Model-structure identification is important for the optimization and design of biokinetic processes. Standard Monod and Tessier functions are often used by default to describe bacterial growth with respect to a substrate, leading to significant optimization errors in case of inappropriate representation. This paper introduces shape-constrained spline (SCS) functions, which share the qualitative behavior of a number of conventional growth-rate functions expressing substrate affinity effects. A simulated case study demonstrates the capabilities in terms of model identification of SCS functions, which offer a high parametric flexibility and could replace incomplete libraries of functions by a single biokinetic model structure. Moreover, the diagnostic ability of the spline functions is illustrated for the case of Haldane kinetics, which exhibits a distinctively different shape. The major benefit of these spline functions lies in their model discrimination capabilities by indicating in a quick and conclusive way the presence of other effects than substrate affinity.
Rakesh Chawla, Andrea Rizzi, Matthias Finger, Federica Legger, Matteo Galli, Sun Hee Kim, Jian Zhao, João Miguel das Neves Duarte, Tagir Aushev, Hua Zhang, Alexis Kalogeropoulos, Yixing Chen, Tian Cheng, Ioannis Papadopoulos, Gabriele Grosso, Valérie Scheurer, Meng Xiao, Qian Wang, Michele Bianco, Varun Sharma, Joao Varela, Sourav Sen, Ashish Sharma, Seungkyu Ha, David Vannerom, Csaba Hajdu, Sanjeev Kumar, Sebastiana Gianì, Kun Shi, Abhisek Datta, Siyuan Wang, Anton Petrov, Jian Wang, Yi Zhang, Muhammad Ansar Iqbal, Yong Yang, Xin Sun, Muhammad Ahmad, Donghyun Kim, Matthias Wolf, Anna Mascellani, Paolo Ronchese, , , , , , , , , , , , , , , , , , , , , , , ,
Michaël Unser, Joaquim Gonçalves Garcia Barreto Campos, Alexis Marie Frederic Goujon