Bioconversion of potato solid waste into antifungals and biopigments using Streptomyces spp.

Potato waste was processed and used as a sole substrate for simultaneously producing antifungals and biopigments using Streptomyces spp. Out of three different Streptomyces isolates, strain SO6 stood out due to its ability to produce antifungals against economically important fungal phytopathogens and intracellular biopigments using potato waste powders without additional nutrients. This strain also showed the potential to secrete a broad range of enzymes for fermentation of eight sugars that could be involved in potato waste bioconversion. The results of the fermentation assay indicated that Streptomyces sp. strain SO6 degrades potato wastes during submerged fermentation, diminishing total dry weight and increasing reducing sugars from 0.3 to 3.6 mg·mL−1 and total proteins from 70.6 to 187.7 μg·mL−1. The results showed that Streptomyces strain SO6 was able to convert the potato waste into 0.96 mg·g−1 of diffusible antifungals and 1.75 mg·g−1 of reddish-purple biopigments. On the contrary, an absence of pigment production was observed during the fermentation of the commercial medium used as reference. According to our results, replacement of commercial culture media with available low-cost agroindustrial wastes for producing bioactive chemicals is a real opportunity to enhance the Streptomyces pigment production and antibiotic sustainability with cost-competitiveness. To our knowledge, this is the first report on the simultaneous production of biopigments and diffusible antifungal antibiotics produced by Streptomyces spp. using potato solid waste as the sole nutrient source.


Introduction
The agri-food sector generates large amounts of wastes that require sustainable eco-friendly alternatives for utilization rather than waste disposal [1]. According to the Food and Agriculture Organization (FAO) [2], one-third of food produced for human consumption is lost every year or wasted throughout the supply chain (~1.3 billion tons). The generated wastes are a rich source of microbial nutrients (e.g., carbohydrates, proteins, minerals, and vitamins) that can a1111111111 a1111111111 a1111111111 a1111111111 a1111111111 peel (e.g., cuts and blemishes). Traditionally, potato waste is used for producing low-value animal feed and fertilizer or used as the raw material of biogas, which leads to waste of abundant nutritive materials [29]. However, the nutrient content of discarded potato makes it an interesting byproduct for obtaining high-value-added products with different biotechnological applications [30], especially since the agro-industrial wastes are considered a key component in the circular bioeconomy [31].
In Chile, a high amount of discarded potato is generated each season according to the Oficina de Estudios y Políticas Agrarias de Chile (ODEPA) [32], which is directly eliminated to avoid decomposition and proliferation of plant diseases or, if possible, sold at a very low price (less than 1 USD per 50 kg bag) for animal feed. An alternative for valorizing this potato waste is its use as a nutritional source for producing antifungals and biopigments by Streptomyces spp., which could offer product diversification for farmers and environmental sustainability (S1 Fig).
Interestingly, a recent study on the use of lignocellulosic materials for the simultaneous production of carbohydrates, lipids, and pigments by the anoxygenic photosynthetic bacteria R. faecalis was reported by Saejung and Sanusan [33]. These studies are a starting point for the further simultaneous production of microbial value-added products using agro-industrial wastes as low-cost nutrient sources for large-scale industrial production. To the best of our knowledge, there are no reports of the use of starch-rich wastes for the simultaneous production of antifungals and biopigments by Streptomyces spp. In this research, we aimed to evaluate the use of potato solid waste as a nutrient source for the simultaneous production of antifungal antibiotics and biopigments by Streptomyces spp. under submerged fermentation.
The culture medium potato dextrose agar (PDA) for fungus maintenance and antifungal assays was purchased from Merck (Darmstadt, Germany). The International Streptomyces Medium No. 2 (ISP2; glucose 4 g, yeast extract 4 g, malt extract 10 g, distilled water 1 L, pH 7.0) was used for propagation of Streptomyces strains. The previous ISP2 broth was jellified with agar-agar granulated (15 g�L −1 ) to prepare ISP2 agar medium. All the ISP2 components were purchased from Merck (Darmstadt, Germany).

Potato waste processing
The potatoes (Solanum tuberosum L.) used in the preparation of culture media were discarded potatoes obtained from a local potato-producing company near Temuco City in Chile. These potatoes were cut into small pieces (1 × 1 cm), dried at 70˚C for 24 h, and ground to a fine powder. The proximate composition of the potato waste powder (PW) was reported in our previous study, as described by Schalchli et al. [34] (moisture 7.8%; fat 6.2%; protein 7.9%; crude fiber 0.4%; ash 3.9; N-free extract 73.7%). In this study, a morphological and semiquantitative determination of the elemental composition of the PW surfaces was carried out by means of a variable pressure scanning electron microscope (VP-SEM, Model SU 3500-Hitachi; Hitachi Corp., Japan) with an X-ray spectroscopy (EDX) detector (Quantax-Bruker). The particle size of PW was between 10 and 200 μm (Fig 1a) and contained different proportions of carbon, oxygen, nitrogen, and potassium (Fig 1b). The PW was used to prepare PW broth (16 g�L −1 ) and PW agar (PW 8 g�L −1 , agar-agar 15 g�L −1 ) without the addition of supplements and pH adjustment [34].

Microbial strains
Three Streptomyces strains with different morphological characteristics and pigmentation were obtained from the strain collection at the Laboratory of Biotechnology, Universidad de La Frontera (Chile). The strains were previously isolated from soil samples and preserved due to their antifungal activity against Mucor miehei(Cooney et Emerson Tü 284). The Streptomyces strains SO6, PM1, and PM7 are conserved in the Chilean Culture Collection CCCT-UFRO with the following codes: CCCT21.05, CCCT21.03, and CCCT 21.04, respectively. For the assays, the bacterial colonies were maintained on ISP2 agar slants and stored at 4˚C. The spore solution of Streptomyces spp. was prepared by flooding agar ISP2 plates with 20 mL of distilled water and used as inoculum at a spore concentration of 10 4 spores�mL −1 . A pre-inoculum for fermentation assay was prepared, consisting of 10 4 spores�mL −1 of Streptomyces sp. SO6 cultured in 200 mL of ISP2 broth and incubated at 28˚C and 120 rpm for 48 h in darkness.
The phytopathogenic fungi B. cinerea (CCCT21.01) and F. oxysporum (CCCT 21.02) were used as target fungi for evaluating the antifungal activity of Streptomyces strains. The fungus M. miehei (Cooney et Emerson Tü 284) was used as a reference strain for detecting antibiotic metabolites. For the assays, all fungal strains were maintained on PDA slants at 4˚C. Before their use, the fungal strains were subcultured from stock slants onto PDA plates and incubated for 5 days at 25 ± 1˚C. A spore solution of B. cinerea was prepared by flooding PDA plates with 20 mL of distilled water and used in disc agar-diffusion testing at a spore concentration of 10 6 spores�mL −1 .

Characterization of Streptomyces spp.
The Streptomyces strains SO6, PM1, and PM7 were characterized in terms of morphological, biochemical, and molecular properties. To determine the morphological characteristics, samples of 5-day old Streptomyces cultures were analyzed using a VP-SEM (Model SU 3500-Hitachi; Hitachi Corp., Japan). For biochemical characterization, we used Api-Coryne test strips (Biomerieux 1 , USA) according to the manufacturer's instructions. The amylase and protease activities were determined following the methodologies described by Minotto et al. [35] and Vaithanomsat et al. [36]. Lastly, the Streptomyces strains were characterized using a genetic affiliation analysis of 16S ribosomal DNA (rDNA) gene fragments from the Streptomyces genus. For this, the F341/R534 primer pair was employed [37]. The 16S rDNA fragments were sequenced in both directions using an automated sequencing system (Macrogen, Korea). Sequences were compared with the Basic Local Alignment Search Tool (BLAST) database.

Evaluation of antifungal activity and biopigment production
The three Streptomyces strains were assayed for potential antifungal activity against the target fungi B. cinerea, F. oxysporum, and M. miehei using a dual culture assay on 90 mm PDA and PW agar (8 g�L −1 PW) plates according to Landa et al. [38], with modifications. Fresh cultures of 5-day old Streptomyces strains were streaked (approximately 4 cm line) on one side of the plate and incubated for 5 days at 28˚C. Then, the plates were inoculated with one mycelial plug (6 mm in diameter) of 5-day old target fungi on the opposite side and incubated until the control plate reached the edge. Three replicate plates were used for each dual culture. The antifungal activity was evaluated by measuring the inhibition zones expressed in mm of inhibition against the target fungi according to Kim et al. [39]. An optical microscope (Euromex IS 1153-EPL model, Holland) was used to facilitate the localization of fungal hyphae and to avoid any subjective measurements of fungal growth inhibition.
The three Streptomyces spp. were cultured in PW broth at a concentration of 16 g�L −1 PW and ISP2 medium. For this, 1 L Erlenmeyer flasks containing 500 mL of each culture medium inoculated with a bacterial suspension of 10 4 spores�mL −1 were incubated at 28˚C and 120 rpm for 10 days on a rotary shaker in darkness. The pigment formation was confirmed by observation of colored cultures. Lastly, the strain able to inhibit all the target fungi and produce biopigments using PW as the sole nutrient source was selected for the batch fermentation assay.

Batch fermentation assay
The batch fermentation assay was performed according to Sharmila et al. [40], with modifications. Briefly, 250 mL Erlenmeyer flasks containing 100 mL of PW broth (16 g�L −1 PW) without pH adjustment (initial pH~6.2) were inoculated with fresh inoculum of Streptomyces sp. SO6 (4% v/v). The flasks were incubated at 28˚C and 120 rpm for 10 days in darkness. Additionally, ISP2 medium was used for comparative purposes and incubated in the same conditions. The control treatment was the same PW broth and ISP2 medium without bacterial inoculum. Each assay was carried out in triplicate under destructive sampling mode. Every 24 h, the pH value using a pH-meter, reducing sugars using the DNS method [41], and total protein [42] were measured. For dry weight determination, the bacterial/PW biomass was separated by filtration and then dried at 105˚C until a constant weight was achieved.

Obtention of crude extracts
Streptomyces sp. strain SO6 was cultured in PW broth medium to obtain EtOAc crude extracts as previously described [40,43]. Two Erlenmeyer flasks (1 L) containing 500 mL of PW broth (16 g�L −1 PW) without pH adjustment (initial pH 6.2) were inoculated with a suspension of 10 4 spores�mL −1 of Streptomyces sp. strain SO6 and incubated at 28 ± 1˚C under agitation (120 rpm). After 2 weeks of fermentation, the culture was separated by vacuum filtration to obtain cell-free supernatant and bacterial/PW biomass.
The cell-free supernatant was extracted exhaustively with EtOAc, filtered in a decanting funnel, concentrated to dryness in a SPD121P SpeedVac 1 Concentrator (Thermo Scientific Savant 1 ), and stored at 4˚C [44]. The biomass was maintained in 200 mL of EtOAc for 1 week at 4˚C to macerate before final extraction. After this, the pigmented EtOAc was filtered, concentrated to dryness, and stored at 4˚C. The ultraviolet/visible light (UV/Vis) absorption spectrum (380-750 nm) of pigmented EtOAc was determined using a Synergy H1 multimode microplate reader (BioTek) before conservation.
The obtained EtOAc crude extracts from cell-free supernatant and biomass were assessed separately for determining their antifungal activity using disc agar-diffusion testing [45] against the plant pathogenic fungus B. cinerea at a concentration of 100 μg�disc −1 . For this, 100 mL of PDA medium was inoculated with B. cinerea (10 6 spores�mL −1 ) and placed in 90 mm Petri dishes. Then, 100 μg of crude EtOAc extract previously solubilized in MeOH was placed on filter paper discs (6 mm in diameter) and deposited on the surface of the B. cinerea plate. After 4 days of incubation at 28˚C, the inhibition zones were measured (mm in diameter).

Isolation and purification of antifungals
The EtOAc crude extracts from cell-free supernatant were analyzed by CC combined with preparative and analytical thin-layer chromatography (TLC) to isolate fractions according to Siddharth and Rai [44], with modifications. For this, the crude EtOAc extract (~330 mg) was loaded onto a silica gel column (30 × 2.5 cm) and eluted with a gradient of solvents Hex/Chl/ EtOAc/MeOH (100% Hex!100% MeOH). The fractions were collected and validated by TLC using silica gel 60 F 254 plates and Hex:EtOAc:MeOH (7:2:1) as the mobile phase. The fractions with the same retention factor (R f ) values, visualized with visible and UV light at 365 and 254 nm, were combined and concentrated to obtain homogeneous fraction groups. Two TLC plates were used in parallel in each experiment. Each fraction group was concentrated to dryness and analyzed for its antifungal activity against B. cinerea using the previously described disc agar-diffusion testing to identify the active fractions.

Isolation and purification of biopigments
The EtOAc crude extract from the biomass was analyzed by CC combined with preparative and analytical TLC to determine its content of biopigments according to Siddharth and Rai [44], with modifications. The EtOAc extract (~58 mg) was loaded onto a silica gel column (30 × 2.5 cm) and eluted with a gradient of Hex/Chl/EtOAc/MeOH (100% Hex!100% MeOH). The fractions (63) were collected and validated by TLC using silica gel 60 F 254 plates and Hex: EtOAc:MeOH (7:2:1) as the mobile phase. The fractions with the same R f values, visualized with visible and UV light at 365 and 254 nm, were combined and concentrated to obtain homogeneous fraction groups. Two TLC plates were used in parallel in each experiment. On the basis of the presence of pigmentation with similar R f values, the fraction groups F3 and F4 were pooled and analyzed by preparative TCL to determine their purity. The preparative TLC was carried out using silica gel 60 F 254 plates and Hex:EtOAc:MeOH (7:2:1) as the mobile phase.

Statistical analysis
Data from the dual culture assay (mm) were averaged, and the standard errors (SD) of the means were calculated. Differences among treatments were assessed with one-way analysis of variance (ANOVA) and post hoc analysis of differences in means was conducted with the Tukey test using JMP 11.0 software (SAS Institute Inc., NC, USA) with statistical significance set at p < 0.05.

Characterization of Streptomyces strains
Differences in terms of the type of branch, colony pigmentation, gelatin hydrolysis, carbohydrate fermentation (glucose, ribose, xylose, and mannitol), and enzymes (N-acetyl-β-glucosaminidase and urease) were found between the active strains. The morphological and biochemical characteristics of the active strains are shown in Table 1. Analysis of the 16S rRNA gene revealed that the PM1, PM7, and SO6 strains show high levels of sequence similarity to Streptomyces spp. accession numbers EU216727 (93%), GU985264 (99%), and HM125709 (99%), respectively.

Antifungal activity and biopigment production by Streptomyces spp.
The Streptomyces strains PM1, PM7, and SO6 were able to produce different culture pigmentations and inhibit the mycelial growth of the reference fungus M. miehei and the plant pathogenic fungus B. cinerea using commercial culture media. F. oxysporum growth was slightly inhibited by the PM1 and SO6 strains, but was not inhibited by PM7 (Table 2). There were significant differences (p � 0.05) among the antifungal activities of the three actives Streptomyces strains against the target fungi using both PDA and agar PW media. Concerning biopigment production, the strains PM7 and SO6 maintained their biopigment production when ISP2 medium was replaced with PW broth (Fig 2).
Although all the tested Streptomyces spp. were able to produce biopigments and inhibit B. cinerea and M. miehei growth using commercial media, the SO6 strain stood out due to its ability to produce antifungals against the three target fungi while maintaining its pigment production in the culture medium formulated with PW. Therefore, Streptomyces sp. strain SO6 was selected for PW fermentation assays and studies on the obtained bioproducts.

Batch fermentation assay
To test the potential use of PW as a nutrient source for producing high-value-added bioproducts by Streptomyces sp. strain SO6, submerged fermentation assays without pH adjustment Table 2

PLOS ONE
and/or supplementation were performed. Fig 3 shows the dry weight of total biomass, pH, and reducing sugar and total protein content in PW broth and ISP2 (control treatment) over the 10 day fermentation assay. As shown in Fig 3a, the dry weight increased during the first 6 days in ISP2 medium (log phase) and then remained constant at~1.2 mg dry wt�mL −1 until the end of the fermentation assay (stationary phase). However, when the same Streptomyces sp. strain SO6 was grown in PW medium, the dry weight (PW and bacterial biomass) did not differ significantly (p < 0.05) from the control treatment (without bacteria) over the fermentation time. The PW broth with or without inoculum showed a higher dry weight than ISP2 treatments due to the particle size and solubility of the culture components. The pH decreased during fermentation of Streptomyces sp. strain SO6 into ISP2 medium from 6.6 to 4.9 (at day 2) and then remained constant until the end of the fermentation assay (Fig 3b). In contrast, the pH of PW medium increased considerably on the second day of incubation (from 5.8 to 8.0), remaining constant from the fifth day (~6.4). In addition to the microbial biomass increase in ISP2 medium, the content of reducing sugars decreased steadily from 9.5 to 6.4 mg�mL −1 at day 10. The initial reducing sugar content in PW medium was 0.6 mg�mL −1 , which increased to a maximum of 3.6 mg�mL −1 on the sixth day of incubation. After the sixth day, reducing sugars consistently decreased until the end of the PW fermentation assay (Fig 3c). The changes in total proteins in both ISP2 and PW media are shown in Fig 3d. The maximum value of total protein content in ISP2 medium with Streptomyces sp. strain SO6 was 47 μg�mL −1 on the fifth day of incubation, remaining constant over time (Fig 3d). Interestingly, total protein secretion was noticeably higher in PW inoculated with Streptomyces sp. strain SO6 compared to the control flask, reaching 179 μg�mL −1 of total proteins on the fifth day of incubation (~3.8-fold increase).
Lastly, pigment formation was observed in PW medium on the fourth day of incubation, whereas there was no pigmentation in ISP2 over the time considered for the fermentation assay (Fig 3e). The UV/Vis spectra revealed a maximum absorption peak (λ max ) at 520 nm. A relationship between the pigment concentration and the PW concentration over time was also observed (result not shown).

Antifungal and biopigment production by Streptomyces sp. strain SO6
An initial analysis of the antifungal activity of the EtOAc extracts from both cell-free supernatant and biomass was performed to identify active extracts. The results showed that antifungal compounds were produced by Streptomyces sp. strain SO6 using PW as a nutrient source and released into the culture medium. Fig 4a shows the mycelial growth inhibition (19 mm in diameter) of the plant pathogen B. cinerea by the cell-free supernatant EtOAc extract at a concentration of 100 μg per disc. In contrast, no inhibition of B. cinerea was observed in the negative control treatment (EtOAc) (Fig 4a).
An absence of the typical orange-red coloration was also observed in the cell-free supernatant after separating it from the biomass. Although the biomass EtOAc extract showed no antifungal activity, a marked orange-red coloration was observed (Fig 4a). From these results, the studies were directed to analyze the antifungal compounds in the cell-free supernatant EtOAc extract, while biopigments were analyzed in the biomass EtOAc extract. For this, the compounds in both the cell-free supernatant and the biomass EtOAc extracts were fractionated separately by means of CC and TLC. Fractions with similar TLC patterns were pooled to give TLC homogeneous groups and determine the yields of antifungals and biopigments.
Among the 15 homogeneous groups of fractions (F1 to F15) from the cell-free supernatant EtOAc extract, two groups showed high antifungal activity against B. cinerea growth (Fig 4b). Groups F7 and F8 (28 mg total yield) showed inhibition halos of 9 ± 1 and 19 ± 3 mm (in diameter), respectively.
A total of 12 homogenous groups were also obtained from the biomass EtOAc extract by combining fractions with identical TLC patterns. Groups F3 and F4 were pooled later due to their identical coloration and Rf values, obtaining a total yield of 15.3 mg of a reddish-purple pigment (Fig 5a). The preparative TLC showed at least three major reddish-purple bands (Fig  5b). Each band was collected and concentrated, yielding 1.3 mg (1), 2.1 mg (2), and 1.8 mg (3). One of the obtained bands showed a high purity since other bands were not observed under visible and UV light (Fig 5c).

Discussion
Actinobacteria can be used in the bioconversion of agricultural wastes into high-value chemical products. The bioconversion of these wastes is catalyzed by a number of enzymes which are responsible for waste degradation [1]. The Streptomyces genus has been particularly highlighted because its species possess the potential to secrete broad range of enzymes, which could be involved in the production of antibiotics and biopigments [46,47]. Therefore, enzymatic characterization with ApiCoryne stripes allows us to identify the production of different enzymes in an easy and fast way. In our study, Streptomyces sp. strains SO6, PM1, and PM7 presented a high biochemical activity, being positive for at least 12 of the 13 enzymes tested. Moreover, the three preselected strains were capable of fermenting sugars and showed proteolytic and amylolytic activity, with the latter related with the conversion of starch into shorter polymers of glucose units [48]. The biochemical characteristics of Streptomyces spp. SO6 and PM7 granted them the potential to bioconvert starch-rich wastes into interesting bioactive chemicals, including antifungals and biopigments. In our study, we observed different behaviors among the tested Streptomyces strains, where strain SO6 stood out due to its ability to maintain antifungal activity against the three target fungi and produce biopigment in PW medium.
Numerous works reported the production of bioactive compounds by Actinobacteria strains using various commercial media, such as ISP2-7 [43,44]. The replacement of these frequently used commercial media with available and low-cost agro-industrial wastes is an advantage for the sustainable industrial production of antibiotics and biopigments. The Streptomyces genus has a complex development and differentiation, which can adapt to complex and changing environments by ingenious regulation while producing characteristic secondary metabolites [49]. In our study, a noticeable change in pH of the culture media was observed during the fermentation assay using PW broth and ISP2 medium. When Streptomyces SO6 was grown in PW medium, the pH increased to 8 on the second day of incubation, which could favor the degradation of the PW and the release of reducing sugars [50]. The pH increase can be attributable to the assimilation of carbon sources other than starch, with the subsequent release of alkaline byproducts [51]. The release of reducing sugars also coincided with the increase in total proteins on the third day of incubation, reflecting not only the level of extractable proteins originating from the bacterial biomass and PW but also secreted enzymes [52]. Thus, the amylolytic and proteolytic activities of Streptomyces sp. SO6 could also be involved in PW solubilization and, therefore, in the increase in reducing sugars and the decrease in total dry weight. In this way, the solubilization of PW and its colonization by Streptomyces SO6 hindered the determination of the growth rate in the PW medium. An alternative to evaluate bacterial growth rate is the use of agro-industrial waste suspensions as substrate prepared by filtration or boiling [33]. However, a quantity of waste could be generated after filtration, generating another disposal waste problem if it is not used in subsequent nutrient recovery processes.
The differences obtained in the synthesis of antifungals and biopigments shown by Streptomyces spp. in ISP2 and PW media could be associated with differences in microbial growth rates [53] and/or the components of the nutritional support [24]. The PW is composed of damaged potato tubers, which have a high starch content between 60% and 70% on a dry basis [54]. Among the carbon sources, starch is one of the most effective nutritional supplements for increasing antibiotic production [24]. Therefore, its nutritional composition makes PW a rich source of starch for the synthesis of different antibiotic compounds. The pH, temperature, and supplement addition are also relevant parameters that can affect the antibiotic production. Yang and Ling [55] reported optimal conditions to synthetize a high concentration of antibiotics by Streptomyces viridifaciens using potato as basal medium. These optimal conditions consisted of an initial pH between 5.8 and 6.0, supplement addition, temperature (26˚C), and incubation time (5 days). Some of these conditions were similar to those considered in our study, where the synthesis and release of diffusible antifungals against B. cinerea were observed. Antibiotics synthesized by Streptomyces spp. against B. cinerea were also reported by Li et al. [16], using wheat seeds as nutritional support to produce and release volatile antifungal compounds. Streptomyces spp. have also been able to produce antibiotics (oxytetracycline) in agricultural wastes with high protein and fiber contents such as groundnut shells [22] and agro-industrial wastes supplemented with starch [23].
The microbial pigment production is also related to the hydrolysis of starch. Long et al. [25] indicated that carbohydrate metabolism can contribute to the supply of metabolic flux for acetyl-CoA formation and the expression of key genes responsible for microbial biopigment production. In our study, the magenta biopigment formation coincided with PW degradation, evidenced by an increment in reducing sugars and total protein content after the fourth day of PW fermentation. The absence of pigment formation in ISP2 broth during submerged fermentation could be explained by the culture composition since most biopigments are secreted under stress conditions [56]. Similar bacterial magenta pigments have been extracted using different organic solvents [57,58]. A pink/red-like pigment (λ max = 534 nm) produced by Streptomyces coelicoflavus was reported by Assia et al. [57]. According to the authors, the spectral characteristics of these pigments are consistent with nonantibiotic hydrophobic anthracyclines with intracellular localization and photosensitivity. Ramesh et al. [59] also reported an antibacterial red pigment (prodiginine) produced by a Streptomyces sp. in commercial culture media (λ max = 528 nm). These studies highlight the potential of Streptomyces genus to offer a wide range of biopigments to substitute the synthetic pigments. Despite the great versatility of the Streptomyces genus for producing bioactive biopigments in different commercial culture media, there are no recent reports on the use of agro-industrial wastes as basal nutrient support for producing Streptomyces pigments.
In addition to the importance of identifying Streptomyces strains for producing high-value bioproducts using agro-industrial wastes as substrate, the extraction method is determinant to achieve high efficiency in isolation and environmental sustainability. In our study, Streptomyces antifungals and biopigments were extracted using EtOAc from cell-free supernatant and biomass, respectively. EtOAc is commonly reported as an efficient solvent to extracts antibiotics from microbial culture filtrates, exhibiting maximum inhibitory zones when compared with extracts obtained using other organic solvents [43]. This solvent is also considered a green solvent recommended to identify new bioactive compounds, allowing the development of sustainable extraction methods and a reduction in the environmental impact of the chemical extraction process [60,61].

Conclusion
The three Streptomyces sp. strains PM1, PM7, and SO6 exhibited interesting antifungal activity and biopigment production. The Streptomyces sp. strain SO6 stood out for its ability to use potato waste for producing both antifungals against the economically important phytopathogen B. cinerea and intracellular biopigments with reddish-purple coloration. Streptomyces pigments were produced after the third day of submerged fermentation in potato waste, when total protein and reducing sugar contents began to increase. Therefore, the biopigment production could be the result of different extracellular enzymes released during the fermentation process. Our finding led to the conclusion that potato waste is a valuable source of nutrients for the simultaneous production of antifungals and biopigments by Streptomyces spp. Studies on the chemical characterization and optimization of culture parameters during potato waste fermentation are in progress to facilitate scale-up of the antifungal and biopigment production with different biotechnological applications.