Optimization of Enzymatic Biochemical Logic for Noise Reduction and Scalability: How Many Biocomputing Gates Can Be Interconnected in a Circuit?

We report an experimental evaluation of the "input-output surface" for a biochemical AND gate. The obtained data are modeled within the rate-equation approach, with the aim to map out the gate function and cast it in the language of logic variables appropriate for analysis of Boolean logic for scalability. In order to minimize "analog" noise, we consider a theoretical approach for determining an optimal set for the process parameters to minimize "analog" noise amplification for gate concatenation. We establish that under optimized conditions, presently studied biochemical gates can be concatenated for up to order 10 processing steps. Beyond that, new paradigms for avoiding noise build-up will have to be developed. We offer a general discussion of the ideas and possible future challenges for both experimental and theoretical research for advancing scalable biochemical computing

A n-Bit Reconfigurable Scalar Quantiser

A reconfigurable scalar quantiser capable of accepting n-bit input data is presented. The data length n can be varied in the range 1... N-1 under partial-run time reconfiguration, p-RTR. Issues as improvement in throughput using this reconfigurable quantiser of p-RTR against RTR for data of variable length are considered. The quantiser design referred to as the priority quantiser PQ is then compared against a direct design of the quantiser DIQ. It is then evaluated that for practical quantiser sizes, PQ shows better area usage when both are targeted onto the same FPGA. Other benefits are also identified