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2.
AANA J ; 82(1): 20-4, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24654348

ABSTRACT

This case report describes an unexpected event that took place as a result of using improvised equipment. The patient, a 16-year-old female undergoing complex oral surgery, suffered bilateral pneumothorax following the improper use of an airway support device. During the immediate postoperative period with the patient still intubated, oxygen tubing was attached to a right angle elbow connector with the port closed and 10 L/minute oxygen flow was administered to the patient in a manner that did not allow the patient to exhale. Within seconds, pneumothorax was apparent as the patient's vital signs deteriorated, visible swelling was noted in the shoulders and neck, and there was an absence of breath sounds on auscultation. This case study has application beyond the immediate discussion of bilateral pneumothorax, serving as a caution about the unintended consequences of equipment improvisation. In addition to highlighting the hazards of providing patient care with a non-standard device, this study also provides a powerful example of the human factors that can contribute to medical errors in the healthcare setting.


Subject(s)
Chest Tubes , Nurse Anesthetists , Oxygen Inhalation Therapy/adverse effects , Pneumothorax/etiology , Postoperative Complications/etiology , Postoperative Complications/therapy , Adolescent , Female , Humans , Osteotomy, Sagittal Split Ramus , Oxygen Inhalation Therapy/instrumentation
3.
Microb Ecol ; 55(1): 54-64, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17394038

ABSTRACT

Swarming motility is considered to be a social phenomenon that enables groups of bacteria to move coordinately atop solid surfaces. The differentiated swarmer cell population is embedded in an extracellular slime layer, and the phenomenon has previously been linked with biofilm formation and virulence. The gram-negative nitrogen-fixing soil bacterium Rhizobium etli CNPAF512 was previously shown to display swarming behavior on soft agar plates. In a search for novel genetic determinants of swarming, a detailed analysis of the swarming behavior of 700 miniTn5 mutants of R. etli was performed. Twenty-four mutants defective in swarming or displaying abnormal swarming patterns were identified and could be divided into three groups based on their swarming pattern. Fourteen mutants were completely swarming deficient, five mutants showed an atypical swarming pattern with no completely smooth edge and local extrusions, and five mutants displayed an intermediate swarming phenotype. Sequence analysis of the targeted genes indicated that the mutants were likely affected in quorum-sensing, polysaccharide composition or export, motility, and amino acid and polyamines metabolism. Several of the identified mutants displayed a reduced symbiotic nitrogen fixation activity.


Subject(s)
Bacterial Proteins/genetics , Gene Expression Regulation, Bacterial , Movement , Rhizobium etli/genetics , Rhizobium etli/physiology , Bacterial Proteins/metabolism , DNA Transposable Elements/genetics , Mutation , Phaseolus/microbiology , Quorum Sensing/genetics , Rhizobium etli/growth & development , Symbiosis
4.
Biochim Biophys Acta ; 1774(9): 1092-8, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17693143

ABSTRACT

Phylogenetic analysis of the superfamily of D-2-hydroxyacid dehydrogenases identified the previously unrecognized cluster of glyoxylate/hydroxypyruvate reductases (GHPR). Based on the genome sequence of Rhizobium etli, the nodulating endosymbiont of the common bean plant, we predicted a putative 3-phosphoglycerate dehydrogenase to exhibit GHPR activity instead. The protein was overexpressed and purified. The enzyme is homodimeric under native conditions and is indeed capable of reducing both glyoxylate and hydroxypyruvate. Other substrates are phenylpyruvate and ketobutyrate. The highest activity was observed with glyoxylate and phenylpyruvate, both having approximately the same kcat/Km ratio. This kind of substrate specificity has not been reported previously for a GHPR. The optimal pH for the reduction of phenylpyruvate to phenyllactate is pH 7. These data lend support to the idea of predicting enzymatic substrate specificity based on phylogenetic clustering.


Subject(s)
Alcohol Oxidoreductases/metabolism , Alcohol Oxidoreductases/isolation & purification , Amino Acid Sequence , Kinetics , Molecular Sequence Data , Phylogeny , Rhizobium etli/enzymology , Sequence Alignment , Substrate Specificity
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