A scientific poster describing an experiment investigating the effects of different variables on enzymatic activity, with a voiceover providing further information.
Electrochemical, in-vitro in-vivo study of Co (II)-ofloxacin complexIOSR Journals
Ofloxacin complex has been synthesized and screened for its physicochemical, microbial as well as pharmacological activity have been done in solid and aqueous phase. On the basis of elemental analysis, polarographic studies, amperometric titration and IR spectral studies the probable formula for the complex has been determined at 30±1OC and ionic strength of μ= 1.0[KCl]. Raper’s paper disc method was used for microbial study against various pathogenic bacteria and fungi.Invivo syudy of Swiss mice [25-30gm] were used for antibacterial activity against ofloxacin and its complex on xyline-Alcoholic activity test Kidney, liver and serum of these rats were also studied. On the basis of observed result it could be concluded that Co(II)-Ofloxacin complex were found to be non-toxic and more potent than pure Ofloxacin.(1)
We investigated the gas‐phase fragmentation reactions of a series of 2‐aroylbenzofuran derivatives
by electrospray ionization tandem mass spectrometry (ESI‐MS/MS). The most intense fragment
ions were the acylium ions m/z 105 and [M+H–C6H6]+, which originated directly from the
precursor ion as a result of 2 competitive hydrogen rearrangements. Eliminations of CO and CO2
from [M+H–C6H6]+ were also common fragmentation processes to all the analyzed compounds.
In addition, eliminations of the radicals •Br and •Cl were diagnostic for halogen atoms at aromatic
ring A, whereas eliminations of •CH3 and CH2O were useful to identify the methoxyl group
attached to this same ring. We used thermochemical data, obtained at the B3LYP/6‐31+G(d) level
of theory, to rationalize the fragmentation pathways and to elucidate the formation of E, which
involved simultaneous elimination of 2 CO molecules from B.
Objective(s):
Nanotechnology and nanoparticles are increasingly recognized for their potential applications in aerospace engineering, nanoelectronics, and environmental remediation, medicine and consumer products. More importantly is the potential for the application of silver nanoparticles (Ag NPs) in the treatment of diseases that require maintenance of circulating drug concentration or targeting of specific cells or organs the aim of this study was to investigate the possible protective role of Ag NP antioxidative biomarkers in rats. Ag NPs are used to investigate the potential risks for the environment and health.
Materials and Methods:
Rats received Ag NP, 5, 50, 250 and 500 mg/kg/day IP. After two week of treatment, the activity of enzymatic scavengers such as glutathione peroxidase (GPx), superoxide dismutase (SOD) and total antioxidant capacity (TAC) of blood samples were measured.
Results:
Ag NP in 5, 50, 250 and 500 mg/kg reduced activities of CAT, SOD and increased TAC in plasma.
Conclusion:
In this study, Ag NP with 500mg/kg induced activities of CAT, SOD and decreased TAC. It is concluded that antioxidative properties of Ag NP is dose dependent.
Electrochemical, in-vitro in-vivo study of Co (II)-ofloxacin complexIOSR Journals
Ofloxacin complex has been synthesized and screened for its physicochemical, microbial as well as pharmacological activity have been done in solid and aqueous phase. On the basis of elemental analysis, polarographic studies, amperometric titration and IR spectral studies the probable formula for the complex has been determined at 30±1OC and ionic strength of μ= 1.0[KCl]. Raper’s paper disc method was used for microbial study against various pathogenic bacteria and fungi.Invivo syudy of Swiss mice [25-30gm] were used for antibacterial activity against ofloxacin and its complex on xyline-Alcoholic activity test Kidney, liver and serum of these rats were also studied. On the basis of observed result it could be concluded that Co(II)-Ofloxacin complex were found to be non-toxic and more potent than pure Ofloxacin.(1)
We investigated the gas‐phase fragmentation reactions of a series of 2‐aroylbenzofuran derivatives
by electrospray ionization tandem mass spectrometry (ESI‐MS/MS). The most intense fragment
ions were the acylium ions m/z 105 and [M+H–C6H6]+, which originated directly from the
precursor ion as a result of 2 competitive hydrogen rearrangements. Eliminations of CO and CO2
from [M+H–C6H6]+ were also common fragmentation processes to all the analyzed compounds.
In addition, eliminations of the radicals •Br and •Cl were diagnostic for halogen atoms at aromatic
ring A, whereas eliminations of •CH3 and CH2O were useful to identify the methoxyl group
attached to this same ring. We used thermochemical data, obtained at the B3LYP/6‐31+G(d) level
of theory, to rationalize the fragmentation pathways and to elucidate the formation of E, which
involved simultaneous elimination of 2 CO molecules from B.
Objective(s):
Nanotechnology and nanoparticles are increasingly recognized for their potential applications in aerospace engineering, nanoelectronics, and environmental remediation, medicine and consumer products. More importantly is the potential for the application of silver nanoparticles (Ag NPs) in the treatment of diseases that require maintenance of circulating drug concentration or targeting of specific cells or organs the aim of this study was to investigate the possible protective role of Ag NP antioxidative biomarkers in rats. Ag NPs are used to investigate the potential risks for the environment and health.
Materials and Methods:
Rats received Ag NP, 5, 50, 250 and 500 mg/kg/day IP. After two week of treatment, the activity of enzymatic scavengers such as glutathione peroxidase (GPx), superoxide dismutase (SOD) and total antioxidant capacity (TAC) of blood samples were measured.
Results:
Ag NP in 5, 50, 250 and 500 mg/kg reduced activities of CAT, SOD and increased TAC in plasma.
Conclusion:
In this study, Ag NP with 500mg/kg induced activities of CAT, SOD and decreased TAC. It is concluded that antioxidative properties of Ag NP is dose dependent.
Antibacterial Activity of Schiff Bases Derived from OrthoDiaminocyclohexane, ...inventionjournals
Schiff bases (SBs) are known to possess many biological activities. In this paper we will be interested in nine SBs derived from ortho-diaminocyclohexane, meta-phenylenediamine, 1,6-diaminohexane and benzaldehydes variously substituted by nitro group. We had synthesized, characterized and tested these molecules for their antibacterial properties. Herein our study focuses in particular on the determination of quantum descriptors on which observed antibacterial activity depends, in order to be able to predict biological activities in analogue molecule series. Using quantum chemistry methods at B3LYP / 6-31G (d, p) level, we determined for each molecules, theoretical antibacterial potentials that we correlated to the experimental ones. Calculation results showed that, the energy of the Highest Occupied Molecular Orbital (EHOMO), electronegativity (χ) and electronic energy (E), are the best quantum descriptors related to the antibacterial activity values of studied molecules. The correlation coefficient R 2 indicates that 92.1% of the molecular descriptors defining this model are taken into account with a standard deviation of 0.152.The model significance is reflected by Fischer coefficient F = 7.721: Correlation coefficient of cross-validation = 0.88. This model is acceptable with . The values of the pCE50theo/pCE50exp values of the validation set tend to unity
ABSTRACT- Plants of Polygalaceae family are source of several compounds such as xanthones, coumarins, phenols,
triterpenes, steroids, pyrones derivatives and alkaloids. These plants contain chemical compounds with a large spectrum of
biological activities, including anti-depressant and anti-angiogenic. Moutabea guianensis is an Amazonian species
belongs to the Polygalaceae family. In this work, from roots of M. guianensis were isolated a new xanthone,
3,8-dihydroxy-1,2,4,5-tetramethoxyxanthone, named moutabeone D, and one known xanthone, 1,3,5-trihydroxy-2-
methoxyxanthone. Column chromatography on silica gel and semi-preparative HPLC led the isolation of these
compounds. The structures were elucidated by spectroscopic data (HRESIMS, UV, IR, 1D and 2D NMR).
Key-words- Moutabea guianensis, Polygalaceae, Xanthones
Microwave Irradated Synthesis, Characterization and Evaluation for their Antibacterial and Larvicidal Activities of some Novel Chalcone and Isoxazole Substituted 9-Anilino Acridines
In Silico Study on Tea Flavanoids as Anticlastogens by Manash Pratim Sarma in Advancements in Bioequivalence & Bioavailability
The interaction of flavonoids of tea extract with different histone proteins member of bone marrow of Swiss mice in silico were satisfactory, and all the interaction (Docking using Hex 5.1) were found to have very low entropy values indicative of strong interaction.
Antibacterial Activity of Schiff Bases Derived from OrthoDiaminocyclohexane, ...inventionjournals
Schiff bases (SBs) are known to possess many biological activities. In this paper we will be interested in nine SBs derived from ortho-diaminocyclohexane, meta-phenylenediamine, 1,6-diaminohexane and benzaldehydes variously substituted by nitro group. We had synthesized, characterized and tested these molecules for their antibacterial properties. Herein our study focuses in particular on the determination of quantum descriptors on which observed antibacterial activity depends, in order to be able to predict biological activities in analogue molecule series. Using quantum chemistry methods at B3LYP / 6-31G (d, p) level, we determined for each molecules, theoretical antibacterial potentials that we correlated to the experimental ones. Calculation results showed that, the energy of the Highest Occupied Molecular Orbital (EHOMO), electronegativity (χ) and electronic energy (E), are the best quantum descriptors related to the antibacterial activity values of studied molecules. The correlation coefficient R 2 indicates that 92.1% of the molecular descriptors defining this model are taken into account with a standard deviation of 0.152.The model significance is reflected by Fischer coefficient F = 7.721: Correlation coefficient of cross-validation = 0.88. This model is acceptable with . The values of the pCE50theo/pCE50exp values of the validation set tend to unity
ABSTRACT- Plants of Polygalaceae family are source of several compounds such as xanthones, coumarins, phenols,
triterpenes, steroids, pyrones derivatives and alkaloids. These plants contain chemical compounds with a large spectrum of
biological activities, including anti-depressant and anti-angiogenic. Moutabea guianensis is an Amazonian species
belongs to the Polygalaceae family. In this work, from roots of M. guianensis were isolated a new xanthone,
3,8-dihydroxy-1,2,4,5-tetramethoxyxanthone, named moutabeone D, and one known xanthone, 1,3,5-trihydroxy-2-
methoxyxanthone. Column chromatography on silica gel and semi-preparative HPLC led the isolation of these
compounds. The structures were elucidated by spectroscopic data (HRESIMS, UV, IR, 1D and 2D NMR).
Key-words- Moutabea guianensis, Polygalaceae, Xanthones
Microwave Irradated Synthesis, Characterization and Evaluation for their Antibacterial and Larvicidal Activities of some Novel Chalcone and Isoxazole Substituted 9-Anilino Acridines
In Silico Study on Tea Flavanoids as Anticlastogens by Manash Pratim Sarma in Advancements in Bioequivalence & Bioavailability
The interaction of flavonoids of tea extract with different histone proteins member of bone marrow of Swiss mice in silico were satisfactory, and all the interaction (Docking using Hex 5.1) were found to have very low entropy values indicative of strong interaction.
Toxic Interaction Mechanism of food Colorant Sunset Yellow with trypsin by Sp...AI Publications
The interaction between food colorant sunset yellow (SY) and trypsin (TRP) was studied by multiple spectroscopic and molecular docking methods and molecular docking simulation under simulated physiological conditions to evaluate the toxic of SY at the protein level. The results showed that SY could effectively quench the endogenous fluorescence of TRP, formed a 1:1 complex. The binding distance (r) between SY and TRP was obtained based on the Förster nonradioactive resonance energy transfer and r was less than 7 nm, which indicated that there was a non-radiative energy transition in the system. The thermodynamic parameters were obtained from the van't Hoff equation, and the Gibbs free energy ΔG<0, indicating that the reaction was spontaneous; ΔH<0, ΔS>0, indicating hydrophobic interaction played a major role in forming the SY-TRP complex. Molecular docking results showed that SY was surrounded by the active amino acid residues Ser195, His57 and Asp102 of TRP, which altered the microenvironment of amino acid residues at the catalytic active center of TRP. Furthermore, as shown by the synchronous fluorescence, UV-Visible absorption and circular dichroism data, SY could lead to the conformational and microenvironmental changes of TRP, which may affect its physiological function.
Comparative Assessment of Total Polyphenols and Antioxidant Activity of Comme...AnuragSingh1049
Green Tea, made from Camellia sinensis plant leaves, is one of the most popular drinks in the world. For the past decades, scientists have studied this plant in terms of potential health benefits. Research has shown that green tea helps prevent stroke, malignancy and infections. In this paper, antioxidant activity and total phenol content of 4 samples of green tea from local Tuzla stores were investigated, of which two were of foreign origin. The antioxidant activity of the samples was analyzed using FRAP and DPPH methods. The obtained results show that the highest content of total phenols and the largest antioxidant capacity has a sample of foreign origin. The content of total phenols in the samples ranges from 60.01 to 79.34 mg GAE/g. The highest FRAP value is 3.34 mmol/g. The antioxidant capacity was also confirmed by the DPPH method. The IC50 value ranges from 0.014 to 0.030 mg/mL.
Ceftriaxone is one of the third generations of cephalosporin antibiotics and commercially found as a sodium salt. The market demand for it is still high in recent years, including in Indonesia. However, there is no local production manufacture yet. A high yield of ceftriaxone sodium would be an advantage in industrial scale. Ceftriaxone was synthesized by reacting 7–amino–3–[(2,5–dihydro–6–hydroxy–2–methyl–5–oxo–1,2,4–triazin–3–yl) thiomethyl] cephalosporanic acid (7-ACT) with 2-Mercaptobenzothiazolyl (Z)-2-(2-Aminothiazole-4-yl)-2-Methoxyimino Acetate (MAEM) then with sodium salt in basic condition. The product was generated by solventing-out using acetone. The products were analyzed by HPLC quantitatively and the structure was confirmed using FTIR, MS and NMR. In this research, the variation in the mole ratio of reactants against the yield of product was evaluated. The result showed that the variations in mole ratio reactants affect the yield production. The higher ratio of MAEM would be the higher yield is obtained. The results show that the yield was 72,17% at mole ratio 1:2 which has 99,32% purity. This result could be a consideration in industrial production scale in ceftriaxone sodium preparation.
This ppt describes elicitation as perspective into plant phytochemicals and functional properties with focus on ultrasound and hydrogen peroxides as elicitors
Oxidative Coupling: A Tranquil Approach for Determination of Selexipag by Vis...Ratnakaram Venkata Nadh
The present study is a first report on development of a spectrophotometric method for determination of selexipag (used to cure pulmonary arterial hypertension) in bulk and tablet formulation and its validation. The basis of the proposed method is formation of a chromophore (of λ max 600 nm) in presence of acidic ferric chloride by oxidative coupling reaction between selexipag and MBTH (3-methylbenzo-thiazolin-2-one hydrazone) solution. Regression analysis (r > 0.999) shows that the plotted calibration curve exhibits good linearity in the studied range of concentration (5 – 30 μg mL-1). As per the existing guidelines of ICH, various parameters of the method were tested for validation. Low values of R.S.D. (< 2%) were observed indicating that the proposed method is reproducible, accurate and precise.
Similar to PSP1 enzymes and metabolism poster (20)
Toxic effects of heavy metals : Lead and Arsenicsanjana502982
Heavy metals are naturally occuring metallic chemical elements that have relatively high density, and are toxic at even low concentrations. All toxic metals are termed as heavy metals irrespective of their atomic mass and density, eg. arsenic, lead, mercury, cadmium, thallium, chromium, etc.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
Phenomics assisted breeding in crop improvementIshaGoswami9
As the population is increasing and will reach about 9 billion upto 2050. Also due to climate change, it is difficult to meet the food requirement of such a large population. Facing the challenges presented by resource shortages, climate
change, and increasing global population, crop yield and quality need to be improved in a sustainable way over the coming decades. Genetic improvement by breeding is the best way to increase crop productivity. With the rapid progression of functional
genomics, an increasing number of crop genomes have been sequenced and dozens of genes influencing key agronomic traits have been identified. However, current genome sequence information has not been adequately exploited for understanding
the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
high-throughput phenotyping has become the major bottleneck restricting crop breeding. Plant phenomics has been defined as the high-throughput, accurate acquisition and analysis of multi-dimensional phenotypes
during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
1. Results and
Discussion
The effect of increased substrate
concentration against inhibition
Tubes C and D shown below in Figure 1
showed the effect of increased substrate
concentration (Tube D – Orange) on the
activity of SDH, when the inhibitor malonate is
present. Tube B acts as a control.
Department of Biosciences
Authors: Rebecca Lindley
Department of Biosciences and Chemistry, Faculty of Health and Wellbeing,
Sheffield Hallam University, Sheffield S1 1WB, United Kingdom
Investigating the effect of temperature, inhibition and coenzyme
addition on enzymatic activity of oxidative metabolism in a liver
homogenate
Materials and
Methods
An enzyme assay was carried out where
liver samples were minced and
homogenised to remove cellular
contents.
Different volumes of sodium succinate,
sodium malonate, NAD+ and phosphate
buffer were added to equal amounts of
tetrazolium red and liver homogenate in
each tube.
Tubes A-F were placed in a water bath
at 37°C, Tube G left at room
temperature and tube H kept at 65°C.
pH was stabilised via the addition of
phosphate buffer to each sample.
Acetone was added to each sample to
stop the reaction . The samples were
then centrifuged at 2,500 rpm at 5
minutes. A spectrophotometer was set
at 440nm and blanked using water in a
glass cuvette. Absorbance of each
sample was measured and recorded.
Conclusions
In conclusion, the higher the temperature the
enzyme is working at, the faster the rate of
enzymatic activity. The addition of substrate will
counteract the effect of malonate as an inhibitor
and increase activity of SDH by approximately
tenfold. The addition of a coenzyme will increase
enzyme activity by approximately fourfold.
Therefore, it is observed that the enzyme SDH
would work fastest and most efficiently at 80°C,
with NAD+ added and with increased substrate.
This experiment therefore determined the effects
of different variables on enzymatic activity and
completed its aim.
References
1. Fernandes, A. S., Pereira, M. M., & Teixeira, M. (2001). The
succinate dehydrogenase from the thermohalophilic bacterium
Rhodothermus marinus: redox-Bohr effect on heme
bL. Journal of bioenergetics and biomembranes, 33(4), 343–
352. https://doi.org/10.1023/a:1010663424846
2. Britannica, T. Editors of Encyclopaedia (2013, May
16). Tricarboxylic acid cycle. Encyclopedia Britannica.
https://www.britannica.com/science/tricarboxylic-acid-cycle
3. Green, J., & Narahara, H. (1980). Assay of succinate
dehydrogenase activity by the tetrazolium method: evaluation
of an improved technique in skeletal muscle fractions. Journal
Of Histochemistry & Cytochemistry, 28(5), 408-412. doi:
10.1177/28.5.696664
Introduction
This aim of this experiment was to investigate
the effects of temperature, coenzyme and
inhibition on the enzyme SDH (Succinate
Dehydrogenase). The hypothesis is that as
temperature increases activity increases until
80°C1 (A S Fernandes, M M Pereira, M Teixera, 2001, which
has been found to be the optimum temperature
for SDH. Addition of malonate should reduce
activity and therefore absorption, and addition
of coenzyme should increase activity.
The image below shows the stages of the TCA
cycle, where SDH catalyses the oxidation of
succinate into fumarate. The TCA cycle occurs
in the matrix of the mitochondria, therefore
liver homogenate was used in this experiment
as the liver has a high density of mitochondria
due to its more frequent contraction than other
organs. Tetrazolium red therefore can be used
to measure rate of enzymatic activity.
Enzymes must work
efficiently for a fast
rate of hydrolysis of
substrate, which is
only possible in
optimum conditions
to avoid
denaturation.
2 (Britannica, T. Editors of Encyclopaedia (2013, May 16))
Figure 1 – An enzyme assay was carried out to
investigate effect of competitive inhibition on activity of
the enzyme SDH, and how increasing substrate
concentration affected inhibition. Standard deviation is
shown in error bars.
Succinate concentration was increased twofold
between tubes C (blue) and D (orange). In
Figure 1, it can be seen that mean absorption
of SDH increases by 10.67x upon doubling
substrate concentration. This supports the
hypothesis made that malonate reduces
activity but is counteracted by increasing
substrate concentration.
Effect of addition of coenzyme
Tubes E and F, in comparison with tubes A
and B, shown below in Figure 2, show that
addition of coenzyme NAD+ increases
activity of the SDH enzyme.
Figure 2 – An enzyme assay was carried out to
investigate the effect of adding the coenzyme NAD+
to the samples. A and E, and B and F can be
compared as they are most otherwise similar
respectively. Standard deviation is shown in error
bars.
E had no substrate so addition of coenzyme
made no difference, however in tube F there
was substrate and addition of NAD+
increased enzyme activity 4.33x. This
supports the hypothesis that increased
concentration of NAD+ increases enzyme
activity. Figure 2 above therefore shows that
SDH activity increases as NAD+
concentration increases.
The effect of temperature on SDH activity
Tubes G and H shown below in Figure 3 highlight
the effect of temperature on enzymatic activity,
low temperature (19°C in tube G) and high
temperature (65°C in tube H). Test tube B acts
as a control.
Figure 3 – An enzyme assay was carried out to
investigate effect of temperature on SDH activity.
Optimum temperature for SDH is 80°C. 1 (A S Fernandes,
M M Pereira, M Teixera, 2001) Standard deviation is shown in
error bars.
As tube H was closer to optimum temperature for
SDH, Figure 3 shows that the closer to optimum
temperature, the faster enzymatic activity as
there is less/ no denaturation of enzymes. At
19°C most, if not all, enzymes are denatured
and therefore non-functional. Figure 3 therefore
supports the hypothesis as it proves that
optimum temperatures increase enzymatic
activity.
0.000
0.050
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0.350
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0.450
Mean
Absorption
at
440nm
Test Tube
B
C
D
0.000
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0.600
Mean
absorption
at
440nm
Test tube
A
B
E
F
0.000
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Mean
`absorption
at
440nm
Test Tube
B
G
H