Unit 7: Diversity of Soils & Sediments
LECTURE LEARNING GOALS
1. Define soils and sediment, and contrast the microbes living in each. Explain biogeochemical cycles.
2. Describe the diversity, metabolism & habitat of the five classes of the phylum Proteobacteria, including some common example species.
3. Describe the diversity, metabolism & habitat of the Gram-positive bacteria (phylua Firmicutes & Actinobacteria).
Unit 10: Diversity of Permafrost
LECTURE LEARNING GOALS
1. Describe permafrost, and the microbial diversity of permafrost. Explain how the greatest diversity of Archaea exist in cold environments.
2. Describe the two main Archaeal phyla, and describe example species.
3. Explain how climate change is affecting permafrost and microbial diversity.
Unit 8: Rare and Uncultured Microbes
LECTURE LEARNING GOALS
1. Describe the phyla containing rare bacteria: Deinococcus/Thermus, Chlamydia & Planctomycetes.
2. Describe the sequencing methods used to understand uncultured microbes. Explain the Eocyte hypothesis and how this model differs from the three domain tree of life.
3. For the cultured microbes, describe major characteristics for the 13 bacterial phyla, and explain why some microbe remain uncultivated.
6
Unit 5: Everything is everywhere?
LECTURE LEARNING GOALS
1. State the Baas Becking hypothesis, and describe the environmental traits are the strongest drivers of microbial community.
2. Explain how to measure community dissimilarity. Explain why the Baas Becking hypothesis continues to be tested today.
3. Describe methods to link taxonomic or community structure to function.
Unit 9: Human Microbiome
LECTURE LEARNING GOALS
1. Describe the human microbiome: how many microbes there are, how you get your microbiome, who’s there, and how it changes over time and by region.
2. Describe the domain eukarya. List the five superkingdoms and a few notable species.
3. Explain how the human microbiome is related to health and disease.
Unit 6: Diversity of Microbial Mats
LECTURE LEARNING GOALS
1. Definemicrobialmats.Describethe functional guilds of microbes in the different layers, and how they interact.
2. Foreachofthethreephylaof photosynthetic bacteria, contrast how each fixes C and gains energy and reducing equivalents from light.
3. Forthetwothermophilicbacterialphyla, describe their adaptations to life at high
temperature. Explain how they are primitive and deeply-branching.
Evolution Of Bacteria
Bacteria have existed from very early in the history of life on Earth. Bacteria fossils discovered in rocks date from at least the Devonian Period (419.2 million to 358.9 million years ago), and there are convincing arguments that bacteria have been present since early Precambrian time, about 3.5 billion years ago. Bacteria were widespread on Earth at least since the latter part of the Paleoproterozoic, roughly 1.8 billion years ago, when oxygen appeared in the atmosphere as a result of the action of the cyanobacteria. Bacteria have thus had plenty of time to adapt to their environments and to have given rise to numerous descendant forms.
Kingdom Monera
Bacteria
structure of Bacteria
shapes of Bacteria
reproduction in bacteria
How do Bacteria cause disease?
How can Bacteria work to our benefit?
CYNOBACTERIA
Example of cynobacteria
Cyanobacteria terminology
Actinomycetes
Streptomyces
Functions/Role of actinomycetes
Unit 10: Diversity of Permafrost
LECTURE LEARNING GOALS
1. Describe permafrost, and the microbial diversity of permafrost. Explain how the greatest diversity of Archaea exist in cold environments.
2. Describe the two main Archaeal phyla, and describe example species.
3. Explain how climate change is affecting permafrost and microbial diversity.
Unit 8: Rare and Uncultured Microbes
LECTURE LEARNING GOALS
1. Describe the phyla containing rare bacteria: Deinococcus/Thermus, Chlamydia & Planctomycetes.
2. Describe the sequencing methods used to understand uncultured microbes. Explain the Eocyte hypothesis and how this model differs from the three domain tree of life.
3. For the cultured microbes, describe major characteristics for the 13 bacterial phyla, and explain why some microbe remain uncultivated.
6
Unit 5: Everything is everywhere?
LECTURE LEARNING GOALS
1. State the Baas Becking hypothesis, and describe the environmental traits are the strongest drivers of microbial community.
2. Explain how to measure community dissimilarity. Explain why the Baas Becking hypothesis continues to be tested today.
3. Describe methods to link taxonomic or community structure to function.
Unit 9: Human Microbiome
LECTURE LEARNING GOALS
1. Describe the human microbiome: how many microbes there are, how you get your microbiome, who’s there, and how it changes over time and by region.
2. Describe the domain eukarya. List the five superkingdoms and a few notable species.
3. Explain how the human microbiome is related to health and disease.
Unit 6: Diversity of Microbial Mats
LECTURE LEARNING GOALS
1. Definemicrobialmats.Describethe functional guilds of microbes in the different layers, and how they interact.
2. Foreachofthethreephylaof photosynthetic bacteria, contrast how each fixes C and gains energy and reducing equivalents from light.
3. Forthetwothermophilicbacterialphyla, describe their adaptations to life at high
temperature. Explain how they are primitive and deeply-branching.
Evolution Of Bacteria
Bacteria have existed from very early in the history of life on Earth. Bacteria fossils discovered in rocks date from at least the Devonian Period (419.2 million to 358.9 million years ago), and there are convincing arguments that bacteria have been present since early Precambrian time, about 3.5 billion years ago. Bacteria were widespread on Earth at least since the latter part of the Paleoproterozoic, roughly 1.8 billion years ago, when oxygen appeared in the atmosphere as a result of the action of the cyanobacteria. Bacteria have thus had plenty of time to adapt to their environments and to have given rise to numerous descendant forms.
Kingdom Monera
Bacteria
structure of Bacteria
shapes of Bacteria
reproduction in bacteria
How do Bacteria cause disease?
How can Bacteria work to our benefit?
CYNOBACTERIA
Example of cynobacteria
Cyanobacteria terminology
Actinomycetes
Streptomyces
Functions/Role of actinomycetes
Unit 2: Phylogeny
LECTURE LEARNING GOALS
1. Define phylogeny, and describe what a phylogenetic tree can reveal about the species it models.
2. Describe how to construct a phylogenetic tree, and the complexities that create mistakes.
3. Explain how to root a tree, and contrast how to root the tree of life.
Bacteria are microscopic, single-celled organisms that thrive in diverse environments. These organisms can live in soil, the ocean and inside the human gut. Humans' relationship with bacteria is complex. Sometimes bacteria lend us a helping hand, such as by curdling milk into yogurt or helping with our digestion
Carbon and Energy Sources for Bacterial Growth, Structure of spore, The factors that plays major role for the resistance of Bacterial Spore, Sporulation, Germination
High school biology lesson on bacteria. Covers morphology, metabolism, reproduction, and usefulness of bacteria. Also included, an activity that teaches students the morphology of bacteria. To complete the activity, the teacher should provide each student with 2 poker chips (preferably each should be a different color), one side marked with a sticker. The side with the sticker is the dominant allele, the blank side is the recessive allele. The students must recall how traits are inherited and how organisms express dominant or recessive traits to draw each of their bacteria cells.
Unit 2: Phylogeny
LECTURE LEARNING GOALS
1. Define phylogeny, and describe what a phylogenetic tree can reveal about the species it models.
2. Describe how to construct a phylogenetic tree, and the complexities that create mistakes.
3. Explain how to root a tree, and contrast how to root the tree of life.
Bacteria are microscopic, single-celled organisms that thrive in diverse environments. These organisms can live in soil, the ocean and inside the human gut. Humans' relationship with bacteria is complex. Sometimes bacteria lend us a helping hand, such as by curdling milk into yogurt or helping with our digestion
Carbon and Energy Sources for Bacterial Growth, Structure of spore, The factors that plays major role for the resistance of Bacterial Spore, Sporulation, Germination
High school biology lesson on bacteria. Covers morphology, metabolism, reproduction, and usefulness of bacteria. Also included, an activity that teaches students the morphology of bacteria. To complete the activity, the teacher should provide each student with 2 poker chips (preferably each should be a different color), one side marked with a sticker. The side with the sticker is the dominant allele, the blank side is the recessive allele. The students must recall how traits are inherited and how organisms express dominant or recessive traits to draw each of their bacteria cells.
Biological Classification
This ppt shows the details of biological classification. it gives a brief idea about the five kingdom classification with a detailed description of kingdoms monera, protista and fungi. a detailed description of viruses, viroids, prions and lichens have also been given....
For more details visit my youtube channel: (VIHIRA ACADEMY)
https://www.youtube.com/channel/UCxo06Nj-QWo_7SNvMyDnJCQ?view_as=subscriber
This is the second chapter under the Unit-1 of NEET examination syllabus. It is specially prepared to make the students of the NEET examination score all the possible questions for the chappter.
Instructions and bracket to play Morrill Microbe Madness, a game to review representative organisms from the major phyla of the domain bacteria, part of MICROBIO 480 Microbial Diversity.
Unit 11: Viruses and Prions
LECTURE LEARNING GOALS
1. Define what is a virus, and describe the three theories on the origin of viruses.
2. Define and contrast prions and subviral agents. Explain how they are different from viruses.
3. Explain coronaviruses, the origin of SARS- CoV-2, how it infects cells, and the tools we use to fight the spread of COVID-19.
Unit 4: Biofilms & Motility
LECTURE LEARNING GOALS
• Describethethreetypesofbacterialbiofilm, and how each develop.
• Contrastthedifferentwaysthatmicrobes move using flagella. Explain the ways that bacterial and archaeal flagella are different. Describe non-flagellar movement.
• Giveexamplesofhowmicrobesmovefrom the phyla spirochetes and bacteroidetes.
Unit 3: Microbiology of Early Earth
LECTURE LEARNING GOALS
• Describe the early Earth environment, and prevailing theories for the origins of life.
• Describe the major events in the evolution of cellular life, and when they happened.
• Explain the lines of evidence that lead us to know when early life arose, and the scientific basis behind each line.
Unit 1. How to measure diversity
LECTURE LEARNING GOALS
1. Describe the abundance and diversity of microbes, the “unseen majority”, in all natural and manufactured environments.
2. Explain the common measures of microbial diversity, and how diversity is measured.
3. What is the purpose of diversity?
Learning Objectives:
1. Describe the 8-week CIRTL MOOC, An Introduction to Evidence-Based Undergraduate STEM Teaching.
2. Identify some tools that you can use to improve STEM learning outcomes for undergraduate students.
3. Feel enabled to incorporate one or two new ideas into your teaching.
ANAMOLOUS SECONDARY GROWTH IN DICOT ROOTS.pptxRASHMI M G
Abnormal or anomalous secondary growth in plants. It defines secondary growth as an increase in plant girth due to vascular cambium or cork cambium. Anomalous secondary growth does not follow the normal pattern of a single vascular cambium producing xylem internally and phloem externally.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
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/
ESR spectroscopy in liquid food and beverages.pptxPRIYANKA PATEL
With increasing population, people need to rely on packaged food stuffs. Packaging of food materials requires the preservation of food. There are various methods for the treatment of food to preserve them and irradiation treatment of food is one of them. It is the most common and the most harmless method for the food preservation as it does not alter the necessary micronutrients of food materials. Although irradiated food doesn’t cause any harm to the human health but still the quality assessment of food is required to provide consumers with necessary information about the food. ESR spectroscopy is the most sophisticated way to investigate the quality of the food and the free radicals induced during the processing of the food. ESR spin trapping technique is useful for the detection of highly unstable radicals in the food. The antioxidant capability of liquid food and beverages in mainly performed by spin trapping technique.
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
BREEDING METHODS FOR DISEASE RESISTANCE.pptxRASHMI M G
Plant breeding for disease resistance is a strategy to reduce crop losses caused by disease. Plants have an innate immune system that allows them to recognize pathogens and provide resistance. However, breeding for long-lasting resistance often involves combining multiple resistance genes
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.
Nucleophilic Addition of carbonyl compounds.pptxSSR02
Nucleophilic addition is the most important reaction of carbonyls. Not just aldehydes and ketones, but also carboxylic acid derivatives in general.
Carbonyls undergo addition reactions with a large range of nucleophiles.
Comparing the relative basicity of the nucleophile and the product is extremely helpful in determining how reversible the addition reaction is. Reactions with Grignards and hydrides are irreversible. Reactions with weak bases like halides and carboxylates generally don’t happen.
Electronic effects (inductive effects, electron donation) have a large impact on reactivity.
Large groups adjacent to the carbonyl will slow the rate of reaction.
Neutral nucleophiles can also add to carbonyls, although their additions are generally slower and more reversible. Acid catalysis is sometimes employed to increase the rate of addition.
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.
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.
1. SOILS & SEDIMENTS
Unit 07, 2.25.2021
Reading for today: Brown Ch. 10 & 11
Reading for next class: Brown Ch. 13 & 14
Dr. Kristen DeAngelis
Office Hours by appointment
deangelis@microbio.umass.edu
2. Unit 7: Diversity of Soils & Sediments
LECTURE LEARNING GOALS
1. Define soils and sediment, and contrast
the microbes living in each. Explain
biogeochemical cycles.
2. Describe the diversity, metabolism &
habitat of the five classes of the phylum
Proteobacteria, including some
common example species.
3. Describe the diversity, metabolism &
habitat of the Gram-positive bacteria
(phylua Firmicutes & Actinobacteria).
2
3. Unit 7: Diversity of Soils & Sediments
LECTURE LEARNING GOALS
1. Define soils and sediment, and contrast
the microbes living in each. Explain
biogeochemical cycles.
2. Describe the diversity, metabolism &
habitat of the five classes of the phylum
Proteobacteria, including some
common example species.
3. Describe the diversity, metabolism &
habitat of the Gram-positive bacteria
(phylua Firmicutes & Actinobacteria).
3
4. What is soil?
• A solid matrix that
supports plant
growth
• Minerals, organic
matter & microbes
5. What is soil?
• "Soils are a medium for plant growth"
• Soil can be divided into two broad
groups:
– Mineral soils = Derived from rock weathering
– Organic soils = Derived from sedimentation in
bogs and marshes
• Soils change with time, sun, water, wind,
ice, and living creatures
• Soils take thousands to millions of years to
form
6. Rhizosphere
• The soil directly influenced by plant roots
• Rhizosphere soils have more water,
nutrients, stable pH, microbial biomass
and activity compared to bulk soil
7. Rhizosphere
• Roots change chemical and physical
properties of soils, so are also a route of soil
formation or transformation
• Root exudates (sugars and amino acids),
secretions (waste), sloughed root cells, and
lysates
8. Rhizosphere-specific microbes
• Plant growth promoting rhizobacteria –
diverse, functionally cryptic other than
promoting plant growth
• Mycorrhizal fungi (shown at right) – not
all plants are capable of making
mycorrhizal associations, but these also
tend to be specific
• Root nodule forming bacteria – N
fixation in symbiosis with plants; can be
specific associations (e.g., the
filamentous Actinobacteria Frankia
which forms nodules on alder trees), or
or non-specific associations
8
9. Rhizobium etli
Class Alphaproteobacteria
• N-fixing plant symbiont
– informally known as
rhizobia
– Photo shows root N-fixing
nodules, which are
terminally differentiated
symbiotic associations with
plants
10. Microbial N cycling in soils
• There are 5
movements in the
nitrogen cycle, all
accomplished by
microbes
– Fixation
– Uptake
– Mineralization
– Nitrification
– Denitrification*
10
Industrial N2 fixation
11. Microbial N cycling in soils
• Biogeochemical cycles map the transformations
and movements of an element or compound
through the environment.
• Microbes are responsible for all soil N cycling
– Microbes make soil N available to plants
– Plants get ALL of their nutrients (except C) from soils
• N fixation happens naturally by bacteria, but right
now we are industrially fixing N using the Haber-
Bosch process
– As much N enters the atmosphere through industrial
fixation as through biotic routes
11
12. Maritan Soils
• There is evidence of water on Mars
• There are iron minerals like on Earth
• No microbes or evidence of them
found on Mars… yet!
12
13. Sediments
• Soil transported by
water (fluvial
processes), wind
(aeolian processes)
and ice (glaciers)
– deposition on land
forms soil, which takes
thousands to millions of
years per centimeter
depth.
– may eventually
become sedimentary
rock.
14. Activity for Review of
Unit 07.1
• How are soil and sediment related?
• What is the name for soil influenced by
plant roots?
14
15. Unit 7: Diversity of Soils & Sediments
LECTURE LEARNING GOALS
1. Define soils and sediment, and contrast
the microbes living in each. Explain
biogeochemical cycles.
2. Describe the diversity, metabolism &
habitat of the five classes of the phylum
Proteobacteria, including some
common example species.
3. Describe the diversity, metabolism &
habitat of the Gram-positive bacteria
(phylua Firmicutes & Actinobacteria).
15
18. Phylum Proteobacteria
• Most of the familiar gram-negative bacteria are
proteobacteria
• This is a “very successful” phylum because of the
tremendous phylogenetic diversity of its members.
– Each of the five classes of proteobacteria (alpha, beta,
gamma, delta and epsilon) is as diverse as any other
bacterial phyla.
• They have a wide range of phenotypes scattered
across the phylogenetic tree.
• They are named for the shape-shifting sea god
Proteus, because these organisms have evolved so
many phenotypes.
19. Class Alphaproteobacteria
• wide diversity of organisms, including
– Purple non-sulfur phototrophic bacteria
– Heterotrophs
– Pathogens
– Autotrophic methane oxidizers (methylotrophs)
• Metabolism: Autotrophs fix C by the Calvin cycle
• Habitat of this class ranges extensively, but these
organisms dominate in soils and sediments
• Examples
– Caulobacter crescentus
– Wolbachia spp.
– Rhizobium etli
– Mitochondria
20. Wolbachia pipientis
Class Alphaproteobacteria
• Common intracellular
symbiont of arthropods and
nematodes
– Up to 60% of all insects are
infected with Wolbachia
– Maternally transmitted
– tends to not naturally infect
Aedes aegypti, the mosquito
that carries infectious diseases
like dengue virus
• Mosquitos infected with
Wolbachia have a reduced
ability to carry viruses. Fig 10.7. wasp egg infected with
Wolbachia, which are the white
dots at the bottom of the image
21. Mitochondria
Class Alphaproteobacteria
• Order Rickettsiales
• Has DNA, performs
respiration, has an
electron transport system
that occurs across
membranes, and
produces ATP
• endosymbiotic theory
– once was a bacterial cell
that colonized a eukaryote
– Mitochondria originated as
a symbiosis between
separate single-celled
organisms
22. Class Betaproteobacteria
• Large and diverse
• Metabolism
– Chemolithoautotrophs or
heterotrophs, and some pathogens
– Aerobic or facultative anaerobic
– Members can degrade compounds
involved in “waste management,”
including lignin and phenol
• Habitat: most environments,
especially organic-rich soils,
sediments, wastewater, and
eutrophic aquatic systems
23. Ralstonia solanacearum
Class Betaproteobacteria
• Plant pathogen
– Bacterial wilt disease in crops
– tobacco, potato, tomato, pepper,
and bananas
• Obligately anaerobic motile rods
• Infects through the root hairs,
grows, and is transported around
the plant through the xylem
– This pathogen grows in such
abundance that the diagnostic test
is to dip the cut end of an infected
plant in water
– the infection can be seen as a milky
stream flowing out of the xylem
(shown at right)
24. Class Gammaproteobacteria
• A very large and diverse class
• Metabolism
– obligate aerobes, facultative anaerobes, microaerophiles,
and obligate anaerobes
– Heterotrophs, chemoautotrophs and photoautotrophs
• Habitat
– Pathogens, opportunistic pathogens, and symbionts
– Cryophiles, mesophiles, and moderate thermophiles
• Examples
– Escherichia coli
– Chromatium spp.
25. Escherichia coli
Class Gammaproteobacteria
• Facultative anaerobe
• Common in animal feces,
lower intestines of mammals,
and even on the edge of hot
springs
– Routinely used as a fecal
indicator for contamination in
food and water
• Opportunistic pathogen
– E. coli O157:H7 is a strain of the
bacterium E. coli that produces
Shiga-like toxins
– Toxin catalytically inactivates the
ribosome of most eukaryotic cells
– enterohemorrhagic
26. Chromatium spp.
Class Gammaproteobacteria
• Purple sulfur bacteria
– microbial mats
• Motile by polar flagella and
grow alone or in small groups
• May use H2 or sulfide (H2S) as
an electron donor for reverse
electron flow to gain energy
(NADH)
• The product of H2S oxidation is
elemental sulfur, which
accumulates in granules inside
of the cell
27. Class Deltaproteobacteria
• Diversity
– most are anaerobic sulfate reducers
• Metabolism:
– syntrophic hydrogen-generating
heterotrophs
– Also some aerobic heterotrophs
• Habitat: anaerobic sediments and
parasites of other bacteria
• Example species
– Myxococcus xanthus
– Bdellovibrio bacteriovorans
28. Myxococcus xanthus
Class Deltaproteobacteria
• Gliders with complex life
cycles, usually found on
bark or decomposing
leaves or wood
• Produces simple
spheroid fruiting bodies
on short stalks
• Is able to swarm and
excrete lytic and
digestive enzymes that
lyse bacteria
29. Class Epsilonproteobacteria
• Diversity: narrow phylogenetic group
• Habitat: Intestinal symbionts, parasites of
other bacteria, and deep-sea
environments, especially hydrothermal
vents
• Metabolism:
– Microaerophilic or anaerobic heterotrophs
– Generally cannot eat carbohydrates
• Example species
– Helicobacter pylori
30. Helicobacter pylori
Class Epsilonproteobacteria
• Microaerophilic curved rod
with sheathed flagella
• Common symbiont of the
stomach, colonizing ~70%
of humans
• Sometimes can cause
stomach ulcers, but may
also help modulate
stomach acidity so
important to the human
microbiome
31. Helicobacter pylori
• Barry Marshall & Robin Warren won the Nobel prize in 2005 for
establishing the role of H. pylori in stomach ulcers.
• In 1985, Marshall showed that self administration of
Helicobacter pylori causes acute gastritis, and suggested that
chronic colonisation directly leads to peptic ulceration.
• They showed that antibiotic and bismuth salt killed H. pylori
and cured duodenal ulcers.
• This was the first evidence that gastric disorders could be due
to infectious disease.
31
32. Activity for Review of
Unit 07.2
• What microbe is an environmental
biocontrol agent for mosquito-transmitted
viral pathogens?
• What microbe is the ancestor of the
mitochondria?
• What microbe is responsible for ulcers?
• What phylum and class do the purple
sulfur bacteria belong to?
32
33. Unit 7: Diversity of Soils & Sediments
LECTURE LEARNING GOALS
1. Define soils and sediment, and contrast
the microbes living in each. Explain
biogeochemical cycles.
2. Describe the diversity, metabolism &
habitat of the five classes of the phylum
Proteobacteria, including some
common example species.
3. Describe the diversity, metabolism &
habitat of the Gram-positive bacteria
(phylua Firmicutes & Actinobacteria).
33
35. Phylum Firmicutes
• Large & diverse phylum
– aka low G+C Gram positive
bacteria
• Metabolism
– Almost all Heterotrophs
– Anaerobes use substrate-level
phosphorylation rather than
anaerobic respiration
• Habitat: abundant in soils,
also colonize the skin,
mucous membranes & gut
36. Bacillus cereus
Phylum Firmicutes
• Close relative of B.
anthracus
• Soils & guts
• Produces endospores,
stress-resistant asexual
spore that develops
inside mother cells
Fig. 11.3. Bacillus cereus
37. Phylum Actinobacteria
• Diversity spans a small
phylogenetic range but
includes a large number of
families & species
• Metabolism
– Aerobic mesophilic
heterotrophs
– Known antibiotic producers
– These plus Bacillus are the most
common bacterial source of
antibiotics
• Habitat
– Common in soils & guts
– Few animal symbionts and
pathogens
Fig. 11.11. Mycobacterium ulcerans
Fig. 11.12. Thermoleophilium album
38. Streptomyces antibioticus
Phylum Actinobacteria
• Filamentous
growth with
specific spatial
arrangements
• Used in the
industrial
production of
antibiotics
Fig 11.10. Phase-contrast image overlaid with red
(DNA) and green (sporulation septa) fluorescence
39. Mycobacterium tuberculosis
Phylum Actinobacteria
• M. tuberculosis complex (MTC)
– M. africanum, M. bovis, M. canettii,
M. microti, M. tuberculosis (TB).
• Obligate human pathogens with
no environmental reservoir
– One third of people have TB
– Aerosol transmitted
– Treatable with 6 months course of
antibiotics
• MTC’s unique ability to utilize
cholesterol, which is a common
component of human cell
membranes, plays a role in its
persistence
40. Activity for Review of
Unit 07.3 Gram positive bacteria
• For each microbe
listed, name the
phylum it belongs to,
and match it to its
function.
_ Bacillus cereus
_ Mycobacterium
tuberculosis
_ Streptomyces
antibioticus
a. Most common source
of industrial
antibiotics
b. Animal pathogen
with no known
environmental
reservoir
c. Soil microbe that
produces endospores
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41. Unit 7: Soils & Sediments
LECTURE LEARNING GOALS
1. Define soils and sediment, and contrast the
microbes living in each. Explain
biogeochemical cycles.
2. Describe the diversity, metabolism & habitat of
the five classes of the phylum Proteobacteria,
including some common example species.
3. Describe the diversity, metabolism & habitat of
the Gram-positive bacteria (phylua Firmicutes
& Actinobacteria).
Next class is Unit 8: Rare & uncultured microbes
Reading for next class: Brown Ch. 13 & 14
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