plant extract made with distilled water. P.aeruginosa gave a maximum zone size of 20mm in diameter at 80% concentration of plant extract with ethanol. Klebsiella spp gave a zone size ranging from 4-9mm with different concentrations of plant extract with ethanol‚ 3-10mm with acetone and 2-8mm with plant extract made with distilled water. Klebsiella spp gave a maximum zone size of 10mm in diameter at 80% concentration of plant extract with acetone. (Table
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INTRODUCTION As for the visual documentation of a living or dead specimen‚ digital photography has largely replaced traditional illustrations of the living specimen as the standard method of recording the colour and anatomy of the specimen in the field today. Earlier traditional illustration (coloured and black and white) are still considered scientifically important because they can stress fine anatomical features that are often obscured by liquid. Even today‚ these earlier traditional illustrations
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Specific enzymes lower the activation energy for specific reactions and shapes. Activation energy is required to start a chemical reaction. This occurs when energy is added to reactants. Amino acid chains are made up by their unique folds which results in formation. Since enzymes are proteins‚ each one consists of its own amino acid in a specific order. Since hydrogen bonds are weak‚ they form between amino
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human evolution. Although no humans are being observed in this lab the concept of evolution is going to be looked up. The speciation is to see if by different modifications in the environment create a new species of finches. If no new species develop or the finches do not evolve to the changes in their surroundings will natural selection happen and will we no longer have finches on this island? Materials * Computer * Evolution Lab * Internet Methods or Procedures (All changes are done
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two lights (2 light bulbs) and the fourth contained three lights (3 bulbs). There was no fifth station because our test tube number two was kept in the dark. We then measured the transmittance in four runs‚ using the spectrometer and recorded our results (Figure
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Data Analysis: 1. What was the temperature change for the water in the calorimeter (ΔTwater)? 3°C 2. What was the temperature change for the metal sample (ΔTmetal)? Assume the intial temperature of the metal was the same as the temperature of the water it was boiled in. 70°C 3. What was the specific heat of water in J/g°C? 4.186 J/g°C 4. Using the following equation‚ your answers to questions 1-3‚ and your data table‚ determine the specific heat of the metal sample you tested. 5
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Introduction The purpose of this lab is to understand how each offspring inherits its genotype and how its phenotype reflects it. Sex chromosomes determine the sex of the offspring‚ and the autosomes consist of all the other chromosomes that determine phenotypic traits. Dominant traits are the genes that are expressed‚ while the recessive traits are masked by the dominant traits. We used Drosophila melanogaster (fruit fly)‚ mutating the female fruit fly with a scalloped gene to change the phenotype
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Abstract: In this Lab we used the chemical DPIP to detect the rate of succinate broken down by the mitochondrial solution. We detected the amount of DPIP in the solution with a spectrophotometer and measuring the absorbance of light at the 600nm range. DPIP is a useful chemical to use in this experiment because it goes from a blue color when oxidized to a colorless liquid (Ogura‚ 281)‚ this is due to the hydrogen ions and electrons released during the transitional step between succinate and fumarate
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animal though? In this experiment we are using lab mice‚ Mus musculus‚ to see if the introduction of a predator scent (fox urine) increases‚ decreases‚ or has no effect on the metabolic rate within them. We will calculate the mass specific metabolic rate and use a t-test to determine if there is a significant change in metabolic rate when the mouse is exposed to the predator urine and when it is not exposed. With these mice being born and raised in a lab‚ the fox urine should have no effect on the metabolic
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Halobacterium Lab Investigation Mason Pirio 12/12/13 Period 5 Table Group 3 PS 2- Experiment Design PS 3- Conclusion Writing PS 13- Nitrogen Cycle Abstract- In this experiment we tested to see how well halobacterium grows in different levels of salinity. We found out that the higher salinity in the growth medium the better the halobacterium grows. Background Information- Halobacterium is a bacteria that is found in the great salt lake. Halobacterium is an extremeophile which means it thrives
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