Improving the efficiency of enzymes towards decomposing substrates has been one of the central goals in the biotechnology industry. However, the modification of enzymes for upgrading natural materials to high-value performant materials is largely unexplored. Here, we demonstrate that the ancestral form of a Cel5A bacterial endoglucanase, unlike its modern descendant from Bacillus subtilis, was able to generate cellulose nanocrystals (EnCNC) chemically pure, maintaining native cellulose structure and displaying higher thermal stability and crystallinity than standard CNC obtained by acidic treatment. We demonstrate that EnCNC alone is a suitable matrix to grow cells in 2D and 3D cultures. Importantly, EnCNC accepts well graphene derivatives to fabricate conductive hybrids inks forming a stable flat surface where cells also attach and proliferate. Our results demonstrate that EnCNC has physicochemical properties unattainable with standard CNC, making it a unique material ideal as a matrix for the design of biocompatible advanced materials for tissue engineering and other applications.

Clathrate hydrates are crystalline materials made of water molecules forming host cages within which guest molecules are located. The hydrogen bond network ensuring the stability of the host substructure includes ionic defects, having an impact on the physicochemical properties of the systems. In this paper, a new way of introducing these ionic defects is proposed. Type II clathrate hydrates mixing tetrahydrofuran (THF) and perchloric acid guest molecules are synthesized and investigated by means of calorimetric, X-ray diffraction, and Raman scattering measurements together with a computational structure relaxation in the density functional theory approximation. The formation of the mixed clathrate hydrate with perchlorate anion included in the large cage of the cationic host-substructure of the THF type II clathrate hydrate requires the cooling of a (1-α) THF·αHClO4·17H2O solution with α less than 0.125. Above this inherent limitation, a multiphasic regime is observed in the formation of clathrate hydrate (mixture of type I and type II). The substitution of a THF molecule per perchlorate anion allows the modification of the melting of the type II clathrate hydrate, by preserving the clathrate structure. Shrinkage of the type II unit cell is measured together with a softening of the host lattice mode. In the harmonic approximation, the observation of both phenomena is counterintuitive and outline existing competition between anharmonicity of the cage energy landscape and ionic host–guest interaction. This study reveals the key role played by acidic defects existing in the host substructure on the physicochemical properties of clathrate hydrate.

Cellulases catalyze the hydrolysis of cellulose. Improving their catalytic efficiency is a longstanding goal in biotechnology given the interest in lignocellulosic biomass decomposition. Although methods based on sequence alteration exist, improving cellulases is still a challenge. Here we show that Ancestral Sequence Reconstruction can "resurrect" efficient cellulases. This technique reconstructs enzymes from extinct organisms that lived in the harsh environments of ancient Earth. We obtain ancestral bacterial endoglucanases from the late Archean eon that efficiently work in a broad range of temperatures (30-90°C), pH values (4-10). The oldest enzyme (~2800 million years) processes different lignocellulosic substrates, showing processive activity and doubling the activity of modern enzymes in some conditions. We solve its crystal structure to 1.45 Å which, together with molecular dynamics simulations, uncovers key features underlying its activity. This ancestral endoglucanase shows good synergy in combination with other lignocellulosic enzymes as well as when integrated into a bacterial cellulosome.

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Silicon-based polymers show great promise for various applications in biomedicine, nanotechnology, tissue targeting, and drug delivery. The use of such materials as functional coatings on surfaces requires the development of strongly adhering and flexible conformal films, which is challenging for conventional wet-chemical coating techniques. We have developed a facile, solvent-free molecular layer deposition (MLD) process to grow environmentally stable hybrid alumosilazane thin films. Exceptionally good biocompatibility is testified with significantly higher proliferation of human embryonic kidney (HEK293T) cells than that on glass, which was used as a reference. Such highly biocompatible and conformal films show great promise as functional coatings for scaffolds or implantable devices with complex topologies or high-aspect-ratio structures.