Productivity, carbon utilization, and energy content of mass in scalable microalgae systems.

This study was designed to examine carbon utilization within scalable microalgae production systems. Neochloris oleoabundans was produced in replicated troughs containing BG11 nutrient formulation. Atmospheric CO(2) was supplemented with ∼5% CO(2) or with NaHCO(3), and the pH of troughs receiving NaHCO(3) was adjusted with HCl or H(3)PO(4). Peak biomass concentrations reached 950, 1140, or 850 mg L(-1) and biomass productivities of 109, 96, and 74 mg L(-1) day(-1) were achieved in the CO(2), NaHCO(3):HCl and NaHCO(3):H(3)PO(4) troughs, respectively. The highest productivity is expected in a scaled-up continuous batch process of the CO(2) supplemented system, which was projected to yield 8948 L lipids ha(-1)yr(-1). Carbon utilization in the CO(2), NaHCO(3):HCl and NaHCO(3):H(3)PO(4) systems was ∼0.5, 15.5, and 12.9%, while the energy content of the combustible biomass was 26.7, 13.2, and 15.4 MJ kg(-1), respectively. Techno-economic analyses of microalgal production systems should consider efficiencies and cost-benefit of various carbon sources.

Biomass production and nutrient uptake by Neochloris oleoabundans in an open trough system.

The purpose of this paper is to present biomass and nutrient uptake data from Neochloris oleoabundans production in an open trough system. The growth medium used was BG11, temperature ranged from 16.7 °C to 25.3 °C, and pH ranged from 5.52 to 9.94 because the customary pH increase during algal biomass production was moderated by incoming CO(2) gas streams (atmospheric, 2%, 4%, and 6% CO(2)). Peak concentrations of algal biomass ranged from 643 to 970 mg L(-1), specific growth rates ranged from 0.15 to 0.37 day(-1), and doubling times ranged from 4.8 to 1.9 days. Carbon, nitrogen, and phosphorus were incorporated into the biomass at 0.05%, 8.3%, and 54% of supplied amounts. Open growth systems supplemented with CO(2) should be designed to regulate medium pH within the range of 6.3 to 7.1. Future research should examine various media and alternative carbon sources to decrease doubling times, increase peak concentrations, and optimize nutrient uptake.

Using student-generated UV-induced Escherichia coli mutants in a directed inquiry undergraduate genetics laboratory.

We report a thematic sequence of directed inquiry-based labs taking students from bacterial mutagenesis and phenotypic identification of their own self-created mutant, through identification of mutated genes by biochemical testing, to verification of mutant alleles by complementation, and finally to mutant allele characterization by DNA sequence analysis. The lab utilizes UV mutagenesis with wild-type Escherichia coli and a UV-sensitive isogenic derivative optimized for undergraduate use. The labs take advantage of the simplicity of E. coli in a realistic genetic investigation using safe UV irradiation methods for creation and characterization of novel mutants. Assessment data collected over three offerings of the course suggest that the labs, which combine original investigation in a scientifically realistic intellectual environment with learned techniques and concepts, were instrumental in improving students' learning in a number of areas. These include the development of critical thinking skills and understanding of concepts and methods. Student responses also suggest the labs were helpful in improving students' understanding of the scientific process as a rational series of experimental investigations and awareness of the interdisciplinary nature of scientific inquiry.

Characterization of gamma-butyrolactone autoregulatory signaling gene homologs in the angucyclinone polyketide WS5995B producer Streptomyces acidiscabies.

Organisms belonging to the genus Streptomyces produce numerous important secondary metabolites and undergo a sophisticated morphological differentiation program. In many instances these processes are under the control of gamma-butyrolactone (GBL) autoregulatory systems. Streptomyces acidiscabies strain 84.104 produces the secondary metabolite aromatic angucyclinone polyketide WS5995B. In order to explore the role of GBL regulatory circuitry in WS5995B production and morphogenesis in S. acidiscabies, a gene cluster encoding GBL autoregulatory signaling homologs was identified and characterized. Two GBL receptor homologs, sabR and sabS, were found flanking a GBL synthase homolog sabA. Strains carrying mutations in sabS produced elevated levels of WS5995B and displayed conditional morphological defects reminiscent of defects seen in Streptomyces bldA mutants. Notably, sabS possesses a TTA codon predicted to be recognized by tRNA(leu). sabA mutants produced higher levels of WS5995B than the wild-type strain but to a lesser extent than the levels of WS5995B seen in sabS mutants. Purified recombinant SabR and SabS were tested for their abilities to bind predicted AT-rich autoregulatory element (ARE) boxes within the sabRAS region. SabS did not bind any DNA sequences in this region, while SabR bound an ARE box in the region upstream of sabS. Quantitative reverse transcription-PCR analysis revealed higher levels of sabS transcript in sabR mutants than in the wild-type strain, suggesting that sabS expression is repressed by SabR. Based on these data, we propose that the S. acidiscabies sabRAS genes encode components of a signaling pathway which participates in the regulation of WS5995B production and morphogenesis.