## Introduction

Cellulose and chitin are the first and second most abundant polymers on the surface of the Earth1, and consequently a recurrent topic of research for their potential utilization in manufacture2,3. Typically, cellulose is associated with plants and chitin with arthropods, however the natural occurrence of both biopolymers as structural components broadens to most kingdoms of eukaryota and bacteria1. Despite their abundance, they rarely coappear in the same organism. One exception of this are certain species of oomycetes4, a large class of eukaryotic organisms. Oomycetes grow in a mycelial form as fungi. However, in contrast to fungi which are characterized by a chitinous wall, oomycetes’ cell walls, and those of their close relative hyphochytrids, are predominately based on cellulose4,5.

In the last few years, the pathogenic nature of some oomycetes has motivated a meticulous characterization of their wall singularities, as possible targets for disease control6. Those studies have also shed some light on the characteristics of natural structures made of chitin and cellulose. This knowledge has direct application on the development of bioinspired materials. We now know oomycetes are not a homogeneous population but a combination of members with at least three distinctive cell wall types7. While those walls are mostly composed of cellulose, they also contain low concentrations of chitinous polymers, comprising up to a 10% of the cellulose content8. Inspired by this idea we studied the effects on manufacturability of cellulose by the addition of small amounts (<15%) of highly deacetylated chitin (i.e. chitosan) and the influence of the chitinous polymer in the ability of the composite to form three-dimensional structures.

The objective of our research is to apply the principles of the cell wall of fungi and oomycetes to produce a general manufacture system based on three premises: (i) The resulting bioinspired composite must be made by its natural constituents; (ii) Components must be available and abundant in every habitat on earth; (iii) Cost, environmental impact, and scalability must enable generalized use. Due to recent research on the oomycetal walls we know that chitin and cellulose produce structural composites in their natural form6, without being regenerated, and therefore our criteria (i) and (ii) are theoretically possible. Additionally, both molecules are common industrial byproducts with a combined cost in the range of commodity plastic9,10,11,12, being exceptional, and probably unique, biological candidates to fulfill criterion (iii).

Our research focuses on the reproduction of the synergies between molecules in biological composites, and we approach this by artificially associating structural biomolecules in their organization in living systems13. This differs from the two predominant approaches to bioinspired materials, based on the reproduction of natural composites with synthetic materials of known manufacturability, and from transforming natural components to fit in already existing manufacture techniques14. The later, has given rise to cellulose modified to form thermoplastic polymers (celluloid), and regenerated to form films (cellophane) or fibers (rayon). These chemical transformations and dissolutions require strong organic solvents and hazardous pollutants such as acetone, carbon disulfide, and sulfuric acid15. As a result, while some of those variants of cellulose were very popular in the 1970′s, their current use has declined to small niche markets16.

In contrast with the chemical stability of cellulose, chitin with low degree of acetylation (i.e. chitosan) contains enough protonatable groups to enable its dispersion in low concentrations (i.e. 1% v/v) of acetic acid17 (e.g. table vinegar 4–10%). Chitosan in solution is driven into a liquid crystal by partial removal of the intermolecular water18 and in that state we used it as external phase to form colloidal dispersions of cellulose fibers. Further removal of the water molecules results in full crystallization of the chitinous polymer and formation of a solid chitosan-cellulose composite (Fig. 1a). Scanning Electron images reveals the original microscopic fibrous structure of the cellulose in the composite (Fig. 1b), while X-Ray diffraction confirms that the cellulose I crystal conformation19 is intact (Fig. 1c). The FTIR spectra of the chitosan and cellulose composites reveals the predominant interaction between the amino and hydroxyl groups respectively3,20 (Fig. 1d). Separate phases of the two components are observed at large concentration of chitosan, turning into a homogenous composite, without phase separation, but with a single decomposition temperature when the concentration of chitosan is under 30% of the total weight (Supplementary Fig. 1).

We further explored the manufacturability of the chitin-cellulose fungus-like material by evaluating the effect of the chitin concentration on the ability of the composite to reach a pliable state and retain shape. Chitosan is introduced in the composite as a water solution. As a result, composites with large amounts of chitosan (>12%) require removal of part of that water until the material reaches a state able to conform and retain a three-dimensional shape (Fig. 2b). After solidification, composites with low amounts of chitosan (<8%) show slender mechanical properties, attributable to its inability to fully bind the cellulose fibers. In contrast, high amounts of chitosan (>17%) produce strong internal forces as the polymers loses water and shrinks, undermining the integrity of structure (Fig. 2c). An inherent optimal ratio of 1:8(w/w) chitosan:cellulose, produces a pliable composite, where no removal of water is required, with minimum shrinking and an unexpected low water uptake (Supplementary Fig. 2). Interestingly, recent studies on the oomycete wall draw similar conclusions for the ratios of chitin/cellulose7, and also reported an abnormal water uptake on the cell wall when chitin production is disrupted6. The fungus-like additive material (FLAM) has a cost of about 2 $/kg and, with a young modulus of 0.26 Gpa and a density of 0.37 g/cm3. It is wort noting that while the cost of FLAM is in the range of commodity plastics, is more than ten times lower than those of common filaments for 3D printing, such as PLA and ABS with an average cost of 20–30$/kg. The mechanical characteristics of FLAM are within the range of natural cellulosic composites such as medium to low density woods and high-density foams, commonly used in product design, construction, aviation and automotive industries (Fig. 2a,d, Supplementary Fig. 3, Supplementary Table 2, and Supplementary Movie 1). Nevertheless, they are significantly different to any characterized natural material. FLAM is a reproduction of a natural material synthesized at the microscale (i.e. the oomycete wall), so it is probable its characteristics are similar to uncharacterized materials existing only at that scale. The only reported material with almost identical mechanical characteristics to FLAM is high-ending rigid polyurethane foam (i.e. pcf-30), commonly used for production of synthetic bones21.

While most cellulosic and chitinous natural structures also include other organic and inorganic components, the interaction between cellulose and chitosan has proven sufficient to form solid composites. These interactions are strong enough even in presence of disruptive components, such as lignin or hemicellulose, enabling the formation of wood flour-based composites (Fig. 3a). The mechanical characteristics of these wood-based composites are significantly lower than FLAM based on pure cellulose (Supplementary Table 2), yet they enable a generalization of the technology to many other sources of unprocessed byproducts. In the US for example, 14% of the municipal waste is wood22, while industries such as agriculture, food, textile, and paper, produce high amount of waste with high cellulose content. We tested wood flour from three different sources and purities, producing composites and objects with small mechanical differences with respect to the waste source or the manufacture method (Fig. 3b, Supplementary Fig. 3, and Supplementary Table 2). This chitinous property of binding cellulosic composites is retained by FLAM as when FLAM is deposited on wood it naturally forms adhesion bonds able to hold an average of 33.5 ± 7.3 kg per cm2 (Fig. 3a). This feature broadens the applicability of the material to an unprecedented range of strategies: it can be machined using common woodworking techniques such as sawing and sanding, (Fig. 3c and Supplementary Movie 2) as well as used in combination with hardwood and other cellulosic components (Fig. 3c, Supplementary Fig. 4, and Supplementary Movie 3). More interestingly, the property of FLAM to bond with cellulosic composites also include fusing with itself, enabling its use in additive manufacturing (Supplementary Fig. 3).

No technology has ever been reported to possess the unique characteristics of FLAM: made of the two most abundant and broadly distributed components on earth, lightweight, cost in the range of commodity plastics, suitable for large-scale manufacture, lack of harmful solvents/pollutants, compatible with cellulosic composites, completely biodegradable out of composting systems. Additionally, to our knowledge, there is no other biotic material with the adaptability to be casted, molded, sanded, sawn and 3D printed. It is expected that FLAM can delocalize general manufacture and meet the emerging needs of sustainable manufacture, large-scale fabrication, and circular economy, as well as be a disruptive technology across multiple industries, including the architectural, aerospace, and biomedical, enabling the development of many more areas and new manufacture strategies beyond the current reach of technology.

## Materials and Methods

### Materials

High Purity cellulose (JELUCEL® HM400X; fiber size <200 μm) and wood flour- W1 (JELUXYL® WEHO 500; grain size <500 μm) were supplied by JELU-WERK GmbH & Co. KG, Germany. Sawdust- byproducts of the woodwork machines was collected from fabrication lab-SUTD (W2), Singapore. Chitosan used in the manufacturing process was purchased from i-CHESS chemicals Pvt Ltd., India (Table S1). Chitosan (medium molecular weight; 75–85% deacetylated) used for molecular characterization and glacial acetic acid, were purchased from Sigma-Aldrich, Singapore. All chemicals were used as received. FLAM preparation: Chitosan solution (3% w/w) was prepared by dissolving chitosan in 1%(v/v) acetic acid. Fungus-like additive materials (FLAM) were prepared by mixing chitosan solution and cellulose (C:C) in varying ratio (dry w/w) 1:1, 1:2, 1:4, 1:6, 1:8 and 1:10, and were used to cast films for molecular characterization, specimens for mechanical characterization and hand-casted structures followed by oven drying at 50 °C. The FLAM to manufacture macrostructures were prepared in a 1:8 ratio (C:C) by mixing in an Industrial dough mixer (B25-25L, Yiwu Sneeceman, China) and 90 rpm.

### Molecular Characterization and imaging

Scanning electron microscopy: The surface morphology of FLAM films was examined using a Field Emission Scanning Electron Microscope (FESEM, JEOL, JSM-7600F) at 5 kV accelerating voltage. Samples were mounted onto a carbon tape on an aluminum stub and sputter coated with gold for 30 s. X-ray diffractionmetry: X-ray diffraction diagrams of cellulose and composite films were obtained on a X-ray Diffraction System (XRD)- D8 Discover Bruker, using nickel-filtered CuKα radiation (λ = 0.15418 nm) operated at 40 mA and 40 kV, with a scan speed of 3°/min having set the 2θ angle 2° to 60°. FTIR: FTIR spectra of composite films were obtained using a Fourier transform infrared (FTIR) spectrometer, VERTEX 70 FTIR (Bruker optik GmbH), with a resolution of 4 cm−1 and accumulation of 32 scans between 4000 to 400 cm−1 on ATR mode. TGA: Thermogravimetric analysis (TGA) of samples were carried out on a Thermogravimetric Analyzer TA Q50, TA instruments, using a temperature ramp from 30 °C to 700 °C at a heating rate of 10 °C/min in a nitrogen atmosphere. Rheological measurements: The flow behaviors of FLAMs were determined by measuring the dynamic shear viscosity with different shear rates (0.05–30 s−1) on a Rheometer (HR-2 Discovery Hybrid Rheometer, TA instruments equipped with Environmental Test Chamber), using parallel plate geometry (40 mm diameter; 500 μm gap). FLAMs with ratio 1:2, 1:4 and 1:6 were kept in an oven at 50 °C with frequent stirring and viscosity of each sample was measured periodically at 0, 2, 4, 6, 8, 10, 12, 16, 20, 24, 27 and 30 h, until viscosity reached to the pliable range. Prepared pliable composites were further used for tensile strength and shrinking behavior measurements.

### Moisture absorption measurement

Moisture absorption measurement was carried on completely dried and pre-weighed mold-casted cuboids with the size 30 × 15 × 15 mm. The samples were placed in the humidity chamber at 95% humidity at 25 °C for certain time.

The moisture absorption (%) was calculated using the following equation (1)

$${Moisture}\,{absorption}\,( \% )=\frac{{{M}}_{{w}}-{{M}}_{{d}}}{{{M}}_{{d}}}\times 100$$
(1)

Here, Md is the weight of the dry specimen before placing in humidity chamber and Mw is the weight after moisture absorption at certain time.