Of the two natural metabolic pathways for making terpenoids， biotechnological utilization of the mevalonate (MVA) pathway has enabled commercial production of valuable compounds， while the more recently discovered but stoichiometrically more efficient methylerythritol phosphate (MEP) pathway is underdeveloped. We conducted a study on the overexpression of each enzyme in the MEP pathway in the unicellular cyanobacterium Synechocystis sp. PCC 6803， to identify potential targets for increasing flux towards terpenoid production， using isoprene as a reporter molecule. Results showed that the enzymes Ipi， Dxs and IspD had the biggest impact on isoprene production. By combining and creating operons out of those genes， isoprene production was increased 2-fold compared to the base strain. A genome-scale model was used to identify targets upstream of the MEP pathway that could redirect flux towards terpenoids. A total of ten reactions from the Calvin-Benson-Bassham cycle， lower glycolysis and co-factor synthesis pathways were probed for their effect on isoprene synthesis by co-expressing them with the MEP enzymes， resulting in a 60% increase in production from the best strain. Lastly， we studied two isoprene synthases with the highest reported catalytic rates. Only by expressing them together with Dxs and Ipi could we get stable strains that produced 2.8 mg/g isoprene per dry cell weight， a 40-fold improvement compared to the initial strain.