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Gene expression analysis of a L ouisiana native C hlorella vulgaris ( C hlorophyta)/ Leptolyngbya sp. ( C yanobacteria) co‐culture using suppression subtractive hybridization
Author(s) -
Tate John J.,
GutierrezWing M. Teresa,
Rusch Kelly A.,
Benton Michael G.
Publication year - 2013
Publication title -
engineering in life sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.547
H-Index - 57
eISSN - 1618-2863
pISSN - 1618-0240
DOI - 10.1002/elsc.201200063
Subject(s) - suppression subtractive hybridization , monoculture , gene , biology , gene expression , microbiology and biotechnology , genetics , cdna library , agronomy
A locally isolated co‐culture of two photosynthetic species [ C hlorella vulgaris ( C hlorophyta) and L eptolyngbya sp. ( C yanobacteria)] displayed enhanced growth when compared to a C hlorella 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 C hlorella between the co‐culture and the monoculture. Suppression subtractive hybridization was performed between m RNA from C hlorella 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 C hlorella . This differential gene expression study of a C hlorella /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.

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