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1.
Sci Rep ; 11(1): 5946, 2021 03 15.
Article in English | MEDLINE | ID: mdl-33723271

ABSTRACT

Apis mellifera is an important provider of ecosystem services, and during flight and foraging behaviour is exposed to environmental pollutants including airborne particulate matter (PM). While exposure to insecticides, antibiotics, and herbicides may compromise bee health through alterations of the gut microbial community, no data are available on the impacts of PM on the bee microbiota. Here we tested the effects of ultrapure Titanium dioxide (TiO2) submicrometric PM (i.e., PM1, less than 1 µm in diameter) on the gut microbiota of adult bees. TiO2 PM1 is widely used as a filler and whitening agent in a range of manufactured objects, and ultrapure TiO2 PM1 is also a common food additive, even if it has been classified by the International Agency for Research on Cancer (IARC) as a possible human carcinogen in Group 2B. Due to its ubiquitous use, honey bees may be severely exposed to TiO2 ingestion through contaminated honey and pollen. Here, we demonstrated that acute and chronic oral administration of ultrapure TiO2 PM1 to adult bees alters the bee microbial community; therefore, airborne PM may represent a further risk factor for the honey bee health, promoting sublethal effects against the gut microbiota.


Subject(s)
Bees , Environmental Pollutants/adverse effects , Gastrointestinal Microbiome , Particulate Matter/adverse effects , Titanium/adverse effects , Animals , Biodiversity , Metagenome , Metagenomics/methods , Titanium/chemistry
2.
Mar Genomics ; 37: 1-17, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28970064

ABSTRACT

The biodiversity, ecosystem services and climate variability of the Antarctic continent and the Southern Ocean are major components of the whole Earth system. Antarctic ecosystems are driven more strongly by the physical environment than many other marine and terrestrial ecosystems. As a consequence, to understand ecological functioning, cross-disciplinary studies are especially important in Antarctic research. The conceptual study presented here is based on a workshop initiated by the Research Programme Antarctic Thresholds - Ecosystem Resilience and Adaptation of the Scientific Committee on Antarctic Research, which focussed on challenges in identifying and applying cross-disciplinary approaches in the Antarctic. Novel ideas and first steps in their implementation were clustered into eight themes. These ranged from scale problems, through risk maps, and organism/ecosystem responses to multiple environmental changes and evolutionary processes. Scaling models and data across different spatial and temporal scales were identified as an overarching challenge. Approaches to bridge gaps in Antarctic research programmes included multi-disciplinary monitoring, linking biomolecular findings and simulated physical environments, as well as integrative ecological modelling. The results of advanced cross-disciplinary approaches can contribute significantly to our knowledge of Antarctic and global ecosystem functioning, the consequences of climate change, and to global assessments that ultimately benefit humankind.


Subject(s)
Aquatic Organisms/physiology , Ecosystem , Interdisciplinary Research , Antarctic Regions , Biodiversity , Climate Change , Congresses as Topic , Ecology , Genomics
3.
Adv Microb Physiol ; 69: 187-215, 2016.
Article in English | MEDLINE | ID: mdl-27720011

ABSTRACT

The large diversity of marine microorganisms harboured by oceans plays an important role in planet sustainability by driving globally important biogeochemical cycles; all primary and most secondary production in the oceans is performed by microorganisms. The largest part of the planet is covered by cold environments; consequently, cold-adapted microorganisms have crucial functional roles in globally important environmental processes and biogeochemical cycles cold-adapted extremophiles are a remarkable model to shed light on the molecular basis of survival at low temperature. The indigenous populations of Antarctic and Arctic microorganisms are endowed with genetic and physiological traits that allow them to live and effectively compete at the temperatures prevailing in polar regions. Some genes, e.g. glycosyltransferases and glycosylsynthetases involved in the architecture of the cell wall, may have been acquired/retained during evolution of polar strains or lost in tropical strains. This present work focusses on temperature and its role in shaping microbial adaptations; however, in assessing the impacts of climate changes on microbial diversity and biogeochemical cycles in polar oceans, it should not be forgotten that physiological studies need to include the interaction of temperature with other abiotic and biotic factors.


Subject(s)
Acclimatization/physiology , Bacteria/metabolism , Climate Change , Cold Climate , Ice Cover/microbiology , Microbiota/physiology , Antarctic Regions , Aquatic Organisms/metabolism , Arctic Regions , Ecosystem , Oceans and Seas , Temperature
4.
J Fish Biol ; 76(2): 301-18, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20738709

ABSTRACT

Since haemoglobins of all animal species have the same haem group, differences in their properties, including oxygen affinity, electrophoretic mobility and pH sensitivity, must result from the interaction of the prosthetic group with specific amino-acid residues in the primary structure. For this reason, fish globins have been the subject of extensive studies in recent years, not only for their structural characteristics, but also because they offer the possibility to investigate the evolutionary history of these ancient molecules in marine and freshwater species living in a great variety of environmental conditions. This review summarizes the current knowledge on the structure, function and phylogeny of haemoglobins of notothenioid fishes. On the basis of crystallographic analysis, the evolution of the Root effect is analysed. Adaptation of the oxygen transport system in notothenioids seems to be based on evolutionary changes, involving levels of biological organization higher than the structure of haemoglobin. These include changes in the rate of haemoglobin synthesis or in regulation by allosteric effectors, which affect the amount of oxygen transported in blood. These factors are thought to be more important for short-term response to environmental challenges than previously believed.


Subject(s)
Adaptation, Physiological/physiology , Evolution, Molecular , Hemoglobins/metabolism , Perciformes/classification , Perciformes/physiology , Animals , Environment , Perciformes/metabolism , Phylogeny
5.
Mar Genomics ; 2(1): 67-73, 2009 Mar.
Article in English | MEDLINE | ID: mdl-21798174

ABSTRACT

This review highlights some aspects of the biochemistry of cold-adapted hemoproteins in fish and bacteria, without claiming to be exhaustive. Heme hexacoordination where the sixth ligand is provided by an internal amino-acid residue, in cold-adapted hemoproteins will be discussed.

6.
J Appl Microbiol ; 101(5): 1039-48, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17040228

ABSTRACT

AIMS: The aim of this study was to investigate the lipolytic activity of cold-adapted Antarctic marine bacteria and, furthermore, the combined effect of some environmental factors on this enzymatic process. METHODS AND RESULTS: Strains were assayed for lipolytic activity on a basal medium amended with seven individual fatty acid esters. A significant activity was observed for 148 isolates (95.5% of the total screened). The interactive effect of pH, temperature and NaCl concentration on the substrates was tested for six representative isolates, identified as Pseudoalteromonas, Psychrobacter and Vibrio. Differences between strains according to NaCl and pH tolerances were observed. Only one strain degraded the substrate more efficiently at 4 degrees C than at 15 degrees C. CONCLUSIONS: Our findings demonstrate that the lipolytic activity of Antarctic marine bacteria is rather variable, depending on culture conditions, and occurs in a wide range of salt concentration and pH. SIGNIFICANCE AND IMPACT OF THE STUDY: Isolation and characterization of bacteria that are able to efficiently remove lipids at low temperatures will provide insight into the possibility to use cold-adapted bacteria as a source of exploitable enzymes. Moreover, research on the interactive effects of salt concentration, pH and temperature will be useful to understand the true enzyme potentialities for industrial applications.


Subject(s)
Bacteria/metabolism , Cold Temperature , Lipolysis , Water Microbiology , Adaptation, Physiological , Antarctic Regions , Bacteria/drug effects , Bacteria/enzymology , DNA, Bacterial/genetics , Esterases/metabolism , Hydrogen-Ion Concentration , Lipase/metabolism , Phenotype , Phylogeny , RNA, Ribosomal, 16S/genetics , Sodium Chloride/pharmacology , Species Specificity , Temperature
7.
Neuroscience ; 131(2): 535-46, 2005.
Article in English | MEDLINE | ID: mdl-15708494

ABSTRACT

This study was carried out to identify lamprey neurones relaying trigeminal sensory inputs to reticulospinal cells. Double labeling with fluorescent tracers was used in vitro. Fluorescein-conjugated dextran amines were applied to the proximal stump of the cut trigeminal nerve on both sides, and Texas Red-conjugated dextran amines were injected unilaterally in the middle (MRRN) or the posterior (PRRN) rhombencephalic reticular nuclei. Texas Red retrogradely labeled cells were found ipsi- and contralateral to each injection. Any of these cells with the soma or at least a major dendrite among the fluorescein-labeled trigeminal afferent axons was considered a candidate relay cell. Of these two possibilities, only cells with their soma among the fluorescein-labeled trigeminal afferents were found. The candidate relay cells projecting to the MRRN were mostly clustered at the caudal vestibular nerve level within the trigeminal descending tract, whereas the majority of those projecting to the PRRN were located more caudally. The diameter of candidate relay cells ranged from 9.2 to 24.6 mum and 9.2 to 46.1 mum, after MRRN and PRRN injections, respectively. A possible relay function for these cells was tested with electrophysiological experiments. The intracellular responses to trigeminal nerve stimulation were recorded in reticulospinal cells under control conditions and after ejections of a combination of glutamate ionotropic receptor antagonists over the candidate relay cells in small areas along the sulcus limitans. The synaptic responses elicited in MRRN reticulospinal cells were maximally depressed when ejections were made at the level of the vestibular nerve, in accord with the anatomical data. The synaptic responses in PRRN reticulospinal cells showed maximal depression when ejections were made slightly more caudally. Altogether, these results suggest that cells located within the trigeminal descending tract and projecting to reticular nuclei are likely to be the sensory trigeminal relays to reticulospinal neurones in lampreys.


Subject(s)
Neurons, Afferent/physiology , Petromyzon/physiology , Reticular Formation/physiology , Spinal Cord/physiology , Trigeminal Nerve/physiology , Animals , Neurons, Afferent/cytology , Reticular Formation/cytology , Spinal Cord/cytology , Trigeminal Nerve/cytology
8.
Biophys J ; 81(4): 1938-46, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11566768

ABSTRACT

Hemoglobin function is modulated by several non-heme ligands; among these effectors, organic phosphates generally bind to heterotropic sites with a one-to-one stoichiometry. The phosphate binding site of human hemoglobin is located at the interface between the two beta chains. An additional binding site for polyanions has been studied at the molecular level (Tamburrini, M., A. Riccio, M. Romano, B. Giardina, and G. di Prisco. 2000. Eur. J. Biochem. 267:6089-6098) in the hemoglobins of the south polar skua (Catharacta maccormicki). It is formed by a cluster of six positive charges of both alpha chains (Val-1, Lys-99, Arg-141); the two Lys-99alpha have an essential role in the site structure. The present investigation, carried out on skua deoxyhemoglobins by using a molecular dynamics approach, confirms the structural feasibility of the additional site, possibly having the role of an entry-leaving site, and leads to the proposal of a novel migration pathway for phosphate along the central cavity of hemoglobin from one binding site to the other, occurring according to the hypothesis of a site-site migratory mechanism, which may assign a functional role to the central cavity. The role of Lys-99alpha was further confirmed by molecular dynamics experiments on the mutant Lys-99alpha-->Ala in which, at the end of the simulation, the phosphate was external to the additional site.


Subject(s)
Birds/blood , Hemoglobins/metabolism , Lysine/metabolism , Models, Molecular , Organophosphates/metabolism , Phytic Acid/metabolism , Animals , Binding Sites , Computer Simulation , Hemoglobin A/metabolism , Humans , Kinetics , Lysine/genetics , Macromolecular Substances , Motion , Mutagenesis, Site-Directed/genetics , Protein Structure, Secondary , Species Specificity
9.
Neuroscience ; 104(3): 619-25, 2001.
Article in English | MEDLINE | ID: mdl-11440795

ABSTRACT

In 1937 Papez described an anatomical circuit (or loop) beginning and ending in the hippocampal formation that he proposed subserved emotional experience (Papez, 1937). Specifically, the projections of the circuit were as follows: hippocampal formation--> mammillary bodies--> anterior thalamus--> cingulate cortex--> parahippocampal gyrus--> hippocampal formation. Although the circuit has been refined based on subsequent anatomical findings (Amaral and Witter, 1995; Shibata, 1992; Van Groen and Wyss, 1995), the major links of the circuit unquestionably represent a prominent system of connections in the mammalian brain. Hence, the enduring nature of 'Papez's circuit'. Unlike, however, its persistence as anatomical entity, the proposed functional role for the circuit has been less resilient. The early notion that Papez's circuit subserves emotional experience/expression has been abandoned (LeDoux, 1993) and replaced by the proposal that it is primarily involved in mnemonic functions (Aggleton and Brown, 1999). Lesions of each of the major components of the circuit have been shown to disrupt memory (Aggleton and Brown, 1999; Sutherland et al., 1988; Sziklas and Petrides, 1993). The mammillary bodies represent a major output from the hippocampus in Papez's circuit (Amaral and Witter, 1995). It has recently been shown that cells of mammillary body fire rhythmically in bursts synchronous with the theta rhythm of the hippocampus (Bland et al., 1995; Kirk et al., 1996; Kocsis and Vertes, 1994, 1997) and that this rhythmical activity is dependent upon the action of the hippocampus on the mammillary bodies (Bland et al., 1995; Kirk et al., 1996). It is well established that the mammillary bodies project massively to the anterior thalamus (Shibata, 1992), which taken together with the demonstration that mammillary body cells fire synchronously with theta, suggests that the mammillary bodies may act on the anterior thalamus, possibly in the manner that the hippocampus acts on the mammillary bodies, to rhythmically activate cells of the anterior thalamus at theta frequency. We demonstrated that approximately 75% of cells of the anterior ventral nucleus of the thalamus fire rhythmically synchronous with the hippocampal theta rhythm and the activity of 46% of these anterior ventral neurons was highly correlated with theta. These findings, together with demonstration of theta-rhythmically firing cells in other structures of Papez's circuit, indicate that a theta-rhythmic signal may resonate throughout Papez's circuit, possibly involved in the control of mnemonic functions of the circuit.


Subject(s)
Action Potentials/physiology , Anterior Thalamic Nuclei/physiology , Hippocampus/physiology , Memory/physiology , Neural Pathways/physiology , Neurons/physiology , Theta Rhythm , Animals , Biological Clocks/physiology , Cortical Synchronization , Hippocampus/cytology , Male , Neural Pathways/cytology , Neurons/cytology , Periodicity , Physical Stimulation , Rats , Rats, Sprague-Dawley
10.
Eur J Biochem ; 268(14): 4104-11, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11454005

ABSTRACT

The Gymnothorax unicolor hemoglobin system is characterized by two components, called cathodic and anodic on the basis of their isoelectric point, which were separated by ion-exchange chromatography. The oxygen-binding properties of the purified components were studied in the absence and presence of chloride and/or GTP or ATP in the pH range 6.5-8.0. Stripped cathodic hemoglobin showed a small reverse Bohr effect, high oxygen affinity, and low co-operativity; the addition of chloride only caused a small decrease in oxygen affinity. In the presence of GTP or ATP, the oxygen affinity was dramatically reduced, the co-operativity increased, and the reverse Bohr effect abolished. Stripped anodic hemoglobin is characterized by both low oxygen affinity and co-operativity, and displayed a normal Bohr effect; the addition of chloride increased co-operativity, whereas ATP and GTP significantly modulated oxygen affinity at acidic pH values, enhancing the Bohr effect and giving rise to the Root effect. The complete amino-acid sequences of the alpha and beta chains of both hemoglobins were established; the molecular basis of the functional properties of the hemoglobins is discussed in the light of the primary structure and compared with those of other fish hemoglobins.


Subject(s)
Fishes , Hemoglobins/physiology , Allosteric Regulation , Amino Acid Sequence , Animals , Hemoglobins/chemistry , Molecular Sequence Data , Oxygen/metabolism , Phosphates/metabolism , Sequence Homology, Amino Acid , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
11.
Acta Crystallogr D Biol Crystallogr ; 57(Pt 8): 1144-6, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11468400

ABSTRACT

Liganded and unliganded forms of two Antarctic fish haemoglobins, from Trematomus newnesi and T. bernacchii, have been crystallized in low-salt media using polyethylene glycol as precipitant. In particular, crystals of air-exposed T. newnesi carbomonoxy haemoglobin were found to be isomorphous to the crystals grown in high-salt media. Preliminary X-ray analysis of the diffraction data revealed that the beta-haem iron of this haemoglobin is in the haemichrome state, with both the proximal and distal histidyl residues linked to the iron. This is the first crystallization of a haemichrome intermediate of a vertebrate haemoglobin.


Subject(s)
Hemeproteins/chemistry , Hemoglobins/chemistry , Perciformes , Animals , Antarctic Regions , Crystallization , Crystallography, X-Ray , Ligands , Models, Molecular , Polyethylene Glycols/chemistry , Protein Conformation
12.
Biochemistry ; 40(10): 3062-8, 2001 Mar 13.
Article in English | MEDLINE | ID: mdl-11258920

ABSTRACT

Hemoglobins extracted from fishes that live in temperate waters show little or no dissociation even in the liganded form, unlike human hemoglobin (HbA). To establish whether cold adaptation influences the tendency to dissociate, the dimer-tetramer association constants (L(2,4)) of the carbonmonoxy derivatives of representative hemoglobins from two Antarctic fishes, Trematomus newnesi (Hb1Tn) and Trematomus bernacchii (Hb1Tb), were determined by analytical ultracentrifugation as a function of pH in the range 6.0-8.6 and compared to HbA. HbA is more dissociated than fish hemoglobins at all pH values and in particular at pH 6.0. In contrast, both fish hemoglobins are mostly tetrameric over the whole pH range studied. The extent of hydrophobic surface area buried at the alpha(1)beta(2) interface upon association of dimers into tetramers and the number of hydrogen bonds formed are currently thought to play a major role in the stabilization of the hemoglobin tetramer. These contributions were derived from the X-ray structures of the three hemoglobins under study and found to be in good agreement with the experimentally determined L(2,4) values. pH affects oxygen binding of T. bernacchii and T. newnesi hemoglobins in a different fashion. The lack of a pH effect on the dissociation of the liganded proteins supports the proposal that the structural basis of such effects resides in the T (unliganded) structure rather than in the R (liganded) one.


Subject(s)
Hemoglobins/chemistry , Perciformes/blood , Animals , Carboxyhemoglobin/chemistry , Dimerization , Hemoglobin A/chemistry , Hemoglobins/isolation & purification , Humans , Hydrogen Bonding , Ligands , Protein Structure, Secondary , Solvents , Structure-Activity Relationship , Surface Properties , Ultracentrifugation
13.
Eur J Neurosci ; 13(2): 381-8, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11168543

ABSTRACT

Theta rhythm is most prominent in the hippocampus but has also been recorded in other cortical and limbic structures and can play an important role in functional coupling of widely separated structures responsible for different components of the memory building process. Here we demonstrate in the rat that neuronal activity exhibiting strong state-dependent synchrony with rhythmic hippocampal electroencephalogram is present also at the brainstem level, specifically in the relatively small tegmental nuclei of Gudden intimately connected with the limbic forebrain. We found that during theta states, either occurring spontaneously or triggered by sensory stimulation in the urethane anaesthetized rat, all neurons in the anterior and ventral tegmental nuclei exhibited a consistent switch from irregular discharges to rhythmic bursts. The switch between these patterns closely matched the analogous transformations in the hippocampal EEG, but the level of synchrony between the two signals varied depending on the level of theta activation. During sensory stimulation, when theta is faster and more regular, the rhythmic bursts in the tegmentum showed extremely high coherence (up to 0.96) with hippocampal field potentials. During spontaneous theta, the average coherence was lower but still highly significant (0.62). Gudden's nuclei are reciprocally connected to the mammillary body complex (MB) occupying a strategic position at the gateway of hippocampofugal connections organized in the Papez circuit. Thus, coupling between the MB-Gudden circuit and the hippocampus and consequently the neuronal traffic through the Papez circuit and hence the assembly of limbic structures connected to the hippocampus may vary according to the activity in these specific brainstem nuclei.


Subject(s)
Hippocampus/physiology , Theta Rhythm , Ventral Tegmental Area/physiology , Animals , Behavior, Animal/physiology , Hippocampus/cytology , Mammillary Bodies/cytology , Mammillary Bodies/physiology , Neurons, Afferent/physiology , Periodicity , Rats , Rats, Sprague-Dawley , Ventral Tegmental Area/cytology
14.
Eur J Neurosci ; 12(11): 4081-92, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11069605

ABSTRACT

The role of the mesencephalic locomotor region (MLR) in initiating and controlling the power of swimming was studied in semi-intact preparations of larval and adult sea lampreys. The brain and the rostral portion of the spinal cord were exposed in vitro, while the intact caudal two-thirds of the body swam freely in the Ringer's-containing chamber. Electrical microstimulation (2-10 Hz; 0. 1-5.0 microA) within a small periventricular region in the caudal mesencephalon elicited well-coordinated and controlled swimming that began within a few seconds after the onset of stimulation and lasted throughout the stimulation period. Swimming stopped several seconds after the end of stimulation. The power of swimming, expressed by the strength of the muscle contractions and the frequency and the amplitude of the lateral displacement of the body or tail, increased as the intensity or frequency of the stimulating current were increased. Micro-injection of AMPA, an excitatory amino acid agonist, into the MLR also elicited active swimming. Electrical stimulation of the MLR elicited large EPSPs in reticulospinal neurons (RS) of the middle rhombencephalic reticular nucleus (MRRN), which also displayed rhythmic activity during swimming. The retrograde tracer cobalt-lysine was injected into the MRRN and neurons (dia. 10-20 microm) were labelled in the MLR, indicating that this region projects to the rhombencephalic reticular formation. Taken together, the present results indicate that, as higher vertebrates, lampreys possess a specific mesencephalic region that controls locomotion, and the effects onto the spinal cord are relayed by brainstem RS neurons.


Subject(s)
Mesencephalon/physiology , Motor Activity/physiology , Neurons/physiology , Animals , Brain Mapping , Electric Stimulation , Electromyography , Lampreys , Larva , Mesencephalon/growth & development , Microinjections , Motor Activity/drug effects , Movement/physiology , Neurons/drug effects , Swimming , alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid/administration & dosage , alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid/pharmacology
15.
Biochim Biophys Acta ; 1543(1): 11-23, 2000 Nov 30.
Article in English | MEDLINE | ID: mdl-11087937

ABSTRACT

In order to study the molecular mechanisms of enzyme cold adaptation, direct amino acid sequence, catalytic features, thermal stability and thermodynamics of the reaction and of heat inactivation of L-glutamate dehydrogenase (GDH) from the liver of the Antarctic fish Chaenocephalus aceratus (suborder Notothenioidei, family Channichthyidae) were investigated. The enzyme shows dual coenzyme specificity, is inhibited by GTP and the forward reaction is activated by ADP and ATP. The complete primary structure of C. aceratus GDH has been established; it is the first amino acid sequence of a fish GDH to be described. In comparison with homologous mesophilic enzymes, the amino acid substitutions suggest a less compact molecular structure with a reduced number of salt bridges. Functional characterisation indicates efficient compensation of Q(10), achieved by increased k(cat) and modulation of S(0.5), which produce a catalytic efficiency at low temperature very similar to that of bovine GDH at its physiological temperature. The structural and functional characteristics are indicative of a high extent of protein flexibility. This property seems to find correspondence in the heat inactivation of Antarctic and bovine enzymes, which are inactivated at very similar temperature, but with different thermodynamics.


Subject(s)
Cold Temperature , Fishes/metabolism , Glutamate Dehydrogenase/metabolism , Acclimatization , Amino Acid Sequence , Amino Acid Substitution , Animals , Antarctic Regions , Enzyme Activation , Enzyme Stability , Glutamate Dehydrogenase/chemistry , Glutamate Dehydrogenase/isolation & purification , Hydrogen-Ion Concentration , Kinetics , Molecular Sequence Data , Molecular Weight , NAD/chemistry , NADP/chemistry , Sequence Alignment , Thermodynamics
16.
J Neurosci ; 20(21): 8169-76, 2000 Nov 01.
Article in English | MEDLINE | ID: mdl-11050140

ABSTRACT

The initiation and control of locomotion largely depend on processing of sensory inputs. The cellular bases of locomotion have been extensively studied in lampreys where reticulospinal (RS) neurons constitute the main descending system activating and controlling the spinal locomotor networks. Ca(2+) imaging and intracellular recordings were used to study the pattern of activation of RS neurons in response to cutaneous stimulation. Pressure applied to the skin evoked a linear input/output relationship in RS neurons until a threshold level, at which a depolarizing plateau was induced, the occurrence of which was associated with the onset of swimming activity in a semi-intact preparation. The occurrence of a depolarizing plateau was abolished by blocking the NMDA receptors that are located on RS cells. Moreover, the depolarizing plateaus were accompanied by a rise in [Ca(2+)](i), and an intracellular injection of the Ca(2+) chelator BAPTA into single RS cells abolished the plateaus, suggesting that the latter are Ca(2+) dependent and rely on intrinsic properties of RS cells. The plateaus were shown to result from the activation of a Ca(2+)-activated nonselective cation current that maintains the cell in a depolarized state. It is concluded that this intrinsic property of the RS neuron is then responsible for the transformation of an incoming sensory signal into a motor command that is then forwarded to the spinal locomotor networks.


Subject(s)
Afferent Pathways/physiology , Efferent Pathways/physiology , Escape Reaction/physiology , Motor Neurons/metabolism , Swimming/physiology , Action Potentials/drug effects , Animals , Brain Stem/physiology , Calcium Signaling/drug effects , Calcium Signaling/physiology , Dizocilpine Maleate/pharmacology , Electromyography , Electrophysiology , Excitatory Amino Acid Antagonists/pharmacology , Flufenamic Acid/pharmacology , Fluorescent Dyes , In Vitro Techniques , Lampreys , Motor Neurons/cytology , Motor Neurons/drug effects , Organic Chemicals , Physical Stimulation , Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors , Skin/innervation , Spinal Cord/physiology , Synapses/physiology
17.
Eur J Biochem ; 267(19): 6089-98, 2000 Oct.
Article in English | MEDLINE | ID: mdl-10998071

ABSTRACT

The amino-acid sequence and the oxygen-binding properties of the two haemoglobins of the Antarctic seabird south polar skua have been investigated. The two haemoglobins showed peculiar functional features, which were probably acquired to meet special needs in relation to the extreme environmental conditions. Both haemoglobins showed a weak alkaline Bohr effect which, during prolonged flight, may protect against sudden and uncontrolled stripping of oxygen in response to acidosis. We suggest that a weak Bohr effect in birds may reflect adaptation to extreme life conditions. The values of heat of oxygenation suggest different functional roles of the two haemoglobins. The experimental evidence suggests that both haemoglobins may bind phosphate at two distinct binding sites. In fact, analysis of the molecular models revealed that an additional phosphate binding site, formed by residues NA1alpha, G6alpha and HC3alpha, is located between the two alpha chains. This additional site may act as an entry/leaving site, thus increasing the probability of capturing phosphate and transferring it to the main binding site located between the two beta chains by means of a site-site migratory mechanism, thereby favouring the release of oxygen. It is suggested that most haemoglobins possess an additional phosphate binding site, having such a role in oxygen transport.


Subject(s)
Birds/blood , Hemoglobins/chemistry , Adaptation, Physiological , Amino Acid Sequence , Animals , Binding Sites , Birds/physiology , Cold Temperature , Flight, Animal/physiology , Hemoglobins/genetics , Hemoglobins/physiology , Models, Molecular , Molecular Sequence Data , Oxygen/metabolism , Oxyhemoglobins/metabolism , Phosphates/metabolism , Phytic Acid/metabolism , Protein Binding , Protein Conformation , Sequence Homology, Amino Acid
18.
Eur J Biochem ; 267(1): 121-31, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10601858

ABSTRACT

The Antarctic psychrotolerant bacterium Psychrobacter sp. TAD1 contains two distinct glutamate dehydrogenases (GDH), each specific for either NADP+ or NAD+. This feature is quite unusual in bacteria, which generally have a single GDH. NADP+-dependent GDH has been purified to homogeneity and the gene encoding GDH has been cloned and expressed. The enzyme has a hexameric structure. The amino acid sequence determined by peptide and gene analyses comprises 447 residues, yielding a protein with a molecular mass of 49 285 Da. The sequence shows homology with hexameric GDHs, with identity levels of 52% and 49% with Escherichia coli and Clostridium symbiosum GDH, respectively. The coenzyme-binding fingerprint motif GXGXXG/A (common to all GDHs) has Ser at the last position in this enzyme. The overall hydrophilic character is increased and a five-residue insertion in a loop between two alpha-helices may contribute to the increase in protein flexibility. Psychrobacter sp. TAD1 GDH apparent temperature optimum is shifted towards low temperatures, whereas irreversible heat inactivation occurs at temperatures similar to those of E. coli GDH. The catalytic efficiency in the temperature range 10-30 degrees C is similar or lower than that of E. coli GDH. Unlike E. coli GDH the enzyme exhibits marked positive cooperativity towards 2-oxoglutarate and NADPH. This feature is generally absent in prokaryotic GDHs. These observations suggest a regulatory role for this GDH, the most crucial feature being the structural/functional properties required for fine regulation of activity, rather than the high catalytic efficiency and thermolability encountered in several cold-active enzymes.


Subject(s)
Gammaproteobacteria/enzymology , Glutamate Dehydrogenase (NADP+)/genetics , Glutamate Dehydrogenase (NADP+)/metabolism , Gram-Negative Aerobic Rods and Cocci/enzymology , Amino Acid Motifs , Amino Acid Sequence , Antarctic Regions , Base Sequence , Cloning, Molecular , Codon/genetics , Enzyme Stability , Glutamate Dehydrogenase (NADP+)/chemistry , Glutamate Dehydrogenase (NADP+)/isolation & purification , Hydrogen-Ion Concentration , Ketoglutaric Acids/metabolism , Kinetics , Molecular Sequence Data , Molecular Weight , NADP/metabolism , Open Reading Frames/genetics , Promoter Regions, Genetic/genetics , Sequence Alignment , Sequence Homology, Amino Acid , Temperature
19.
Comp Biochem Physiol B Biochem Mol Biol ; 122(2): 235-40, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10327612

ABSTRACT

In the framework of a study on molecular adaptations of the oxygen-transport and storage systems to extreme conditions in Antarctic marine organisms, we have investigated the structure/function relationship in Emperor penguin (Aptenodytes forsteri) myoglobin, in search of correlation with the bird life style. In contrast with previous reports, the revised amino acid sequence contains one additional residue and 15 differences. The oxygen-binding parameters seem well adapted to the diving behaviour of the penguin and to the environmental conditions of the Antarctic habitat. Addition of lactate has no major effect on myoglobin oxygenation over a large temperature range. Therefore, metabolic acidosis does not impair myoglobin function under conditions of prolonged physical effort, such as diving.


Subject(s)
Adaptation, Physiological , Birds/physiology , Myoglobin/chemistry , Myoglobin/metabolism , Amino Acid Sequence , Amino Acids/analysis , Animals , Molecular Sequence Data , Myoglobin/isolation & purification , Oxygen/metabolism
20.
J Mol Biol ; 287(5): 897-906, 1999 Apr 16.
Article in English | MEDLINE | ID: mdl-10222199

ABSTRACT

As new structural data have become available, somewhat contrasting explanations of the Root effect in fish haemoglobins (Hb) have been provided. Hb 1 of the Antarctic fish Trematomus newnesi has a nearly pH-independent oxygen affinity, in spite of 95 % sequence identity with Hb 1 of Trematomus (previously named Pagothenia) bernacchii that has a strong Root effect. Here, the 2.2 A R-state structure of Trematomus newnesi Hb 1 is presented. The structure is similar to that of Root effect fish Hbs from Spot and T. bernacchii, suggesting that the differences in the pH dependence cannot be related to the modulation of the R-state. In comparison to T. bernacchii Hb 1, the role of the three mutations Thr41 (C6)alpha-->Ile, Ala97 (G3)alpha-->Ser and His41 (C7)beta-->Tyr at the alpha1beta2-interface is discussed.


Subject(s)
Fishes/blood , Hemoglobins/chemistry , Hemoglobins/metabolism , Animals , Crystallography, X-Ray , Models, Molecular , Protein Conformation , Protein Structure, Tertiary , Sequence Homology, Amino Acid
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