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Impact of microbes on human
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THE EFFECT MOIST VS DRY FOOD HAS ON THE AMOUNT OF BACTERIA PICKED UP OFF OF FALLEN FOOD
Lindsey Alexander, Gabby Wnek, Raquel Montoya, and Lauren Burkhart
Introduction
Micro-organisms play a huge part in a human’s life. Microbes are given a bad reputation because they are often known for causing disease, but that is not always the case. Microbes are found on the surface of our skin, in our intestines, and everywhere else. In fact, humans need microbes to survive. Microbes make up more than 60% of the living matter in the world. To put that into perspective, a million microbes could be found in only a teaspoon of soil (“About Microbiology” n.d.).
There are six different kinds of microbes: bacteria, fungi, viruses, protozoa, algae, and archaea.
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Before beginning the dropping trials, one piece of bread was swabbed with a sterile swab and then transferred to a media plate, and then the same process was followed for a slice of banana. One floor tile was then disinfected using CDC-10 disinfectant. Apply S. Marcescens bacteria were applied using a sterile swab in middle of the floor tile. The first piece of banana was then touched to the bacteria infected floor for one second. The banana was then swabbed on the side that became exposed to the bacteria and then was swabbed onto the media plate. The same floor tile was then disinfected and the bacteria were reapplied. Then, the same process was completed using a piece of bread, completing trial one. The experiment then went through two more trials completing the previous steps with a new piece of banana and bread each time, disinfecting the floor tile in …show more content…
The data was then recorded into a data table, and the average amount of bacteria for banana and bread were calculated by averaging the three trials. This completed our experiment.
Results
Before dropping the banana and bread onto the floor we recorded the amount of bacteria on fresh banana and bread, results are recorded in Table 1. In the first trial of the experiment the banana and the bread was dropped for five seconds before swabbing for the amount of bacteria that was picked up. After 48 hours of storing the plates at room temperature, the first two trials of dropping the banana on the bacteria contained too many bacteria colonies to count (Figure 1). We decided the bacteria had to many to count because the whole plate was covered with bacteria. Even though we could count the number of colonies for the third trial of the banana, 148 colonies, the average of colonies that were on the banana for all three trails was too many to count (Table 1). The colonies of the bread that were on the plates are recorded in Table 1. The average of the colonies that were counted for the bread was 153 colonies (Table
I identified the genus and species of an unknown bacterial culture, #16, and I applied the following knowledge of morphologic, cultural and metabolic characteristics of the unknown microorganism according to the laboratory manual as well as my class notes and power point print outs. I was given an incubated agar slant labeled #16 and a rack of different tests to either examine or perform myself; the tests are as follows: Gram Stain; Nutrient Gelatin Test; Carbohydrate Fermentation; Dextrose, Lactose and Sucrose; IMVIC tests; Citrate, Indole, Mythel-Red and Vogues Proskauer test; as well as a Urease and TSI Test.
The first day an unknown sample was assigned to each group of students. The first test applied was a gram stain to test for gram positive or gram-negative bacteria. The morphology of the two types of bacteria was viewed under the microscope and recorded. Then the sample was put on agar plates using the quadrant streak method for isolation. There were three agar plates; one was incubated at room temperature, the second at 30 degrees Celsius, and the third at 37 degrees Celsius. By placing each plate at a different temperature optimal growth temperature can be predicted for both species of bacteria.
In this lab project, the microbiology students were given 2 unknown bacteria in a mixed broth each broth being numbered. The goal of this project is to determine the species of bacteria in the broth. They had to separate and isolate the bacteria from the mixed broth and ran numerous tests to identify the unknown bacteria. The significance of identifying an unknown bacteria is in a clinical setting. Determining the exact bacteria in order to prescribe the right treatment for the patient. This project is significant for a microbiology students because it gives necessary skills to them for future careers relating to clinical and research work.
After the end of the experiment the unknown 10 sample was Staphylococcus epidermidis. Came to this conclusion by first beginning with a Gram Stain test. By doing this test it would be easier to determine which route to take on the man made flow chart. Gram positive and gram negative bacteria have a set of different tests to help determine the unknown bacterium. Based on the different tests that were conducted in lab during the semester it was determined that the blood agar, MSA, and catalase test are used for gram positive bacteria while Macconkey, EMB, TSI, and citrate tests are used for gram negative bacteria. The results of the gram stain test were cocci and purple. This indicated that the unknown bacteria were gram positive. The gram stain test eliminated Escherichia coli, Klebsiella pneumonia, Salmonella enterica, and Yersinia enterocolitica as choices because these bacteria are gram negative. Next a Blood Agar plate was used because in order to do a MSA or a Catalase test there needs to be a colony of the bacteria. The result of the Blood Agar plate was nonhemolytic. This indicated that there was no lysis of red blood cells. By looking at the plate there was no change in the medium. Next an MSA test was done and the results showed that there was growth but no color change. This illustrates that the unkown bacteria could tolerate high salt concentration but not ferment mannitol. The MSA plate eliminated Streptococcus pneumonia and Streptococcus pyogenes as choices since the bacteria can’t grow in high salt concentration. Staphylococcus aureus could be eliminated because not only did the unknown bacteria grow but also it didn’t change color to yellow. Lastly a Catalase test was done by taking a colony from the Blood Agar plate...
Jennifer Ackerman's main focus in her article The Ultimate Social Network, is that of the functions concerning bacteria within humans. Although scientists have had presumptions about humans being proficient in governing their body’s innermost structure, they soon come to recognize the sophistication of our inner space which holds an extensive plethora of bacteria and other microorganisms that lie within each and every one of us. Moreover, scientists' new and emerging view of how the human body operates, and the cause of increasing present-day diseases (i.e. obesity and different autoimmune disorders) are uncovered by analyzing effects of certain microbe species in our bodies. By italicizing on points such as the above, in conjunction with bacteria's genetic variations, and modern computing technology, the author proves that scientists are quickly progressing with the characterization the most prevalent species of microbes, which, in her opinion, is definitely paying off.
The eighteenth exercise of the laboratory manual titled Unknown Identification and Bergey’s Manual is an experiment to identify an unknown bacterium. In this exercise, a student must randomly choose a numbered bacterium available to the class. The keys in Appendix H, located on the last pages of the book, are the major helpful tools in this exercise because it provides completed steps of tests that needs to be performed in order to distinguish certain bacteria. This means that in this exercise, various types of tests and techniques must be performed to identify the chosen unknown bacterium. The unknown bacterium that I selected was number thirty-nine in which I discovered as the Bacillus megaterium after conducting several tests.
Bacteria play a large role in our health, the environment, and most aspects of life. They can be used in beneficial ways, such as decomposing wastes, enhancing fertilizer for crops, and breaking down of substances that our bodies cannot. However, many bacteria can also be very harmful by causing disease. Understanding how to identify bacteria has numerous applications and is incredibly important for anyone planning to enter the medical field or begin a career in research. Having the background knowledge of identifying an unknown bacteria may one day aid healthcare professionals diagnose their patient with a particular bacterial infection or help researchers determine various clinical, agricultural, and numerous other uses for bacteria.
During her presentation, Bonnie Bassler expends many different aspects of communication in a bacterial level and how successful communication is important to survival and efficient functioning. It is evident from her presentation that without a common language to communicate with, bacteria could not work as efficiently as they do, neither to immunize people nor create havoc in them. In her presentation, Bassler asserts the importance of the use of language in communication in bacteria, using rhetorical appeals – logical, ethical and emotional – and how it is consequently related to humans.
Inconsistencies in this lab could have caused variations in data collecting. Collecting data from one petri dish was challenging because something could have been different on other petri dishes if this experiment was tested on several petri dishes. This could have been different because the other petri dishes could have had more micro-organisms in Section 2 instead of Section 1, or no bacteria could have grown at all in every section of the petri dish.- Second, nothing grew in section B even though there were no disinfectants in that section. The reason why the bacteria and mold might have grown in sections 1, 2, and 3 was because in the process of making the experiment, the coffee filter papers were touched with glove free hands and were not clean. If this lab was run again, some changes would be to wear rubber gloves, do not pour the hand sanitizers on the coffee filter paper but just pour one pump straight into the petri dish, have more than one petri dish to collect data off of, and check when the last time someone cleaned the door knob
In short, the book 'Deadly Companions: How Microbes Shaped Our History' explains the dynamism, the changing interactions between humans and microbes, and the way and extent to which these interactions have influenced the human cultural history. This book is very useful because it tell us that we must strive to understand what makes microbes successful as we are faced with unrelenting microbial drug resistance. Microbes mutate to fatal human pandemics and it’s for this reason that we need to adopt a microbe centric world views.
...standing the nature of relationship between the residing microbes inside human cells and about their function is very important to put an end to this war and to live in peace with the natural organisms that are benefitting human body and their survival has become our primary importance.
Gut micorbiota has been a large-scale research in recent years. It is shown that the gut microbiota coevolves with us (Ley et al, 2008). Over 100 trillion of gut microbiota are produce by the body which have an large impact on the immune system, human physiology, metabolism and nutrition (Ley et al, 2006). Disablility of the gut to harbour the community of microbial cells has been linked to gut diseases, such as inflammatory bowel disease (IBD), encompasing ulcerative colitis, Crohn's disease, diabetes, obesity (Zhang et al, 2009) and malnutrition (Kau et al, 2011). It is also known as the hidden metabolic 'organ'. The gut produces a variety and complex microbial community which acts an important role in human health. It has been estimated that 1000 bacterial species and 100-fold genes can be found in human gut (Ley et al, 2006). The newborn's digestive tract was sterile, gut microbiota starts to colonised rapidly after birth and continue its evolution throughout life. Enterobacter, Enterococci, Bifidobacteria, Clostridia, Streptococci are the early colonizers. The composition of gut microbiota is unique in each individual, with a small phylogenetic overlap between people. Even in twins they share less than 50% of species phelotype (Turnbaugh et al, 2010). It is shown that there is a stable core microbial colonies in an individual even though it can be influences by aging, diet, environment and health status (Qin et al, 2010).
There were five test solutions used in this experiment, water being the control, which were mixed with a yeast solution to cause fermentation. A 1ml pipetman was used to measure 1 ml of each of the test solutions and placed them in separated test tubes. The 1 ml pipetman was then used to take 1ml of the yeast solution, and placed 1ml of yeast into the five test tubes all containing 1 ml of the test solutions. A 1ml graduated pipette was placed separately in each of the test tubes and extracted 1ml of the solutions into it. Once the mixture was in the pipette, someone from the group placed a piece of parafilm securely on the open end of the pipette and upon completion removed the top part of the graduated pipette.
Microbes are microscopic life forms, usually too small to be seen by the naked eye. Although many microbes are single-celled, there are also numerous multi-cellular organisms. The human body has 10-100 trillion microbes living on it, making it one giant super-organism. Since the first link between microbes and diseases was made, people have been advised to wash their hands. Scientists, however, have recently started to investigate more closely how the microbes that call the human body home affect our health. While some microbes cause disease, others are more beneficial, working with our bodies in many subtle ways.
Food-borne illnesses fall into two categories, intoxicant and infections. An understanding of the causes and preventions will limit any contaminations. The food preparation process emcompresses the sanitation process from