| Literature DB >> 23732832 |
Irene Ketseoglou1, Gustav Bouwer.
Abstract
An Anabaena strain (PCC 7120#11) that was genetically engineered to express Bacillus thuringiensis subsp. israelensis cry genes has shown good larvicidal activity against Anopheles arabiensis, a major vector of malaria in Africa. Response surface methodology was used to evaluate the relationship between key growth factors and the volumetric productivity of PCC 7120#11 in an indoor, flat-plate photobioreactor. The interaction of input CO₂ concentration and airflow rate had a statistically significant effect on the volumetric productivity of PCC 7120#11, as did the interaction of airflow rate and photosynthetic photon flux density. Model-based numerical optimization indicated that the optimal factor level combination for maximizing PCC 7120#11 volumetric productivity was a photosynthetic photon flux density of 154 μmol m⁻² s⁻¹ and air enriched with 3.18% (v/v) CO₂ supplied at a flow rate of 1.02 vessel volumes per minute. At the levels evaluated in the study, none of the growth factors had a significant effect on the median lethal concentration of PCC 7120#11 against An. arabiensis larvae. This finding is important because loss of mosquitocidal activity under growth conditions that maximize volumetric productivity would impact on the feasibility of using PCC 7120#11 in malaria vector control programs. The study showed the usefulness of response surface methodology for determination of the optimal growth conditions for a cyanobacterium that is genetically engineered to have larvicidal activity against malaria vectors.Entities:
Keywords: ANOVA; Anabaena PCC 7120#11; Bacillus thuringiensis subsp. israelensis; Bacillus thuringiensis subspecies israelensis; Bti; LC(50); Mosquitocidal; PAR; PPFD; Photobioreactor; RSM; Response surface methodology; analysis of variance; median lethal concentration; photosynthetic photon flux density; photosynthetically active radiation; response surface methodology; revolutions per minute; rpm; vessel volumes per minute; vvm
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Year: 2013 PMID: 23732832 DOI: 10.1016/j.jbiotec.2013.05.012
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307