Superabsorbent bacterial cellulose spheres biosynthesized from winery by-products as natural carriers for fertilizers.

Soil contamination, sustainable management of water resources and controlled release of agrochemicals are the main challenges of modern agriculture. In this work, the synthesis of sphere-like bacterial cellulose (BC) using agitated culture conditions and Komagateibacter medellinensis bacterial strain ID13488 was optimized and characterized from grape pomace (GP). First, a comparative study was carried out between agitated and static cultures using different nitrogen sources and applying alternative GP treatments. Agitation of the cultures resulted in higher BC production yield compared to static culture conditions. Additionally, Water holding capacity (WHC) assays evidenced the superabsorbent nature of the BC biopolymer, being positively influenced by the spherical shape as it was observed an increase of 60% in contrast to the results obtained for the BC membranes under static culture conditions. Moreover, it was found that sphere-like BCs were capable of retaining urea up to 375% of their dry weight, rapidly releasing the fertilizer in the presence of water. According to our findings, sphere-like BCs represent suitable systems with great potential for actual agricultural hazards and grape pomace valorisation.

Tailoring the in situ conformation of bacterial cellulose-graphene oxide spherical nanocarriers.

Bacterial cellulose (BC)/graphene oxide (GO) sphere-like hydrogels have been biosynthesized by in situ route in dynamic cultivation. The GO concentration during BC biosynthesis (0.01 and 0.05 mg mL-1) was the determining factor for the conformation of the final hydrogels: encapsulation (BC/GO 0.01) or distribution through all the body of the spheres (BC/GO 0.05). The as-prepared sphere hydrogels were characterized in terms of physico-chemical properties, thermal stability, microstructure, and swelling capacity in different media. In addition, a chemical treatment with ascorbic acid was performed in order to obtain reduced graphene oxide (rGO) into the spheres (BC/rGO). After the chemical treatment, electrostatic force microscopy (EFM) revealed electrical interactions due to the presence of rGO inside the spheres and resistivity values in the range of semiconductive materials were obtained (106 Ω·cm), making BC/rGO spheres promising for the development of electro-stimulated systems. The in vitro release study of ibuprofen (IB), showed that the reduction process led to an increase of 73 and 92% of drug release with respect to BC/GO 0.05 and BC/GO 0.01 spheres, respectively. Moreover, the encapsulation conformation showed more homogeneous porous structure and thus, a cumulative drug release of 63% was reached after 6 h.

Hybrid and biocompatible cellulose/polyurethane nanocomposites with water-activated shape memory properties.

Water-activated shape memory bacterial cellulose/polyurethane nanocomposites were prepared by the immersion of bacterial cellulose (BC) wet membranes into waterborne polyurethane (WBPU) dispersions for different times. The high affinity between the hydrophilic BC and water stable polyurethane led to the coating and embedding of the BC membrane into the WBPU, facts that were confirmed by FTIR, SEM and mechanical testing of the nanocomposites. The mechanical performance of the nanocomposites resulted enhanced with respect to the neat WBPU, confirming the reinforcing effect of the BC membrane. An improvement of the shape fixity ability and faster recovery process with the presence of BC was observed. In 3 min, the nanocomposite with highest BC content recovered the 92.8 ± 6.3% of the original shape, while the neat WBPU only recovered the 33.4 ± 9.6%. The obtained results indicated that 5 min of impregnation time was enough to obtain nanocomposites with improved mechanical performance and fast shape recovery for potential biomedical applications. The present work provides an approach for developing environmentally friendly and biocompatible BC/polyurethane based materials with enhanced mechanical and shape memory properties.

Bacterial nanocellulose production from naphthalene.

Polycyclic aromatic compounds (PAHs) are toxic compounds that are released in the environment as a consequence of industrial activities. The restoration of PAH-polluted sites considers the use of bacteria capable of degrading aromatic compounds to carbon dioxide and water. Here we characterize a new Xanthobacteraceae strain, Starkeya sp. strain N1B, previously isolated during enrichment under microaerophilic conditions, which is capable of using naphthalene crystals as the sole carbon source. The strain produced a structured biofilm when grown on naphthalene crystals, which had the shape of a half-sphere organized over the crystal. Scanning electron microscopy (SEM) and GC-MS analysis indicated that the biofilm was essentially made of cellulose, composed of several micron-long nanofibrils of 60 nm diameter. A cellulosic biofilm was also formed when the cells grew with glucose as the carbon source. Fourier transformed infrared spectroscopy (FTIR) confirmed that the polymer was type I cellulose in both cases, although the crystallinity of the material greatly depended on the carbon source used for growth. Using genome mining and mutant analysis, we identified the genetic complements required for the transformation of naphthalene into cellulose, which seemed to have been successively acquired through horizontal gene transfer. The capacity to develop the biofilm around the crystal was found to be dispensable for growth when naphthalene was used as the carbon source, suggesting that the function of this structure is more intricate than initially thought. This is the first example of the use of toxic aromatic hydrocarbons as the carbon source for bacterial cellulose production. Application of this capacity would allow the remediation of a PAH into such a value-added polymer with multiple biotechnological usages.

Genome sequence and characterization of the bcs clusters for the production of nanocellulose from the low pH resistant strain Komagataeibacter medellinensis ID13488.

Komagataeibacter medellinensis ID13488 (formerly Gluconacetobacter medellinensis ID13488) is able to produce crystalline bacterial cellulose (BC) under high acidic growth conditions. These abilities make this strain desirable for industrial BC production from acidic residues (e.g. wastes generated from cider production). To explore the molecular bases of the BC biosynthesis in this bacterium, the genome has been sequenced revealing a sequence of 3.4 Mb containing three putative plasmids of 38.1 kb (pKM01), 4.3 kb (pKM02) and 3.3 Kb (pKM03). Genome comparison analyses of K. medellinensis ID13488 with other cellulose-producing related strains resulted in the identification of the bcs genes involved in the cellulose biosynthesis. Genes arrangement and composition of four bcs clusters (bcs1, bcs2, bcs3 and bcs4) was studied by RT-PCR, and their organization in four operons transcribed as four independent polycistronic mRNAs was determined. qRT-PCR experiments demonstrated that mostly bcs1 and bcs4 are expressed under BC production conditions, suggesting that these operons direct the synthesis of BC. Genomic differences with the close related strain K. medellinensis NBRC 3288 unable to produce BC were also described and discussed.

Design of reusable novel membranes based on bacterial cellulose and chitosan for the filtration of copper in wastewaters.

This study has been carried out to design novel, environmentally friendly membranes by in situ and ex situ routes based on bacterial cellulose (BC) as a template for the chitosan (Ch) as functional entity for the elimination of copper in wastewaters. Two routes led to bionanocomposites with different aspect and physico-chemical properties. The mechanical behaviour in wet state, strongly related to crystallinity and water holding capacity, resulted to be very different depending on the preparation route although the Ch content was very similar: 35 and 37 wt% for the in situ and ex situ membranes, respectively. The morphological characterization suggested a better incorporation of the Ch into BC matrix through the in situ route. The cooper removal capacity of these membranes was analyzed and in situ prepared membrane showed the highest values, about 50%, for initial concentrations of 50 and 250 mg L-1. Moreover the reusability of the membranes was assessed. This is the first time that the whole 3D nano-network BC membrane is used to provide physical integrity for chitosan to develop eco-friendly membranes with potential applications in heavy metal removal.