Oncidiinae (Orchidaceae) on the great curve of the Xingu River, Pará state, Brazil.

Among the studies on Orchidaceae in the Amazon, none comprised the region of the Great Curve of the Xingu River, located in the lower Xingu river. The aim of this study was to inventory and taxonomically study the species of Oncidiinae (Orchidaceae) in the Great Curve of the Xingu River, Pará state. The floristic survey was performed in the area of the Belo Monte hydroelectric plant, in the Vitória do Xingu municipality, centrally inserted in the called Great Curve of the Xingu River. Botanical collections were accomplished between June 2011 and December 2013. A total of 27 species of Oncidiinae, distributed in 15 genera, was inventoried in the study area. Notylia Lindl. and Trichocentrum Poepp. & Endl. were the richest genera, with five and four species, respectively, followed by Erycina Lindl., Ionopsis Kunth, Lockhartia Hook., Macradenia R.Br., and Ornithocephalus Hook., with two species each. The remaining eight genera are represented by a single species each in the study area. Morphological descriptions, a key for taxonomic identification, illustrations, and comments on distribution, ecology, phenology and morphology are provided for all inventoried species.

Oncidiinae (Orchidaceae) on the great curve of the Xingu River, Pará state, Brazil / Oncidiinae (Orchidaceae) na volta grande do Rio Xingu, Pará, Brasil

Among the studies on Orchidaceae in the Amazon, none comprised the region of the Great Curve of the Xingu River, located in the lower Xingu river. The aim of this study was to inventory and taxonomically study the species of Oncidiinae (Orchidaceae) in the Great Curve of the Xingu River, Pará state. The floristic survey was performed in the area of the Belo Monte hydroelectric plant, in the Vitória do Xingu municipality, centrally inserted in the called Great Curve of the Xingu River. Botanical collections were accomplished between June 2011 and December 2013. A total of 27 species of Oncidiinae, distributed in 15 genera, was inventoried in the study area. Notylia Lindl. and Trichocentrum Poepp. & Endl. were the richest genera, with five and four species, respectively, followed by Erycina Lindl., Ionopsis Kunth, Lockhartia Hook., Macradenia R.Br., and Ornithocephalus Hook., with two species each. The remaining eight genera are represented by a single species each in the study area. Morphological descriptions, a key for taxonomic identification, illustrations, and comments on distribution, ecology, phenology and morphology are provided for all inventoried species.

Entre os estudos com Orchidaceae na Amazônia, nenhum compreende a região da Volta Grande do rio Xingu, localizada no baixo Xingu. O objetivo deste estudo foi inventariar e estudar taxonomicamente as espécies de Oncidiinae (Orchidaceae) na Volta Grande do rio Xingu, estado do Pará, Brasil. O levantamento florístico foi realizado na área da Usina Hidrelétrica de Belo Monte, no município de Vitória do Xingu, inserido centralmente na chamada Volta Grande do Xingu. Foram realizadas coletas botânicas entre junho de 2011 e dezembro de 2013. Na área de estudo, foram inventariadas 27 espécies de Oncidiinae, distribuídas em 15 gêneros. Notylia Lindl. e Trichocentrum Poepp. & Endl. foram os mais ricos, com cinco e quatro espécies respectivamente, seguidos por Erycina Lindl., Ionopsis Kunth, Lockhartia Hook., Macradenia R.Br., e Ornithocephalus Hook., com duas espécies cada. Os oito gêneros restantes estão representados na área de estudo por uma única espécie. São fornecidas descrições morfológicas, chave taxonômica para identificação, ilustrações e comentários sobre distribuição, ecologia, fenologia e morfologia para todas as espécies inventariadas.

Metabolic and osmoregulatory function at low and high (3800 m) altitude.

Altitude evokes physiological adjustments that include not only respiratory and cardiovascular properties, but also metabolic function, renal and endocrine responses. The purpose of the present study was designed to expand our understanding of the physiological process involved with acclimatisation to high altitude in equids. The study examined temporal effects on metabolic and osmoregulatory function in horses (n = 6) at rest and postexercise at 3800 m. Animals were studied at 225 m (Pb = 743 mmHg) and during a 10 day stay at altitude (Pb = 487 mmHg). Rest samples were taken 90 min postprandial at 0830 h and immediately after the gallop phase of a standard exercise test. Changes in glucose, insulin, cortisol, thyroxine, sodium, potassium, chloride and total protein were assessed at both altitudes. Exercise stimulated increases in cortisol, thyroxine, potassium, and chloride; while the concentrations of glucose, insulin, sodium and total protein (regardless of altitude) decreased. Acute (Day 2) altitude exposure (following transport stress) produced significant increases in glucose, cortisol, thyroxine, chloride and protein at rest and exercise. All variables (except cortisol) appeared to stabilise by Day 4 of altitude exposure. Observations from these data (coupled with haematological and blood gases data) indicate that equids acutely acclimate within 2-3 days to this altitude.

Cloning and heterologous expression of a gene encoding an alkane-induced extracellular protein involved in alkane assimilation from Pseudomonas aeruginosa.

Pseudomonas aeruginosa PG201 produces a 16-kDa extracellular protein in media containing n-hexadecane as a carbon source but not in media containing glycerol or glucose. This protein was purified, and the N-terminal amino acid sequence was determined. The amino acid composition of the protein was found to be very similar to that of the so-called protein-like activator for n-alkane oxidation (PA) from P. aeruginosa S7B1. This extracellular protein was previously characterized (K. Hisatsuka, T. Nakahara, Y. Minoda, and K. Yamada, Agric. Biol. Chem. 41:445-450, 1977) and found to stimulate the growth of P. aeruginosa on n-hexadecane and to possess emulsifying activity. To study the role(s) of the PA protein and to make it accessible for possible future applications, we have cloned the PA-encoding (pra) gene and determined its nucleotide sequence. This analysis revealed a protein-coding region of 162 amino acids, with the first 25 residues being reminiscent of those of a typical bacterial signal sequence. The pra gene was inactivated by insertional mutagenesis, and the resulting strain was found to lack extracellular PA protein and to be retarded in its growth in n-hexadecane-containing media. These results are consistent with the growth stimulatory role of the PA protein. The pra gene was expressed in Escherichia coli, and substantial amounts of the recombinant protein were found in the extracellular growth medium. The recombinant protein was purified by metal chelate affinity chromatography. The ability to produce secreted PA protein by E. coli provides a simple and safe means to analyze its function(s) in alkane assimilation in the future.

Isolation and characterization of a regulatory gene affecting rhamnolipid biosurfactant synthesis in Pseudomonas aeruginosa.

A mutant strain (65E12) of Pseudomonas aeruginosa that is unable to produce rhamnolipid biosurfactants and lacks rhamnosyltransferase activity was genetically complemented by using a P. aeruginosa PG201 wild-type gene library. A single complementing cosmid was isolated on the basis of surface tension measurements of subcultures of the transconjugants by using a sib selection strategy. The subcloning of the complementing cosmid clone yielded a 2-kb fragment capable of restoring rhamnolipid biosynthesis, rhamnosyltransferase activity, and utilization of hexadecane as a C source in mutant 65E12. The nucleotide sequence of the complementing 2-kb fragment was determined, and a single open reading frame (rhlR) of 723 bp specifying a putative 28-kDa protein (RhlR) was identified. Sequence homologies between the RhlR protein and some regulatory proteins such as LasR of P. aeruginosa, LuxR of Vibrio fischeri, RhiR of Rhizobium leguminosarum, and the putative activator 28-kDa UvrC of Escherichia coli suggest that the RhlR protein is a transcriptional activator. A putative target promoter which is regulated by the RhlR protein has been identified 2.5 kb upstream of the rhlR gene. Multiple plasmid-based rhlR gene copies had a stimulating effect on the growth of the P. aeruginosa wild-type strain in hexadecane-containing minimal medium, on rhamnolipid production, and on the production of pyocyanin chromophores. Disruption of the P. aeruginosa wild-type rhlR locus led to rhamnolipid-deficient mutant strains, thus confirming directly that this gene is necessary for rhamnolipid biosynthesis. Additionally, such PG201::'rhlR' mutant strains lacked elastase activity, indicating that the RhlR protein is a pleiotropic regulator.

Hydrocarbon assimilation and biosurfactant production in Pseudomonas aeruginosa mutants.

We isolated transposon Tn5-GM-induced mutants of Pseudomonas aeruginosa PG201 that were unable to grow in minimal media containing hexadecane as a carbon source. Some of these mutants lacked extracellular rhamnolipids, as shown by measuring the surface and interfacial tensions of the cell culture supernatants. Furthermore, the concentrated culture media of the mutant strains were tested for the presence of rhamnolipids by thin-layer chromatography and for rhamnolipid activities, including hemolysis and growth inhibition of Bacillus subtilis. Mutant 65E12 was unable to produce extracellular rhamnolipids under any of the conditions tested, lacked the capacity to take up 14C-labeled hexadecane, and did not grow in media containing individual alkanes with chain lengths ranging from C12 to C19. However, growth on these alkanes and uptake of [14C]hexadecane were restored when small amounts of purified rhamnolipids were added to the cultures. Mutant 59C7 was unable to grow in media containing hexadecane, nor was it able to take up [14C]hexadecane. The addition of small amounts of rhamnolipids restored growth on alkanes and [14C]hexadecane uptake. In glucose-containing media, however, mutant 59C7 produced rhamnolipids at levels about twice as high as those of the wild-type strain. These results show that rhamnolipids play a major role in hexadecane uptake and utilization by P. aeruginosa.