There are different strategies bacterial cells use to survive. Differentiation can be occasionally one of them. Although differentiation can occur in the bacterial life cycle, it is a strategy to adapt themselves to harsh environments.
Classification of Bacteria microbiologyVinay Dhiman
Based on Bergey's Manual of systematic classification 2nd edition microbiology,Life sciences
The second edition was divided into 5 volumes
The Deinococci , Mollicutes, and Non-proteobacterial Gram-Negative Bacteria
all relevant information that will assist the nurses to acquire the depth knowledge regarding morphological features of bacteria and its subject matter...............
There are different strategies bacterial cells use to survive. Differentiation can be occasionally one of them. Although differentiation can occur in the bacterial life cycle, it is a strategy to adapt themselves to harsh environments.
Classification of Bacteria microbiologyVinay Dhiman
Based on Bergey's Manual of systematic classification 2nd edition microbiology,Life sciences
The second edition was divided into 5 volumes
The Deinococci , Mollicutes, and Non-proteobacterial Gram-Negative Bacteria
all relevant information that will assist the nurses to acquire the depth knowledge regarding morphological features of bacteria and its subject matter...............
General bacteriology / /certified fixed orthodontic courses by Indian dental...Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and offering a wide range of dental certified courses in different formats.
Indian dental academy provides dental crown & Bridge,rotary endodontics,fixed orthodontics,
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General feautures
Sporulation cycle and germination
Genetic elements of bacteria- chromosomes, plasmids, transposable elements, integrons and gene cassettes
differentiation in microbes is a peculiar character, different microbes have a different mode of life some lives as a single cell, and some lives as complex life cycle by having different types of cells, coccoid, rod or sedentary cells it's all depend upon their
General bacteriology / /certified fixed orthodontic courses by Indian dental...Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and offering a wide range of dental certified courses in different formats.
Indian dental academy provides dental crown & Bridge,rotary endodontics,fixed orthodontics,
Dental implants courses.for details pls visit www.indiandentalacademy.com ,or call
00919248678078
General feautures
Sporulation cycle and germination
Genetic elements of bacteria- chromosomes, plasmids, transposable elements, integrons and gene cassettes
differentiation in microbes is a peculiar character, different microbes have a different mode of life some lives as a single cell, and some lives as complex life cycle by having different types of cells, coccoid, rod or sedentary cells it's all depend upon their
This is a research paper I wrote about alternative energy, what it is, why we need it and specific types we can use. I am going to upload this paper to my Wiki, and Weebly site.
This presentation introduces the European Reserarch Centre for Book
and Paper Conservation-Restoration, its projects and further education
courses. Furthermore the studios for conservation are presented and the
possibilies how archives could cooperate with the Centre are listed.
Presentation on genetics of nitrogen fixation by Tahura MariyamTahura Mariyam Ansari
this presentation is about what is the genetics involvement in nitrogen fixation i.e which gene is responsible etc....
the contents include Genetics of N2 fixing microorganisms, Bacterial Nodulation Genes and Regulation of nod Gene Expression, Nif Genes and their Regulation in K. Pneumoniae & Cyanobacteria, Nitrogen fixation mechanism
Nitrogenase Types, Structure and Function, Alternative nitrogenase, Substrate for Nitrogenase, Electron proteins and Hydrogen evolution
Cloning and cDNA Synthesis of PE & PPE Gene of Mycobacterium Strain H37rv5AI Publications
Pathogenic, slow-growing Mycobacterium tuberculosis and other Mycobacterium tuberculosis complex (MTBC) species include the pe/ppe genes. In the pathogen-host connection, these genes are crucial. Despite the fact that the activities of most PE/PPE family proteins are unknown, mounting evidence shows they play a role in M. tuberculosis infection. The role of PE/PPE proteins, which are thought to be involved in the ESX system's action, is investigated. During complicated host-pathogen processes, we also discuss how PE/ PPE proteins are involved in host-pathogen interactions, immune response regulation, and cell fate determination. Finally, we discuss future PE/PPE protein research priorities as well as how present information might be used to develop more accurate diagnostics and vaccines for worldwide TB control. The pe and ppe genes, which are thought to be critical in TB pathogenesis, are only found in mycobacteria. However, nothing is known about how these genes' expression is regulated. Understanding the regulatory control of genes present only in mycobacteria, such as the pe and ppe gene families, might help researchers figure out why the illness is so effective. A transposon mutagenesis method was employed to better understand pe and ppe control. Rv1403c, a previously unknown transcriptional regulator, was discovered as a consequence of this study.
2,4-Dinitrophenol or DNP is a pesticide that disrupts cellular respi.pdfeyeonsecuritysystems
2,4-Dinitrophenol or DNP is a pesticide that disrupts cellular respiration by transporting protons
across cell membranes. What process of cellular respiration does DNP disrupt and why? Could
DNP cause similar damage to a plant if it got inside the plant cell walls?
Solution
DNP acts as a proton ionophore, an agent that can shuttle protons (hydrogen cations) across
biological membranes.
Mitochondria is the power house of the cell and are sites for cellular respiration which generates
fuel for cell activities. In oxidative phosphorylation, the flow of electrons from NADH and
FADH2 to oxygen results in pumping of H+ ions from the matrix to under membrane space.This
gradient of H+ can produce ATP by flowing through ATP synthetase in inner mitochondrial
membrane. DNP disrupts the H+ gradient reducing ATP synthesis.As a result ATP production is
dramatically reduced and energy is thrown off as heat.
An experiment was conducted to determine whether cell wall acts as a barrier to uptake DNP
into cell. It was reported that greater decrease in mutagenicity was observed.Transport of large
DNP molecules across the cell membrane was inhibited to some degree. It is also unknown that
cytochrome P450 major enzyme involved in deactivation of DNP by mamamlian cells, has
similar function in plants. Alao in that study, generation of NADPH by the addition of NADPH
and glucose-6-phosphate did not enhance the deactivation of the DNP. Thus the other enzyme
systems in the plants could be involved.
Further experiments to investigate this is required..
Similar to UW Microbiology Research Paper on Biofilm Formation in P. aeruginosa (20)
2,4-Dinitrophenol or DNP is a pesticide that disrupts cellular respi.pdf
UW Microbiology Research Paper on Biofilm Formation in P. aeruginosa
1. The Role of Phenazines as an Electron Transporter in Pseudomonas aeruginosa Biofilm
and its Effect on Colony Morphology
Huy Pham
Micro 496 Paper
Introduction:
One of the major challenges facing medical care of modern times is chronic infection of
immunocompromised patients by opportunistic pathogens, like pseudomonas. The gram-negative
Pseudomonas aeruginosa is thought to be strictly aerobic, and is known to infect the respiratory
tract of cystic fibrosis patients and persist via development of biofilm. Once established, the
biofilm plays an important role in sheltering the bacterial colony from environmental factors like
desiccation and the host’s immune system. It is noted that oxygen availability at the center of the
biomass (biofilm) is lower than the expected threshold for which strict aerobes can grow (3),
which leads to the question: what factor(s) can account for the thriving of Pseudomonas in
microaerobic conditions?
Biofilm development illustration. D. Davis, 2007
It is a well known phenomena, frequently observed in cystic fibrosis patients, that
pseudomonas in critical mass, form biofilms via quorum-sensing cascades (5), and secrete
2. phenazines into the extracellular environment. A readily observed property of phenazine is its
redox-active toxicity to non-Pseudomonas organisms (4), and can be considered an antibiotic.
Phenazine can also be observed as an active electron transport shuttle in the biomass as well,
which can promote O2-independent survival in microaerobic environments, such as the depths of
the biomass. One area of research is looking at the potential link between pyocyanin, a class of
phenazine, and its role in facilitating pseudomonas respiration in the microaerobic region of
biofilms. In recent studies, it has been shown that mutant Pseudomonas with knockout phenazine
expression (∆-phenazine) generate less robust colonies than its wild-type variant. This result
indicates that phenazine plays a crucial role in the survival and growth of Pseudomonas biomass
via extracellular electron transfer, and contributes to their virulence. This paper will look at
studies that examine the possible association between pyocyanin as an electron transport shuttle,
and the ability of Pseudomonas to persist and grow in a microaerobic environment.
The role of phenazine in bacteria, and pyocyanin in
pseudomonas:
As noted in the review article, “Metabolism and
function of phenazines in bacteria: impacts on the
behavior of bacteria in the environment and biotechnological process,” (5) phenazines are a
group of nitrogen-containing heterocyclic compounds that differ in function and properties based
on type and position of functional groups present. Hundreds of phenazine derivatives have been
identified in nature. Bacteria are the only known producer of phenazine in the natural world.
Derived from the shikimic acid pathway, a highly conserved metabolic feature in most
organisms (5), recent studies on phenazines have shown their role in inducing plant defense
pathways, electron transportation, iron chelation, biofilm formation, and even gene expression.
3. Phenazines are known to form reactive oxygen species, and have been implicated in bacterial
virulence, and can confer competitive advantages over competing organisms as an
antifungal/antibiotic.
The phenazine of interest, pyocyanin, first isolated from patient wounds (5), is
synthesized by the bacterium Pseudomonas aeruginosa, and regulated by quorum sensing
signals. Pyocyanin have been implicated in the inhibition of competing microorganisms during
mixed species lung infections. In addition to acting as a competitive antibiotic, pyocyanin is
found to be secreted into the extracellular region of the pseudomonas biofilm, and research have
assayed its role as an electron transport shuttle, as discussed in the next section.
Studies on pyocyanin as an extracellular electron transport shuttle in Pseudomonas
aeruginosa:
One of the experimental studies that showed how Pseudomonas is able to maintain redox
homeostasis under O2-limited conditions was published in 2007, called, “Pyocyanin Alters
Redox Homeostasis and Carbon Flux through Central Metabolic Pathways in Pseudomonas
aeruginosa.” (6)
In the first part of the study, researchers assayed the oxidized versus reduced state of
pyocyanin as catalyzed by stationary phase LB cultures of Pseudomonas. When left undisturbed
for five minutes, the pyocyanin-laced suspension turned clear, which is indicative of pyocyanin’s
reduced state. When vortexed, the same pyocyanin suspension turned deep blue, which is
indicative of its oxidized state.
4. Left to Right:
Tube 1: Exponential-phase LB culture.
Tube 2: Stationary-phase LB culture, immediately after
removal fromshakingincubator.
Tube 3: Stationary-phase LB culture, left standingat room
temperature for5 minutes.
Tube 4: 100µM pyocyaninin MOPSbuffer.
Tube 5: Same culture as in tubes 2 and3, resuspendedin
buffer showin tube 4 andleft standingat room temperature
Tube 6: Same suspension as in tube 5, aftervortexing
It is noted that at the air-liquid interface, the suspension is always blue, a good
implication of pyocyanin oxidation by O2. This experimental data suggest that pyocyanin in its
clear, reduced state, is oxidized by an abiotic reaction with oxygen, as a result turning blue, and
when left undisturbed for five minutes, is reduced once again to a clear color by the act of
Pseudomonas donating electrons, as demonstrated by Tube 5. This cycle of oxidation and
reduction can be repeated as many times as desired via resting followed by vortexing, as
demonstrated by Tube 6, to show that phenazine is able to continuously cycle between oxidized
and reduced form, thus making it a suitable electron-transporting candidate.
With prior knowledge that NADH reacts with pyocyanin in vitro, researchers
hypothesized that the presence of pyocyanin would decrease intracellular NADH levels. In the
second part of the study, researchers attempt to measure intracellular NADH/NAD+ ratio in wild-
type versus ∆-phenazine mutant, both of which were in stationary growth phase. The
NADH/NAD+ ratio in the wild-type were less than half of that observed in the ∆-phenazine
mutant. After this observation, pyocyanin was added to the ∆-phenazine mutants, resulting in a
decrease of NADH/NAD+ to wild-type level. Knowing that phenazine can accept electrons from
NADH, it can be inferred from these observations that the intracellular NADH/NAD+ ratio is
influenced by the availability of redox reagents.
To further confirm the findings above, the third part of the study involved assaying
NADH/NAD+ ratio and pyocyanin production in an increasingly O2-depleted environment. The
researchers grew batch cultures in a fermentor at 37C, which allowed them to control
5. temperature and aeration of the suspension. As O2 levels plummeted in the wild-type batch,
pyocyanin production sharply increased, and a decrease in NADH/NAD+ followed. The previous
decrease in NADH was not observed in the ∆-phenazine mutant; as O2 plummeted, no pyocyanin
was produced, and NADH/NAD+ remained high. Without phenazine in a hypoxic environment,
it became clear that the cells will not have an electron shuttle for redox activities. The outcomes
of this particular experiment demonstrated the importance of pyocyanin in extracellular redox
activities in hypoxic conditions.
Studies on the pyocyanin effect on biofilm morphology:
The previous study has shown evidence that Pseudomonas is capable of extracellular
redox activity through the usage of pyocyanin as an electron shuttle, but what outcome will this
phenomena have on the properties of biofilm, and how does it affect the virulence of the
pseudomonas colony?
An experimental study published in 2008, “Redox-active antibiotics control gene
expression and community behavior in divergent bacteria,” (2) assayed the morphological aspect
of colony development of various strains of pseudomonas with varying levels of pyocyanin
production. The strains involved in the experiment were: wild-type Pseudomonas aeruginosa
strain 14; ∆-phenazine, which has knockout phenazine-encoding genes; Dianne K. Newman
strain 370 (DKN370), which overproduces phenazine; and two other pseudomonas mutant
strains as explained below.
Pyocyanin, in addition to being a redox reagent, is also responsible for the up-regulation
of over 35 genes (2), including the SoxR and mex operon in pseudomonas, which produces
putative monooxygenase upon activation, and efflux pumps respectively. Given that fact,
6. pyocyanin’s dual role as an extracellular redox reagent and gene expression modulator will
complicate the result in answering the question of how pyocyanin, specifically as an electron
transport shuttle, will directly affect the morphology of the colony. To partially address this
complication, the researchers have included a strain of pseudomonas with SoxR-knockout (∆-
SoxR) and mex-knockout (∆-mex) mutation to partially eliminate gene modulation, and isolate
the electron transport aspect of pyocyanin in the experiment.
35 colonies of each strain was grown on agar plates at room temperature and observed
over eight days. The colony traits observed included surface area coverage, and
wrinkliness/smoothness and pigmentation. Surface area coverage and wrinkliness is an
adaptation to hypoxia (3), and implicative in the reaction of a bacterial colony to oxygen
demand. It is known that oxygen is used up quickly in the colony, and even at shallow depths,
the biofilm environment approaches hypoxia. Given the high organism density and oxygen
demand in the biofilm, the colony arranges itself via quorum sensing factors to maximize oxygen
intake by maximizing surface area exposure. The effect the pigmentation has on the colony
morphology in this experiment is not well understood, and further development is needed to
better understand the mechanisms involved in this expression.
7. The experimental results, as seen above, shows increasing surface area and wrinkliness
of colony morphology as time elapses, though with varying degrees based on strains. The wild-
type colony shows a steady progression towards increasing wrinkliness as cells rearrange
themselves for maximum oxygen exposure. ∆-phenazine exhibit the most advanced wrinkliness
and surface area coverage as it spreads out and tries to compensate for lack of extracellular
electron shuttle. Note that it is evolutionarily undesirable for colonies to exhibit wrinkliness, as it
exacerbates desiccation (3). DKN370, with its overproduction of pyocyanin, stayed the
smoothest. ∆-SoxR and ∆-mex was measured to have released more pyocyanin into the agar than
wild-type, making them behave similarly to the pyocyanin overproducer DKN370. In this
8. experiment, there appears to be a direct correlation between the quantity of extracellular
pyocyanin and colony smoothness, which is inferred to be evolutionarily advantageous in terms
of desiccation resistance and survival in hypoxic environment.
The mechanism dictating the phenotypic effects of pigmentation on the colony
morphology is not well understood (2), but because the ∆-phenazine colony is bright red, and the
pyocyanin overproducer DKN370 is pale, it could be inferred that there is an inverse relationship
between pigment production and pyocyanin secretion. There is much to be researched on such a
relationship before a plausible link can be established.
What can be done to further develop hypothesis:
Given our biochemical understanding of how redox reaction works with phenazine, and
the biological plausibility of pyocyanin’s role as an extracellular electron transporter. It can be
strongly inferred that pyocyanin plays a key role as redox reagent in hypoxic environment, as
demonstrated by the redox assay in the first experiment (6). The second study of the effects of
pyocyanin on colony morphology also supported the extracellular redox reagent hypothesis, but
it also opened up a few unanswered questions.
The second study (2) showed that pseudomonas form more robust biofilms with
heightened expression of extracellular phenazines. Knowing that phenazine has more than one
role in the virulence of pseudomonas, the experiment raises more questions about the actual
mechanism involved in the maintaining robustness of the biofilm: how much of the robustness of
the biofilm is attributable to pyocyanin as an electron transporter, and how much of it due to the
modulation of gene expression as a result of its role as a quorum sensing signal?
Of pyocyanin’s regulation of gene expression in pseudomonas, many up-regulation
pathways are currently not well-understood, such as pigmentation production, and therefore not
9. accounted for, and further advancement is needed to progressively account for the subtle process
in which these genes promote virulence in the organism.
One proposal to indirectly understand the role of pigmentation in the context of gene
regulation is to measure its production in response to various stimuli. An untested hypothesis that
I propose, is that the pigmentation also serve as a response to oxidative stress. There is a
relatively strong association between wrinkliness and pigmentation production that I have
observed from the colony morphology experiment. Perhaps one possible experiment to
determine pigmentation production in response to oxidative stress is to expose strains of
pseudomonas, and their mutant variants, to increasing oxygen saturation, and observe the colony
pigmentation and morphology as time elapses. This experiment may indirectly account for the
role pigmentation play in pseudomonas, and as a result, better resolve the relationship between
exposure to phenazine and colony morphology by ways of better accounting for pigmentation.
Once the up-regulations mechanisms are better mapped out, the experiment may be
improved by introducing new knockout mutations that will more directly assay pyocyanin’s
properties while accounting for its many subtle regulations of gene expression.
Conclusion:
Studies on phenazine as an electron transport and its effect on colony morphology
indicate that there is a causal link between the former and latter. Phenazines are needed as
electron acceptors in hypoxic environments. Pseudomonas colonies that lack pyocyanin cannot
survive well in hypoxic environments, thus forming not-so-robust biofilms that are subject to
desiccation. Multiple studies demonstrate numerous metabolic pathways that involve pyocyanin
beyond the focus of this paper (5), implicating that they serve even more important functions in
the competitive survival of their host than just extracellular electron transport. All of these
10. studies point to a strong association between phenazines and the evolutionary advantage it
confers to biofilm and the virulence of bacterial colonies.
Now that there is strong evidence showing that phenazine promotes virulence in
pseudomonas by ways of redox, the researchers now need to account for the various regulations
of genes under the promotion of pyocyanin. The colony morphology experiment showed not
only results that further support the pseudomonas extracellular electron transport hypothesis, it
also showed pigmentation changes as a secondary effect of pyocyanin production that is yet to be
accounted for. The difficulty in showing the mechanism of the regulation pathways is that we
still do not know much about how the cohorts of operons interact with one another; it is still
work in progress and there is much research to be done in this field.
The ultimate goal of studies in this field is to progress new findings that will better
resolve current questions about pseudomonas virulence, ask better questions about unresolved
operons, and ultimately lead to better antibiotic lines and treatment of immunocompromised
patients. Pyocyanin, as shown by pseudomonas, can be used not unlike penicillin, to inhibit other
organisms from growing (4), and its derivatives holds good potential in medical and industrial
applications.
11. Bibliography
1. D. Davis. “5 Stages of Biofilm Development.” March 2007
Doi:info:doi/10.1371/journal.pbio.0050307.g001
2. Dierich, Lars E. P. et al. “Redox-Active Antibiotics Control Gene Expression and
Community Behavior in Divergent Bacteria.” Science, 29 August 2009; 321(5893); 1203-
1206.
3. Newman, D. K. “From Iron Oxides to Infections: Roles for Redox-Active Antibiotics in
Microbial Survival and Development.” T-639 Auditorium, UW-Seattle. 27 Feb 2012.
Lecture
4. Park, GK et al. “Elucidation of antifungal metabolites produced
by Pseudomonas aurantiaca IB5-10 with broad-spectrum antifungal activity.” J
Microbiology Biotechnology, 2012 Mar; 22(3): 326-30
5. Pierson, Leland S. III et al. “Metabolism and function of phenazines in bacteria: impacts
on the behavior of bacteria in the environment and biotechnological processes.”
Published online at Springerlink.com, 30 March 2010.
6. Price-Whelan, Price et al. “Pyocyanin Alters Redox Homeostasis and Carbon Flux
through Central Metabolic Pathways in Pseudomonas aeruginosa PA14.” Journal of
Bacteriology, 24 May 2007; 189(17):6372.
7. Ramos, Itzel et al. “Phenazines affect biofilm formation by Pseudomonas aeruginosa in
similar ways at various scales.” Res. Microbiol., 16 April 2010; 161(3): 187-191.
8. Wang, Yun et al. “Endogenous Phenazine Antibiotics Promote Anaerobic Survival of
Pseudomonas aeruginosa via Extracellular Electron Transfer.” Journal of Bacteriology,
30 October 2009; 192(1):365.