Biological signaling systems not only detect the absolute levels of the signals, but are also able to sense the fold-changes of the signals. The ability to detect fold-changes provides a powerful tool for biological organisms to adapt to the changes in environment. Here we present the first novel synthetic fold-change detector (FCD) circuit built from ground up in vivo. We systematically designed the FCD circuit in silico, prototyped it in cell-free transcription-translation platform (TX-TL), and eventually implemented it in E. coli cells. We were able to show that the FCD circuit can not only generate pulse-like behavior in response to input, but also produce the same pulse response with inputs of the same fold-change, despite of different absolute signal levels
In this paper, we continue the study on toroidal vertex algebras initiated in
\cite{LTW}, to study concrete toroidal vertex algebras associated to toroidal
Lie algebra Lr(g^)=g^⊗Lr, where
g^ is an untwisted affine Lie algebra and
Lr=\mathbb{C}[t_{1}^{\pm 1},\ldots,t_{r}^{\pm 1}].Wefirstconstructan(r+1)−toroidalvertexalgebraV(T,0)andshowthatthecategoryofrestrictedL_{r}(\hat{\frak{g}})−modulesiscanonicallyisomorphictothatofV(T,0)−modules.Letcdenotethestandardcentralelementof\hat{\frak{g}}andsetS_c=U(L_r(\mathbb{C}c)).WefurthermorestudyadistinguishedsubalgebraofV(T,0),denotedbyV(S_c,0).Weshowthat(graded)simplequotienttoroidalvertexalgebrasofV(S_c,0)areparametrizedbya\mathbb{Z}^r−gradedringhomomorphism\psi:S_c\rightarrow
L_rsuchthatIm\psiisa\mathbb{Z}^r−gradedsimpleS_c−module.DenotebyL(\psi,0}thesimple(r+1)−toroidalvertexalgebraofV(S_c,0)associatedto\psi.Wedetermineforwhich\psi,L(\psi,0)isanintegrableL_{r}(\hat{\frak{g}})−moduleandwethenclassifyirreducibleL(\psi,0)−modulesforsucha\psi$. For our need, we also obtain various
general results.Comment: 50 page