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Biomedical subjects

B Gilbert

Publications and source records attributed to B Gilbert.

At least 109 records · Page 6Linked to original sources
PubMed1976

Snail control in urban sites in Brazil with slow-release hexabutyldistannoxane and pentachlorophenol.

Slow release formulations of hexabutyldistannoxane (TBTO) and pentachlorophenol (PCP) were tested for the control of Biomphalaria tenagophila in 52 urban sites in Rio de Janeiro. TBTO acted faster and lasted longer than PCP and at 15 g/m(2) it eliminated snails from 76% of the treated sites for 1 year. Water pollution and rate of flow had no significant influence on the molluscicidal properties of either compound, but alkalinity lowered the activity of TBTO. Failure to control snail populations was due mainly to human interference and to the non-treatment of adjacent breeding sites that were temporarily dry and therefore overlooked.

Animals↗
PubMed1973

Molluscicidal activity of trifenmorph in field trials.

Trifenmorph granules provided 100% control of Biomphalaria glabrata and B. tenagophila when applied at 2 kg of active ingredient per hectare, except at one site with a pH of 5.6 where the snail population was reduced by only 50%. Granulation was found to facilitate application by either hand or mistblower, and reduces the risk of infection to the spray team. Applied to canal margins the granules had a residual toxic effect.

Animals↗
PubMed1973

Field tests of hexabutyldistannoxane (TBTO) in slow-release formulations against Biomphalaria spp.

Hexabutyldistannoxane (TBTO) in an asphalt base was found to retain molluscicidal activity for more than a year in the field. It was not deactivated by immersion in mud or by drying and exposure to the sun. Complete elimination of planorbid snails was achieved and maintained when repopulation pressure was sporadic, but control of a continuously entering population was not practicable. Fixing the product at the site is important, and a formulation in fragments of rubber that floated failed after 1-2 months. TBTO apparently acts cumulatively in snails, but is only initially toxic to aquatic insects and fish, which return to repopulate treated areas that remain snail-free.

Asbestos↗
PubMedDate not supplied

Molecular biology and regulation of methane monooxygenase.

Methanotrophs are ubiquitous in the environment and play an important role in mitigating global warming due to methane. They are also potentially interesting for industrial applications such as production of bulk chemicals or bioremediation. The first step in the oxidation of methane is the conversion to methanol by methane monooxygenase, the key enzyme, which exists in two forms: the cytoplasmic, soluble methane monooxygenase (sMMO) and the membrane-bound, particulate methane monooxygenase (pMMO). This paper reviews the biochemistry and molecular biology of both forms of MMO. In the past few years there have been many exciting new findings. sMMO components have been expressed in heterologous and homologous hosts. The pMMO has been purified and biochemically studied in some detail and the genes encoding the pMMO have been sequenced. Copper ions have been shown to play a key role in regulating the expression of both MMO enzyme complexes. We also present a model for copper regulation based on results from Northern analysis, primer-extensions and new sequence data, and raise a number of unanswered questions for future studies.

Alphaproteobacteria↗
PubMedDate not supplied

Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6.

We have investigated the lipoprotein lipase (LPL) gene of a 2-year-old patient presenting classical features of the familial LPL deficiency including undetectable LPL activity. DNA sequence analysis of exon 5 identified the patient as a homozygote for the Gly188Glu mutation, frequently involved in this disease. A review of cases of LPL deficiency with molecular study of the LPL gene showed a total number of 221 reported mutations involved in this disease. Gly188Glu was involved in 23.5 % of cases and 74.6 % of mutations were clustered in exons 5 and 6. Based on these observations, we propose a method of screening for mutations in this gene.

Amino Acid Substitution↗