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution, Caridex, which disolves cavities. In a study conducted by dental researchers at Northwestern University, 21 of the 35 patients with cavities preffered treatment with Caridex to drilling (Gainesville Sun, Feb. 11, 1988). Find a 90% confidence interval for the true proportion of dental patients who prefer having cavities dissolved with Caridex rather than drilled. (0.46,0.74) (0.44,0.76) (0.39,0.81)
(20pts) The Food and Drug Administration (FDA) has established an upper tolerance of 5 parts per...
(20pts) The Food and Drug Administration (FDA) has established an upper tolerance of 5 parts per billion for the cancer-causing substance nitrosamine in beer. Suppose that Pabst and Miller are identified by the FDA as containing excessive concentrations of nitrosamines and are tested by an independent testing agency with the results shown in the accompanying table (in parts per billion). Also suppose that 36 bottles were randomly selected from each brand.                      Stat.     Pabst    Miller                      --------  -----    ------                      Mean      5.25     5.31                      Std. Dev. 1.20     1.44 Specify the null...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT