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Wiley InterScience

Journal of Phycology

Journal of Phycology

Volume 42 Issue 2, Pages 324 - 335

Published Online: 3 Apr 2006

© 2010 Phycological Society of America



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OPTIMIZATION OF IRON-DEPENDENT CYANOBACTERIAL (SYNECHOCOCCUS, CYANOPHYCEAE) BIOREPORTERS TO MEASURE IRON BIOAVAILABILITY1
Christel S. Hassler a , Michael R. Twiss a 2 , R. Michael L. McKay b , and George S. Bullerjahn b
  a Department of Biology, Center for the Environment, Clarkson University, Potsdam, New York 13699, USA
  b Department of Biological Sciences, Bowling Green State University, Bowling Green, Ohio 43403, USA

  1Received 28 June 2005. Accepted 26 December 2005.

  2Author for correspondence: e-mail mtwiss@clarkson.edu.

Copyright © 2006 Phycological Society of America
KEYWORDS
bioavailability • bioreporter • cyano-bacteria • iron • isiAB

ABSTRACT

Complex chemistry and biological uptake pathways render iron bioavailability particularly difficult to assess in natural waters. Bioreporters are genetically modified organisms that are useful tools to directly sense the bioavailable fractions of solutes. In this study, three cyanobacterial bioreporters derived from Synechococcus PCC 7942 were examined for the purpose of optimizing the response to bioavailable Fe. Each bioreporter uses a Fe-regulated promoter (isiAB, irpA and mapA), modulated by distinct mechanisms under Fe deficiency, fused to a bacterial luciferase (luxAB). In order to provide a better understanding of the way natural conditions may affect the ability of the bioreporter to sense iron bioavailability, the effect of relevant environmental parameters on the response to iron was assessed. Optimal conditions (and limits of applicability) for the use of these bioreporters on the field were determined to be: a 12 h (12–24 h) exposure time, temperature of 15°C (15°C–22°C), photon flux density of 100 μmol photons·m−2·s−1 (37–200 lmol photons·m−2·s−1), initial biomass of 0.6–0.8 lg chlorophyll a (chl a)·L−1 (0.3–1.5 lg chl a·L−1) or approximately 105 bioreporter cells·mL−1, high phosphate (10 lM), and low micronutrients (absent). The measured luminescence was optimal with an exogenous addition of 60 lM aqueous decanal substrate allowing a 5 min reaction time in the dark before analysis. This study provides important considerations relating to the optimization in the use of bioreporters under field conditions that can be used for method development of other algal and cyanobacterial bioreporters in aquatic systems.


Received: 28 June 2005; Accepted: 26 December 2005;
DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1529-8817.2006.00203.x About DOI

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