Swimming in Light: A Large-Scale Computational Analysis of the Metabolism of Dinoroseobacter shibae
Author(s) -
René Rex,
Nelli Bill,
Kerstin SchmidtHohagen,
Dietmar Schomburg
Publication year - 2013
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1003224
Subject(s) - dimethyl sulfide , flux balance analysis , dimethylsulfoniopropionate , biology , mutant , flux (metallurgy) , gene , chemistry , biochemistry , ecology , nutrient , sulfur , organic chemistry , phytoplankton
The Roseobacter clade is a ubiquitous group of marine α - proteobacteria . To gain insight into the versatile metabolism of this clade, we took a constraint-based approach and created a genome-scale metabolic model ( i Dsh827) of Dinoroseobacter shibae DFL12T. Our model is the first accounting for the energy demand of motility, the light-driven ATP generation and experimentally determined specific biomass composition. To cover a large variety of environmental conditions, as well as plasmid and single gene knock-out mutants, we simulated 391,560 different physiological states using flux balance analysis. We analyzed our results with regard to energy metabolism, validated them experimentally, and revealed a pronounced metabolic response to the availability of light. Furthermore, we introduced the energy demand of motility as an important parameter in genome-scale metabolic models. The results of our simulations also gave insight into the changing usage of the two degradation routes for dimethylsulfoniopropionate, an abundant compound in the ocean. A side product of dimethylsulfoniopropionate degradation is dimethyl sulfide, which seeds cloud formation and thus enhances the reflection of sunlight. By our exhaustive simulations, we were able to identify single-gene knock-out mutants, which show an increased production of dimethyl sulfide. In addition to the single-gene knock-out simulations we studied the effect of plasmid loss on the metabolism. Moreover, we explored the possible use of a functioning phosphofructokinase for D. shibae .
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