Red Layer Microbial Observatory Biology In-Lab Workshop Photosynthetic Microbes from Local Rivers & Beyond

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Red Layer Microbial Observatory Biology 507 - In-Lab Workshop Photosynthetic Microbes from Local Rivers & Beyond

Schedule of Activities Session One 1. Microbial Diversity & the RLMO Program 2. Photosynthetic Microbes 3. Mud Enrichment Techniques 4. Microscopic Diversity 75% grade = in-lab projects, Word templates 25% grade = curriculum/application essay

Introduction Microbial Diversity Prokaryotes: Bacteria and Archaebacteria Eukaryotes: Fungi, Algae, and Protozoa

Culture-Dependent Identification Plate, grow, isolate microbes using media Identify isolates - media-based tests Naming traditionally requires pure cultures These approaches grow only 1-5% of what is present naturally in any environment.

Culture-Independent Identification Extract/describe biological molecules e.g. DNA, proteins/enzymes, pigments Apply of specific probes or antibodies (Ab) Assess environment for metabolic processes This workshop combines both culturedependent and -independent approaches.

NSF/MO Enhance awareness of microbial diversity Discover new ways to describe new microbes RLMO - photosynthetic bacteria, Yellowstone MO projects worldwide - soil, open ocean, polar, urban (homeland security issues)

Photosynthetic Microbes Algae - eukaryotic Cyanobacteria - bacteria Purple - bacteria/proteobacteria Green Sulfur - bacteria, unique phylum Green Nonsulfur - bacteria, unique phylum Heliobacteria - bacteria/gram Positive Halophiles - archaea next week Algae/Cyano. = oxygenic; others = anoxygenic

Overall Reaction - Oxygenic/Plant-Like Light + pigment: H2O -> O2 + (H+) + (e-) ATP synthesis via e- transport chain (ETC) ATP used to fix CO2 ( dark reaction ) Summary Reaction H2O + CO2 yields O2 + glucose + ATP We say that this is oxygenic photosynthesis.

Oxygenic Membrane Systems Plants/Algae - chloroplast with thylakoid Cyanobacteria - simple stacks, no organelles Will isolate/assess pigments next time.

Algae Diversity Green - cellulose walls, fresh/marine Euglena - no wall, most fresh Dinoflagellates - cellulose walls, marine - toxins Golden - silica walls, fresh/marine - toxins Brown - cellulose walls, marine Red - cellulose walls, marine Euglena, Dinoflagellates, Golden exist only in unicellular forms - no multicellular.

Cyanobacteria Diversity Widespread habitats - deserts to sea ice Typical bacterial walls - peptidoglycan Unicellular/Non-N2-Fixing - Synechococcus Filamentous/non-N2-Fixing - Oscillatoria Filamentous/N2-Fixing - Anabaena Noteworthy products of some include earthy geosmins, bloom-associated neurotoxins.

Overall Reaction - Anoxygenic Bacteria* Light + pigment: H2S -> S + (H+) + (e-) ATP synthesis via e- transport chain (ETC) ATP used to fix CO2 ( dark reaction ) Summary Reaction H2S + CO2 yields S + glucose + ATP Sulfur tolerate/use HIGH sulfur. Nonsulfur low. *Archaeal photosynthesis TOTALLY different.

Anoxygenic Membrane Systems Purples - lamellae (simple stacks) Green - chlorosomes (vesicles) Heliobacteria - none, all on cell membrane

Purple Bacteria Diversity Anoxic lakes, springs, mud - some thermal High levels H2S (sulfur) or lower (nonsulfur) MANY shapes - cocci, rods, spirilla, ovals e.g. genus - Rhodospirillum

Green Sulfur Diversity Anoxic sulfur lakes, sediments - few thermal MANY shapes - cocci, rods, ovals e.g. genus - Chlorobium

Green Nonsulfur Diversity Hot spring mats, marine salt marshes All filamentous, with cells being large rods e.g. genus - Chloroflexus

Heliobacteria (Gram Positive) Diversity Anoxic lakes, sediments - few thermal Closest relatives: Bacillus and Clostridium Rods that, like relatives, form spores Also can ferment chemicals, like relatives

Mud Enrichment Techniques Winogradsky Column 1980s - mud mixed with C source, buffer Packed into graduated cylinder placed in light Sustains oxygenics (top), anoxygenics (middle) Sealed Bottles 1 tsp mud plus known media (S or no S) Tightly corked and placed in light

Other Ways to Exclude Oxygen Candle jars - just like they sound Shake tubes - tricky to make, get cultures out of Commercial anaerobic jars - expensive

Microscopy Techniques Standard Wet Mount Agents live, applied with liquid to slide/coverslip No need for stain - agents pigments, large Algae, Cyanobacteria - use 20-40X objective Fixed Slides/Simple Stain Agents dead, dried and heated to just slide Agents extremely small, pigment light Other prokaryotes - need oil/100x