2.1.5. Role of Siderophore in metal remediation:
Siderophores are low-molecular mass (400–1,000 Daltons) compounds with high association constants for complexing iron, but they can also form stable complexes with other metals, such as Al, Cd, Cu, Ga, In, Pb and Zn (Glick and Bashan, 1997; Schalk et al., 2011). Although siderophores contain other functional groups, they are broadly classified into three main groups based on the chemical nature of the moieties donating the oxygen ligands for Fe(III) coordination, which are either of the catecholates (enterobactin), hydroxamates (desferrioxamines), or (α-hydroxy-)carboxylates (aerobactin).
Microbes synthesize chelating agents in the form of siderphores that bind heavy metals and cause an increase in bioavailability through complexation reactions (Gadd, 2010; Rajkumar et al., 2010). Production of siderphores is reported in diverse group of bacteria. However, PGP bacteria are better known for siderphore production in diverse environmental conditions including elevated
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For instance, Joshi and Juwarkar (2009) investigated the immobilization of Cd and Cr after inoculation of EPS producing Azotobacter spp. and found that these isolates were able to bind 15.2 mg g-1 of Cd and 21.9 mg g-1 of Cr. Similarly Gonzalez-Chavez et al. (2004) assessed the ability of arbuscular mycorrhizal fungi (AMF) produced insoluble glycoprotein, glomalin to form complexes with heavy metals and found that up to 4.3 mg Cu, 1.1 mg Pb and 0.1 mg Cd per gram of glomalin could be extracted from metal polluted soils. Since there is a correlation between the amount of glomalin in the soil and the amount of heavy metal bound, AMF strains with significant secretion of glomalin should be more suitable for phytostabilization
The purpose of this lab report is to employ a myriad of skills, tools and, methods learned throughout this semester to perform the appropriate tests for the identification of the assigned unknown bacteria. Add more background information here!!! The most important tools and techniques used during this identification include aseptic technique, microscopic examination and, the use of selective and differential media. Aseptic technique is an important tool for microbiologists. It is imperative that aseptic technique is maintained throughout the length of any test to avoid any cross-contamination that may lead to inaccurate results.
Purpose: To identify an unknown microorganism by performing a series of biochemical tests on a pure bacterial culture. Materials and Methods: Tests: Lactose fermentation: Fermentation makes energy available for use by microorganisms by anaerobic breakdown of carbohydrates. The product can either be an acid or gas. When it is positive, the broth will turn from red to yellow and if gas is present a bubble is formed.
Dalia El-Desoky Organic Chemistry II Lab 05 8 February 2017 Dehydration of 2-methylcyclohexanol Introduction: Dehydration is a common reaction in Organic Chemistry used to produce carbon-carbon double bonds. The dehydration mechanism involves the removal of water from an alcohol to form an alkene. In this experiment, 2-methylcyclohexanol will undergo acid catalyzed dehydration in heat to form three products: 1-methylcyclohexene, 3-methylcyclohexene, and methylenecyclohexane [1]. The reaction is carried out in a Hickman still filled with Drierite, a drying agent composed of CaSO4 which absorbs water.
Gram-negative bacteria also have a negative charge but get the charge from lipopolysaccharides (Bacterial Morphology). For this experiment, biochemical tests were utilized to help determine which of the following four bacteria were in the unknown test tube number 16: E. coli, E. aerogenes, K. pneumoniae, and S. typhimurium. The unknown bacteria was also inoculated and placed on a TSA plate using the T-Streak method to verify that isolated colonies could be obtained. The biochemical tests that were used were the Citrate test, Methyl Red test, Voges-Proskauer test, Urease test, Sulfur Indole Motility test, and Triple Sugar Iron Agar test.
coli bacteria new traits. The pGLO plasmid that is being transformed into these cells contains genes that can give colonies of bacteria the ability of antibiotic resistance and a green fluorescent glow. Four different models were prepared and plated on multiple agar plate. After the bacteria was grown for three days in an incubator at 37°C; observations were made and recorded (Table 1). All of the plates were looked at for the amount of colonies grown, if growth was present, and if the colonies gained the ability to glow green.
But, since no arabinose was present, the bacteria was unable to glow. In the second dish, +pGLO LB/amp/ara, the bacteria was able to glow and grow since there was the pGLO plasmid which contains the gene that is ampicillin resistant, and the sugar arabinose which activates the araC gene which allows the bacteria to glow. In the third dish, -pGLO LB/amp, the bacteria did not glow or
Introduction Our world is composed of many bacteria’s’ that can either help or destroy us. Therefore, its’s imperative to learn and study them. The purpose of the lab was to put into action the methods that have been learned in the laboratory to determine our unknown bacteria. Bacteria’s can have different features, shapes, and or arrangements that help microbiologist determined their role in our life (whether they are good or bad for humans).
The plate labeled LB/amp/ara: +pGlo had several surviving colonies like the other +pGlo plate, except this time the colonies were a green color and the glowed under a UV light. The glow would be a result of adding the sugar arabinose, which seems to be acting as an inducer in the operon of the bacterium. It can be considered an inducer because in the presence of the arabinose, the colonies glowed, but without it the colonies did not experience any change, leading to the belief that the gene that leads to the green fluorescence is normally turned off. To further the research on the effect of the arabinose on the E. coli, a sample of the bacteria in the LB/amp: +pGlo and placed it in a plate with arabinose lines across the bottom.
In the spot overlay Ames assay in (Table 1) the positive control is mutagenic. The positive control for TA1535 shows that are double the amount of colonies than the negative control but it was expected that the colony count to be higher. The TA1538 does not show it is mutagenic because a possible source error can be the bacteria labels were switched.
rtists dating back to the Prehistoric times, attempted to create human figures. They differ in their reasoning for making them, as well as the style of each one. The Cycladic, Female Figure, 2500-2400 B.C.E., and the Classical, Doryphoros 480-400 BCE by Polykleitos both are examples of how different human statue styles and purposes change between periods. Culture of the Cycladic time period, 2500-2400 BCE, is widely unknown. However, what is known about the Cycladic culture came from Homer's Iliad and the Odyssey.
Only a motile bacteria could travel that far from the center of inoculation. Furthermore, it confirmed that P. vulgaris is a facultative
In addition, the bacteria need arabinose that help activate the protein that allows to glow green in the transformed bacteria cells. To let
The following was eliminated because they are gram positive: Bacillus cereus, Bacillus circulans, Bacillus coagulans, Bacillus megaterium, Bacillus subtilis, Bacillus thuringiensis, Brevibacillus brevis, Geobacillus stereothermophilus, Lysinibacillus sphaericus, Clostridium perfringens, Corynebacterium pseudodiphtheriticum, Listeria monocytogenes, Lactobacillus casei, Enterococcus faecalis (Streptococcus), Streptococcus lactis (Lactococcus), Streptococcus mutans, Streptococcus pneumonia, Micrococcus (Kocuria) roseus, Sarcina lutea (Micrococcus luteus), Sporosarcina ureae, Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus saprophyticus, and Rhodococcus rhodochorous. The remaining microbes are gram negative: Alcaligenes faecalis, Rhizobium radiobacter, Salmonella typi, Serratia marcescens, Shigella flexneri, Yersina pseudotuberculosis, Erwina persicinus, Serratia liquifacens, Halobacter salinarium, Enterobacter aerogenes, Eschirichia coli, Flavobacter capsulatum,
However using bacteriostatic agent can have a reverse effect on bacterial selection of which attributes to damage of bacteria in stress condition. To avoid this effect in FDA BAM, the agent added after 4hrs of incubation to allow the injured cells to recover and grow in media, but in ISO 11290 at first step of enrichment, the half concentration of agent is added. In both media the buffering capacity of media is very high and leads to enhanced cell growth and
Approximately 60-90% of the Gram-positive bacterial cell wall is made up of peptidoglycan and interwoven teichoic acid, while only