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Michael J. Federle, Bonnie L. Bassler
Published in Volume 112, Issue 9
J Clin Invest. 2003; 112(9):1291–1299 doi:10.1172/JCI20195
Abstract | Full text | PDF
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Figure 4

Biosynthesis of AI-2. Utilization of SAM as a methyl donor in cellular processes yields S-adenosylhomocysteine (SAH). The enzyme Pfs converts SAH to S-ribosylhomocysteine (SRH). LuxS is responsible for the conversion of SRH to homocysteine and DPD. DPD is predicted to spontaneously rearrange into various furanones. The furanone predicted to lead to the formation of V. harveyi AI-2 is the only one shown and is termed pro–AI-2. Borate adds to pro–AI-2 to form the active signaling molecule AI-2.