Revision as of 09:02, 17 September 2013

lux pL controlled luxR with lux pR controlled ndh (LVA-tag) coding for NADH dehydrogenase II

Description

This part contains two subparts, gfp producer and luxI producer. lux pL promoter, RBS of 1.0 strength, GFP(lva) producer and double terminator. GFP(lva) will be produced after arabinose added. We use this part in our 0,1 dispaly system.

Usage and Biology

The global synchronization mechanism is comprised of two modes of communication that work on different scales. The quorum-sensing machinery (LuxI, AiiA) uses an acyl-homoserine lactone (AHL) to mediate intracolony synchronization. In our device, the degree to which neighbouring colonies are able to influence each other via AHL diffusion is negligible owing to the high media channel flow rates. Instead, we engineered the cells to communicate via gas exchange by placing a copy of the gene coding for NADH dehydrogenase II (ndh) under the control of an additional lux promoter. NDH-2 is a membrane-bound respiratory enzyme that produces low levels of H2O2 and superoxide. As H2O2 vapour is able to pass through the 25-mm oxygen-permeable polydimethylsiloxane (PDMS) walls that separate adjacent colonies, periodic production of NDH-2 yields periodic exchange of H2O2 between biopixels. When H2O2 enters the cell, it transiently changes its redox state, interacting with our synthetic circuit through the native aerobic response control systems, including ArcAB, which has a binding site in the lux promoter region. Under normal conditions, ArcAB is partially active so lux is partially repressed. In contrast, oxidizing conditions triggered by H2O2 inactivate ArcAB, relieving this repression. Each oscillatory burst promotes firing in neighbouring colonies by relieving repression on the lux promoter. This constitutes an additional positive feedback that rapidly synchronizes the population.

We investigated the effects of catalase and superoxide dismutase (SOD) to probe the nature of H2O2 communication. When a population of synchronized colonies was exposed to a step increase of 200Uml21 catalase, an enzyme that rapidly degrades extracellular H2O2, synchronization was broken and colonies continued to oscillate individually (Supplementary Fig. 3). As the cell membrane is impermeable to catalase, asynchronous colony oscillations confirm that communication between colonies depends on external H2O2 whereas oscillations within a colony do not. Conversely, when we enhanced the rate of superoxide conversion to H2O2 by expressing sodA from an additional lux promoter, colonies quickly fired in a spatial wave and failed to oscillate further despite no changes to growth rate or cell viability. BecauseH2O2 is produced internal to the cell, this confirms that H2O2 is capable of escaping the cell and activating lux-regulated genes in neighbouring colonies via diffusion. The apparent higher output ofH2O2 bySODas compared to NDH-2 is probably due to its very high catalytic efficiency. Lastly, we observed synchronization between arrays of traps even when they were fluidically isolated but held in close proximity. These devices share no common fluid sources or channels, making communication by dissolved molecules like AHL impossible. Taken together, these results confirm that gaseousH2O2 is the mode of communication between oscillating colonies.

Protocol

Ndh with LVA tag is formed as a composite by the ligation of quorum sensing promoter luxR via digestion and ligation.

Experimental Data

SDS page, microfluid, and gel image of construction.

Sequence and Features