15 research outputs found
An annotated cDNA library of juvenile Euprymna scolopes with and without colonization by the symbiont Vibrio fischeri
BACKGROUND: Biologists are becoming increasingly aware that the interaction of animals, including humans, with their coevolved bacterial partners is essential for health. This growing awareness has been a driving force for the development of models for the study of beneficial animal-bacterial interactions. In the squid-vibrio model, symbiotic Vibrio fischeri induce dramatic developmental changes in the light organ of host Euprymna scolopes over the first hours to days of their partnership. We report here the creation of a juvenile light-organ specific EST database. RESULTS: We generated eleven cDNA libraries from the light organ of E. scolopes at developmentally significant time points with and without colonization by V. fischeri. Single pass 3' sequencing efforts generated 42,564 expressed sequence tags (ESTs) of which 35,421 passed our quality criteria and were then clustered via the UIcluster program into 13,962 nonredundant sequences. The cDNA clones representing these nonredundant sequences were sequenced from the 5' end of the vector and 58% of these resulting sequences overlapped significantly with the associated 3' sequence to generate 8,067 contigs with an average sequence length of 1,065 bp. All sequences were annotated with BLASTX (E-value < -03) and Gene Ontology (GO). CONCLUSION: Both the number of ESTs generated from each library and GO categorizations are reflective of the activity state of the light organ during these early stages of symbiosis. Future analyses of the sequences identified in these libraries promise to provide valuable information not only about pathways involved in colonization and early development of the squid light organ, but also about pathways conserved in response to bacterial colonization across the animal kingdom
Changes in reflectin protein phosphorylation are associated with dynamic iridescence in squid
Author Posting. © The Author(s), 2009. This is the author's version of the work. It is posted here by permission of The Royal Society for personal use, not for redistribution. The definitive version was published in Journal of The Royal Society Interface 6 (2010): 549-560, doi:10.1098/rsif.2009.0299.Many cephalopods exhibit remarkable dermal iridescence, a component of their complex,
dynamic camouflage and communication. In the species Euprymna scolopes, the light-organ iridescence
is static and is due to reflectin protein-based platelets assembled into lamellar thin-film
reflectors called iridosomes, contained within iridescent cells called iridocytes. Squid in the
family Loliginidae appear to be unique in that the dermis possesses a dynamic iridescent component,
with reflective, colored structures that are assembled and disassembled under the control of
the muscarinic cholinergic system and the associated neurotransmitter acetylcholine (Mathger et
al. 2004). Here we present the sequences and characterization of three new members of the reflectin
family associated with the dynamically changeable iridescence in Loligo and not found in
static Euprymna iridophores. In addition, we show that application of genistein, a protein tyrosine
kinase inhibitor, suppresses acetylcholine- and calcium-induced iridescence in Loligo. We
further demonstrate that two of these novel reflectins are extensively phosphorylated in concert
with the activation of iridescence by exogenous acetylcholine. This phosphorylation and the correlated
iridescence can be blocked with genistein. Our results suggest that tyrosine phosphorylation
of reflectin proteins is involved in the regulation of dynamic iridescence in Loligo.We gratefully acknowledge support from Anteon contract F33615-03-D-5408 to the Marine
Biological Laboratory, Woods Hole, MA and grant # W911NF-06-1-0285 from the Army
Research Office to D.E.M
Cephalopod genomics: a plan of strategies and organization
The Cephalopod Sequencing Consortium (CephSeq Consortium) was established at a NESCent Catalysis Group Meeting, "Paths to Cephalopod Genomics-Strategies, Choices, Organization," held in Durham, North Carolina, USA on May 24-27, 2012. Twenty-eight participants representing nine countries (Austria, Australia, China, Denmark, France, Italy, Japan, Spain and the USA) met to address the pressing need for genome sequencing of cephalopod mollusks. This group, drawn from cephalopod biologists, neuroscientists, developmental and evolutionary biologists, materials scientists, bioinformaticians and researchers active in sequencing, assembling and annotating genomes, agreed on a set of cephalopod species of particular importance for initial sequencing and developed strategies and an organization (CephSeq Consortium) to promote this sequencing. The conclusions and recommendations of this meeting are described in this white paper
Cephalopod genomics : a plan of strategies and organization
© The Author(s), 2012. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Standards in Genomic Sciences 7 (2012): 175-188, doi:10.4056/sigs.3136559.The Cephalopod Sequencing Consortium (CephSeq Consortium) was established at a NESCent Catalysis Group Meeting, “Paths to Cephalopod Genomics- Strategies, Choices, Organization,” held in Durham, North Carolina, USA on May 24-27, 2012. Twenty-eight participants representing nine countries (Austria, Australia, China, Denmark, France, Italy, Japan, Spain and the USA) met to address the pressing need for genome sequencing of cephalopod molluscs. This group, drawn from cephalopod biologists, neuroscientists, developmental and evolutionary biologists, materials scientists, bioinformaticians and researchers active in sequencing, assembling and annotating genomes, agreed on a set of cephalopod species of particular importance for initial sequencing and developed strategies and an organization (CephSeq Consortium) to promote this sequencing. The conclusions and recommendations of this meeting are described in this White Paper.The Catalysis Group Meeting was supported by the National Science Foundation through the National Evolutionary Synthesis Center (NESCent) under grant number NSF #EF-0905606
Research Update: A minimal region of squid reflectin for vapor-induced light scattering
Reflectins are a family of proteins found in the light manipulating cells of cephalopods.
These proteins are made up of a series of conserved repeats that contain highly
represented amino acids thought to be important for function. Previous studies
demonstrated that recombinant reflectins cast into thin films produced structural colors
that could be dynamically modulated via changing environmental conditions. In this study,
we demonstrate light scattering from reflectin films following exposure to a series of
water vapor pulses. Analysis of film surface topography shows that the induction of light
scatter is accompanied by self-assembly of reflectins into micro- and nanoscale features.
Using a reductionist strategy, we determine which reflectin repeats and sub-repeats are
necessary for these events following water vapor pulsing. With this approach, we identify
a singly represented, 23-amino acid region in reflectins as being sufficient to
recapitulate the light scattering properties observed in thin films of the full-length
protein. Finally, the aqueous stability of reflectin films is leveraged to show that
pre-exposure to buffers of varying pH can modulate the ability of water vapor pulses to
induce light scatter and protein self-assembly
Assessment of Biofouling and Corrosion Risk in Tanks Storing B20 Biodiesel
<p>The introduction of next generation renewable fuels to the current infrastructure potentially poses new challenges with regard to biofouling and biocorrosion. In an effort to increase energy independence, the US Department of Defense has mandated the use of next generation alternative fuels. The risk to fuel infrastructure was unknown upon the introduction of B20 (20 percent biodiesel and 80 percent conventional diesel). Three in-ground storage tanks reported as experiencing varying degrees of fouling containing B20 were selected for this study. This work represents a comprehensive attempt to measure the biodeterioration and biofouling of B20 biodiesel and the associated corrosion risk for exposed infrastructure. This knowledge will be used to monitor these activities in service, predict suitable targets for mitigation and assess the efficacy of any mitigation activities deployed.</p
Evaluation of Microbial Corrosion in Biofuel Storage Tanks Using Split-Chamber Zero Resistance Ammetry
Split-chamber zero resistance ammetry (SC-ZRA) was used to study microbiologically influenced corrosion by aerobic chemoorganotrophic microeukaryotes isolated from biodiesel storage tanks. The magnitude and direction of electric current were measured between two shorted carbon steel electrodes, which were deployed in separate chambers connected by a salt bridge (via a SC-ZRA assembly). This approach permitted rapid screening for the corrosive activity of these previously understudied microeukaryotes. During this study, two previously understudied microeukaryotes (Byssochlamys sp. SW2 and Yarrowia lipolytica) showed increased biomass, an increase in electrochemical signal (current), and a corresponding increase in corrosion rate (weight loss). However, other previously understudied microeukaryote (Wickerhammomyces sp. SE3) showed an increase in biomass without an increase in electrochemical signal and minimal corrosion rate, indicating that the SC-ZRA technique can screen for the corrosive activity of a microorganism, regardless of overall microbial activity. This technique could be used to quickly assess the corrosive potential for a range of previously understudied microorganisms
Carbon Catabolite Repression and Impranil Polyurethane Degradation in Pseudomonas protegens Strain Pf-5
Iridescent biofilms of Cellulophaga lytica are tunable platforms for scalable, ordered materials
Abstract Nature offers many examples of materials which exhibit exceptional properties due to hierarchical assembly of their constituents. In well-studied multi-cellular systems, such as the morpho butterfly, a visible indication of having ordered submicron features is given by the display of structural color. Detailed investigations of nature’s designs have yielded mechanistic insights and led to the development of biomimetic materials at laboratory scales. However, the manufacturing of hierarchical assemblies at industrial scales remains difficult. Biomanufacturing aims to leverage the autonomy of biological systems to produce materials at lower cost and with fewer carbon emissions. Earlier reports documented that some bacteria, particularly those with gliding motility, self-assemble into biofilms with polycrystalline structures and exhibit glittery, iridescent colors. The current study demonstrates the potential of using one of these bacteria, Cellulophaga lytica, as a platform for the large scale biomanufacturing of ordered materials. Specific approaches for controlling C. lytica biofilm optical, spatial and temporal properties are reported. Complementary microscopy-based studies reveal that biofilm color variations are attributed to changes in morphology induced by cellular responses to the local environment. Incorporation of C. lytica biofilms into materials is also demonstrated, thereby facilitating their handling and downstream processing, as would be needed during manufacturing processes. Finally, the utility of C. lytica as a self-printing, photonic ink is established by this study. In summary, autonomous surface assembly of C. lytica under ambient conditions and across multiple length scales circumvent challenges that currently hinder production of ordered materials in industrial settings