Gene expression analysis of a Louisiana native Chlorella vulgaris (Chlorophyta)/Leptolyngbya sp. (Cyanobacteria) co-culture using suppression subtractive hybridization
Document Type
Article
Publication Date
3-1-2013
Abstract
A locally isolated co-culture of two photosynthetic species [Chlorella vulgaris (Chlorophyta) and Leptolyngbya sp. (Cyanobacteria)] displayed enhanced growth when compared to a Chlorella monoculture; however, the biological mechanisms driving such improvement are currently not well understood. To investigate these mechanisms, this study examined the differential gene expression in the Chlorella between the co-culture and the monoculture. Suppression subtractive hybridization was performed between mRNA from Chlorella in the co-culture and in a monoculture, and 105 genes were identified as being putatively differentially expressed. Nine of these genes, corresponding to the key functional categories of energy, metabolism, and protein synthesis, were further examined using quantitative real-time PCR and showed differential regulation of photosystem I and photosystem II and upregulation of stress-response genes and a gene encoding an oil-globule-associated gene in the co-culture Chlorella. This differential gene expression study of a Chlorella/cyanobacteria co-culture will aid in the development of culture strategies capable of taking advantage of these differences for the production of biomass and bioproducts of interest. Knowledge of the underlying genetic causes of the changes in growth and productivity of the species in co-culture provides insights on possible target genes for optimization of the culture. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication Source (Journal or Book title)
Engineering in Life Sciences
First Page
185
Last Page
193
Recommended Citation
Tate, J., Gutierrez-Wing, M., Rusch, K., & Benton, M. (2013). Gene expression analysis of a Louisiana native Chlorella vulgaris (Chlorophyta)/Leptolyngbya sp. (Cyanobacteria) co-culture using suppression subtractive hybridization. Engineering in Life Sciences, 13 (2), 185-193. https://doi.org/10.1002/elsc.201200063