Endogenous cAMP elevation in Brassica napus causes changes in phytohormone levels.

In higher plants, the regulatory roles of cAMP (cyclic adenosine 3',5'-monophosphate) signaling remain elusive until now. Cellular cAMP levels are generally much lower in higher plants than in animals and transiently elevated for triggering downstream signaling events. Moreover, plant adenylate cyclase (AC) activities are found in different moonlighting multifunctional proteins, which may pose additional complications in distinguishing a specific signaling role for cAMP. Here, we have developed rapeseed (Brassica napus L.) transgenic plants that overexpress an inducible plant-origin AC activity for generating high AC levels much like that in animal cells, which served the genetic model disturbing native cAMP signaling as a whole in plants. We found that overexpression of the soluble AC activity had significant impacts on the contents of indole-3-acetic acid (IAA) and stress phytohormones, i.e. jasmonic acid (JA), abscisic acid (ABA), and salicylic acid (SA) in the transgenic plants. Acute induction of the AC activity caused IAA overaccumulation, and upregulation of TAA1 and CYP83B1 in the IAA biosynthesis pathways, but also simultaneously the hyper-induction of PR4 and KIN2 expression indicating activation of JA and ABA signaling pathways. We observed typical overgrowth phenotypes related to IAA excess in the transgenic plants, including significant increases in plant height, internode length, width of leaf blade, petiole length, root length, and fresh shoot biomass, as well as the precocious seed development, as compared to wild-type plants. In addition, we identified a set of 1465 cAMP-responsive genes (CRGs), which are most significantly enriched in plant hormone signal transduction pathway, and function mainly in relevance to hormonal, abiotic and biotic stress responses, as well as growth and development. Collectively, our results support that cAMP elevation impacts phytohormone homeostasis and signaling, and modulates plant growth and development. We proposed that cAMP signaling may be critical in configuring the coordinated regulation of growth and development in higher plants.

Antibacterial Conductive Collagen-Based Hydrogels for Accelerated Full-Thickness Wound Healing.

Antibacterial conductive hydrogels have been extensively utilized in tissue repair and regeneration on account of their unique electrochemical performances and advantages of anti-pathogenic bacterial infection. Here, multi-functional collagen-based hydrogels (CHLY) with adhesivity, conductivity, and antibacterial and antioxidant activities were developed by introducing cysteine-modified ε-poly(l-lysine) (ε-PL-SH) and in situ-polymerized polypyrrole (PPy) nanoparticles to induce full-thickness wound healing. CHLY hydrogels have a low swelling ratio, good compressive strength, and viscoelasticity due to chemical crosslinking, chelation, physical interaction, and nano-reinforcements in the matrix network of hydrogels. CHLY hydrogels possess excellent tissue adhesion ability, low cytotoxicity, enhanced cell migration ability, and good blood coagulation performance without causing hemolysis. Interestingly, the chemical conjugation of ε-PL-SH in the hydrogel matrix gives hydrogels an inherently robust and broad-spectrum antibacterial activity, while the introduction of PPy endows hydrogels with superior free radical scavenging capacity and good electroactivity. Significantly, CHLY hydrogels have advantages in alleviating persistent inflammatory response as well as promoting angiogenesis, epidermis regeneration, and orderly collagen deposition at the wound sites through their multi-functional synergies, thus effectively accelerating full-thickness wound healing and improving wound healing quality. Overall, our developed multi-functional collagen-based hydrogel dressing demonstrates promising application prospects in the field of tissue engineering to induce skin regeneration.

Regulation of the autochthonous microbial community in excess sludge for the bioconversion of carbon dioxide to acetate without exogenic hydrogen.

The autochthonous microbial community from excess sludge was regulated for enhanced conversion of CO2 to acetate without exogenic H2. It was interesting that the acetate-fed system exhibited a surprising performance to regulate the microbial community for a high acetate yield and selectivity. As a result, some hydrogen-producing bacteria (e.g., Proteiniborus) and acetogenic bacteria with the ability of CO2 reduction were enriched by acetate feeding, 2-bromoethanesulfonate (BES) addition and CO2 stress. When the selected microbial community was applied to convert CO2, the accumulation of acetate was positively correlated to the concentration of yeast extract. Finally, the acetate yield reached up to 67.24 mM with a high product selectivity of 84 % in the presence of yeast extract (2 g/L) and sufficient CO2 in semi-continuous culture for 10 days. This work should help get new insights into the regulation of microbial community for the efficient acetate production from CO2.

Microstructural tailoring of porous few-layer graphene-like biochar from kitchen waste hydrolysis residue in molten carbonate medium: Structural evolution and conductive additive-free supercapacitor application.

Biomass-derived graphene-like material is a promising candidate for supercapacitor electrodes, while it is critical to controllably convert biomass into structure-tunable graphene. Herein, few-layer graphene-like biochar (FLGBS) was successfully fabricated from waste biomass in molten carbonate medium. Molten carbonate acted as the effective catalyst for graphitizing and the liquid medium for microcrystal relinking to achieve the rearrangement of carbon structure. It was found that the stacking of graphene layer and formation of porous structure were influenced by the volume of reaction medium and biomass pre­carbonation. Namely, increasing the dosage of molten K2CO3 was in favor to form few layer-type graphene structure, but excess dosage could destroy the nanopore structure to expand the aperture. In addition, pre­carbonation at high temperature impeded the exfoliation of graphene layers. When FLGBSs were applied to fabricate conductive additive-free electrode, they displayed a superior supercapacitor performance (up to 237.4 F g-1 at 0.5 Ag-1). This excellent performance should be attributed to the large specific surface area, hierarchical pore structure and graphene-like structure. In short, this work could help to get insights into the structural evolution of biomass carbon to graphene-like biochar in molten carbonate medium and achieve the tailoring of microstructure for further application in energy storage.

GhCNGC13 and 32 Act as Critical Links between Growth and Immunity in Cotton.

Cyclic nucleotide-gated ion channels (CNGCs) remain poorly studied in crop plants, most of which are polyploid. In allotetraploid Upland cotton (Gossypium hirsutum), silencing GhCNGC13 and 32 impaired plant growth and shoot apical meristem (SAM) development, while triggering plant autoimmunity. Both growth hormones (indole-3-acetic acid and gibberellin) and stress hormones (abscisic acid, salicylic acid, and jasmonate) increased, while leaf photosynthesis decreased. The silenced plants exhibited an enhanced resistance to Botrytis cinerea; however, Verticillium wilt resistance was weakened, which was associated with LIPOXYGENASE2 (LOX2) downregulation. Transcriptomic analysis of silenced plants revealed 4835 differentially expressed genes (DEGs) with functional enrichment in immunity and photosynthesis. These DEGs included a set of transcription factors with significant over-representation in the HSF, NAC, and WRKY families. Moreover, numerous members of the GhCNGC family were identified among the DEGs, which may indicate a coordinated action. Collectively, our results suggested that GhCNGC13 and 32 functionally link to photosynthesis, plant growth, and plant immunity. We proposed that GhCNGC13 and 32 play a critical role in the "growth-defense tradeoff" widely observed in crops.

Dynamic Expression, Differential Regulation and Functional Diversity of the CNGC Family Genes in Cotton.

Cyclic nucleotide-gated channels (CNGCs) constitute a family of non-selective cation channels that are primarily permeable to Ca2+ and activated by the direct binding of cyclic nucleotides (i.e., cAMP and cGMP) to mediate cellular signaling, both in animals and plants. Until now, our understanding of CNGCs in cotton (Gossypium spp.) remains poorly addressed. In the present study, we have identified 40, 41, 20, 20, and 20 CNGC genes in G. hirsutum, G. barbadense, G. herbaceum, G. arboreum, and G. raimondii, respectively, and demonstrated characteristics of the phylogenetic relationships, gene structures, chromosomal localization, gene duplication, and synteny. Further investigation of CNGC genes in G. hirsutum, named GhCNGC1-40, indicated that they are not only extensively expressed in various tissues and at different developmental stages, but also display diverse expression patterns in response to hormones (abscisic acid, salicylic acid, methyl jasmonate, ethylene), abiotic (salt stress) and biotic (Verticillium dahlia infection) stimuli, which conform with a variety of cis-acting regulatory elements residing in the promoter regions; moreover, a set of GhCNGCs are responsive to cAMP signaling during cotton fiber development. Protein-protein interactions supported the functional aspects of GhCNGCs in plant growth, development, and stress responses. Accordingly, the silencing of the homoeologous gene pair GhCNGC1&18 and GhCNGC12&31 impaired plant growth and development; however, GhCNGC1&18-silenced plants enhanced Verticillium wilt resistance and salt tolerance, whereas GhCNGC12&31-silenced plants had opposite effects. Together, these results unveiled the dynamic expression, differential regulation, and functional diversity of the CNGC family genes in cotton. The present work has laid the foundation for further studies and the utilization of CNGCs in cotton genetic improvement.

Molecular Targets and Biological Functions of cAMP Signaling in Arabidopsis.

Cyclic AMP (cAMP) is a pivotal signaling molecule existing in almost all living organisms. However, the mechanism of cAMP signaling in plants remains very poorly understood. Here, we employ the engineered activity of soluble adenylate cyclase to induce cellular cAMP elevation in Arabidopsis thaliana plants and identify 427 cAMP-responsive genes (CRGs) through RNA-seq analysis. Induction of cellular cAMP elevation inhibits seed germination, disturbs phytohormone contents, promotes leaf senescence, impairs ethylene response, and compromises salt stress tolerance and pathogen resistance. A set of 62 transcription factors are among the CRGs, supporting a prominent role of cAMP in transcriptional regulation. The CRGs are significantly overrepresented in the pathways of plant hormone signal transduction, MAPK signaling, and diterpenoid biosynthesis, but they are also implicated in lipid, sugar, K+, nitrate signaling, and beyond. Our results provide a basic framework of cAMP signaling for the community to explore. The regulatory roles of cAMP signaling in plant plasticity are discussed.

Technical framework for wastewater-based epidemiology of SARS-CoV-2.

Wastewater-based epidemiology (WBE) is expected to become a powerful tool to monitor the dissemination of SARS-CoV-2 at the community level, which has attracted the attention of scholars all over the world. However, there is not yet a standard protocol to guide its implementation. In this paper, we proposed a comprehensive technical and theoretical framework of relative quantification via qPCR for determining the virus abundance in wastewater and estimating the infection ratio in corresponding communities, which is expected to achieve horizontal and vertical comparability of the data using a human-specific biomarker as the internal reference. Critical factors affecting the virus detectability and the estimation of infection ratio include virus concentration methods, lag-period, per capita virus shedding amount, sewage generation rate, temperature-related decay kinetics of virus/biomarker in wastewater, and hydraulic retention time (HRT), etc. Theoretical simulation shows that the main factors affecting the detectability of virus in sewage are per capita virus shedding amount and sewage generation rate. While the decay of SARS-CoV-2 RNA in sewage is a relatively slow process, which may have limited impact on its detection. Under the ideal condition of high per capita virus shedding amount and low sewage generation rate, it is expected to detect a single infected person within 400,000 people.

Isolation, production and optimization of endogenous alkaline protease from in-situ sludge and its evaluation as sludge hydrolysis enhancer.

Bioconversion (e.g. anaerobic fermentation and compost) is the common recycling method of waste activated sludge (WAS) and its hydrolysis, as the rate-limiting step of fermentation, could be accelerated by protease. However, the commercial protease was unstable in a sludge environment, which increased the cost. An endogenous alkaline protease stable in sludge environment was screened in this study and its suitability for treating the sludge was analyzed. The optimal production medium was determined by Response Surface Methodology as starch 20 g/L, KH2PO4 4 g/L, MgSO4·7H2O 1 g/L, sodium carboxy-methyl-cellulose 4 g/L, casein 4 g/L and initial pH 11.3, which elevated the yield of protease by up to 15 times (713.46 U/mL) compared with the basal medium. The obtained protease was active and stable at 35 °C-50 °C and pH 7.0-11.0. Furthermore, it was highly tolerant to sludge environment and maintained high efficiency of sludge hydrolysis for a long time. Thus, the obtained protease significantly hydrolyzed WAS and improved its bioavailability. Overall, this work provided a new insight for enzymatic treatment of WAS by isolating the endogenous and stable protease in a sludge environment, which would promote the resource utilization of WAS by further bioconversion.

Molten salt induced nitrogen-doped biochar nanosheets as highly efficient peroxymonosulfate catalyst for organic pollutant degradation.

Advanced oxidation processes based on carbon catalysis is a promising strategy possessing great potential for environmental pollution degradation. Herein, nitrogen-doped biochar nanosheets (NCS-x) were synthesized using a nitrogen-rich biomass (Candida utilis) as sole precursor. The involvement of environmental-friendly molten salt (NaCl and KCl) in pyrolysis process not only facilitated the exfoliation of biochar, but also favored the retention of N element in biochar. When applying as catalyst for peroxymonosulfate activation, the as-obtained NCS-6 exhibited outstanding performance in catalytic degradation of bisphenol A (BPA). A 100% removal efficiency was observed in 6 min with fast reaction kinetic (k = 1.36 min-1). Based on quenching test and in-situ electron paramagnetic resonance analysis, both radical pathway and non-radical pathway were suggested to be involved in BPA degradation, while singlet oxygen was identified as the dominant reactive oxygen species. Furthermore, the ecotoxicity evaluation using Chlorella vulgaris as ecological indicator indicated that BPA solution after degradation was less toxic than the original solution. It is expected that this green and facile strategy holds great promise for value-added conversion of nitrogen-rich biomass to highly efficient biochar nanosheets for environment remediation.

Enhanced Cr(VI) removal by waste biomass derived nitrogen/oxygen co-doped microporous biocarbon.

Herein, kitchen waste hydrolysis residue (KWHR) was utilized as the precursor to fabricate nitrogen/oxygen co-doped microporous biocarbons (NOMBs) with ultrahigh specific surface area via KOH activation. Activation temperature was found to be crucial for heteroatom doping and pore structure construction. Attractively, the obtained NOMB with high surface area (2417 m2/g) and microporosity (~ 90%) displayed an outstanding capacity of Cr(VI) removal (526.1 mg/g at pH 2). The kinetics and isotherm studies showed that the adsorption of Cr(VI) onto NOMB was well described by the pseudo-second-order kinetics and Langmuir isotherm. Moreover, it was found that Cr(VI) was partly reduced to Cr(III) during the removal process as the nitrogen/oxygen functionalities and unsaturated carbon bond played crucial roles of electron-donors, which revealed the fact that the removal of Cr(VI) by NOMB was attributed to the coupling of adsorption and reduction reaction. Overall, this study has demonstrated the possibility of preparing microporous biocarbons using KWHR as a renewable material and the resultant NOMB is of great potential to detoxify Cr(VI).

Efficient adsorption of methylene blue by xanthan gum derivative modified hydroxyapatite.

In this work, hydroxyapatite modified by xanthan gum (XG) derivative material (XMH) was prepared and applied to remove methylene blue (MB) from water. The physicochemical properties of XMH were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, X-Ray spectroscopy and thermogravimetric analysis. Results showed the operating variables (pH, ionic strength and adsorbent dosage) were related to the MB removal efficiency. Adsorption kinetic and adsorption isotherm were well fitted by the pseudo-second-order model and the Langmuir isotherm model, respectively. It indicated that the adsorption process was a monolayer layer adsorption and chemisorption process. Besides, the result of intra-particle diffusion model demonstrated that the intra-particle diffusion was not the only rate determining step. The maximum adsorption capability on MB was 769 mg/g. Thermodynamic parameters (ΔG0, ΔH0, and ΔS0) showed that the adsorption was a spontaneous and endothermic process. Adsorption mechanisms of MB on XMH might be governed by electrostatic attraction and hydrogen-bonding. Furthermore, XMH could be regenerated well and retained MB removal efficiency of 81% after five cycles of adsorption and desorption. Therefore, XMH is a promising adsorbent for the efficient removal of MB from aqueous solution due to its low cost, good thermal stability and excellent adsorption performance.

Hydrothermal route-enabled synthesis of sludge-derived carbon with oxygen functional groups for bisphenol A degradation through activation of peroxymonosulfate.

A considerable amount of sewage sludge (SS) is generated from wastewater treatment process, which is hazardous to the environment and in urge to be disposed. In this study, for the first time, we prepared carbocatalyst with abundant surface oxygen functional groups using the hazardous waste of SS as precursor via a facile hydrothermal coupled pyrolysis process. The hydrothermal treatment was found to be crucial for enhancing the oxygen content of sludge carbon (SC), most of which existed as ketonic groups. Catalytic performances of the developed SCs were examined by activating peroxymonosulfate (PMS) to degrade bisphenol A (BPA). Sample with more ketonic group performed better for BPA degradation. Under optimal reaction conditions, 100 % of BPA and 69.53 % of TOC could be removed in 20 min. Singlet oxygen (1O2) was suggested to be the main reactive oxygen species for degrading BPA and a BPA degradation pathway was proposed. The BPA solution showed decreased bio-toxicity after the oxidation process according to the acute ecotoxicity test. This study demonstrated the importance of surface functional groups on carbocatalyst for advanced oxidation process, which could be induced by a facile hydrothermal treatment. The feasibility of utilizing hazardous SS for advanced carbocatalyst fabrication was also revealed.

One-step synthesis of nitrogen-doped sludge carbon as a bifunctional material for the adsorption and catalytic oxidation of organic pollutants.

Nitrogen-doped carbon (NC) materials have been extensively investigated for their great potential applications in adsorption, catalysis, etc. Herein, we report a facile one-step pyrolysis process for NC synthesis using abundant bio-waste of excess sludge as carbon source and cheap precursor of urea as nitrogen source. The developed materials were evaluated for organic pollutants removal through adsorption and catalytic oxidation by peroxymonosulfate (PMS) activation. Experimental results demonstrated that nitrogen doping significantly affected the elemental composition and microstructure of NC, leading to improved adsorption capability as well as PMS activation activity for methylene blue (MB) removal. The adsorption capacity for MB reached 35.831 mg g-1 over NC-700 sample (NC prepared at 700 °C). In MB catalytic oxidation experiments, effects of sample calcination temperature, catalyst dosage, PMS loading, and co-existing ions were investigated. Under optimal reaction conditions, 98.70% of MB could be removed in 20 min. Through radical quenching and electron spin resonance (ESR) tests, it was confirmed that singlet oxygen (1O2) was the main reactive species for MB degradation. Additionally, NC-700 performed well in recycle studies without significant efficiency loss. Other typical organic pollutants including malachite green (MG), methyl orange (MO), bisphenol A (BPA), phenol (PE), and sulfamethoxazole (SMX) could also be removed using NC-700 as adsorbent and catalyst. These features manifest that excess sludge-derived NC could be a promising material for organic pollutants remediation.

An adsorbent based on humic acid and carboxymethyl cellulose for efficient dye removal from aqueous solution.

Adsorbents from sustainable precursors are highly desirable for practical applications. In this study, carboxymethyl cellulose (CMC) and humic acid (HA) were adopted to fabricate a composite immobilized on precipitates of calcium hydroxide (PCH) and ferric hydroxide (PFH). The as-obtained adsorbent, denoted as HA-CMC/PMH (PCH and PFH were referred to as PMH), was analyzed by infrared spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy and thermo gravimetric analysis. When applying for a typical organic pollutant of methylene blue (MB) removal from aqueous solution, a high adsorption capacity of 666.67 mg/g was achieved over HA-CMC/PMH. The adsorption mechanisms of MB involved ion exchanging and π-π interactions, this adsorption process mainly occurred on both anionic and aromatic groups. Adsorption behavior analysis indicated that Langmuir isotherm model and pseudo-second order kinetic model fitted experimental data well, suggesting a mono-layer adsorption of MB onto the adsorbent. Further thermodynamic analysis proved that the adsorption of MB onto HA-CMC/PMH was an exothermal spontaneous process. The developed adsorbent is also reusable with 79.93% of adsorption capacity remaining in the fifth recycle runs. Therefore, the adsorbent of HA-CMC/PMH is suggested to be a promising candidate for adsorption applications.

Biosynthesis, structure and antioxidant activities of xanthan gum from Xanthomonas campestris with additional furfural.

Lignocellulosic-like materials are potentially low-cost fermentation substrates, but their pretreatment brings about by-products. This work investigated the effects of furfural on xanthan gum (XG) production, and product quality was evaluated by structure, viscosity and antioxidant capacities. Xanthomonas campestris maintained steady polysaccharide yield (above 13 g·L-1) with enhanced cell growth at low furfural concentrations (below 3.2 g·L-1). The products were verified as XG by FT-IR, XRD, NMR and monosaccharide analysis. Moreover, they were found to have reduced acetyl, rising pyruvate and up-to-down glucuronic acid groups as increasing furfural concentration. Furthermore, XG product with 1 g·L-1 furfural addition showed the best hydroxyl scavenging effects, though reducing powers presented no variation. It was demonstrated that furfural, the common hydrolysis by-product, was not necessarily an inhibitor for fermentation, and an appropriate amount of furfural was beneficial to XG production with steady yield and good quality.

Preparation of temperature-sensitive Xanthan/NIPA hydrogel using citric acid as crosslinking agent for bisphenol A adsorption.

Hydrogels are emerging materials in pollutant treatment due to their high absorbability and environmental friendliness. Herein, a novel temperature-sensitive hydrogel based on xanthan gum (XG) and N-isopropylacrylamide (NIPA) was successfully synthesized in a water system using low-cost citric acid as crosslinking agent. The lower critical solution temperature of the honeycomb macroporous XG/NIPA hydrogels was 40 °C. Meanwhile, the hydrogels had good water-absorption capacity and the swelling degree reached up to 70.1. Using XG/NIPA hydrogels to absorb bisphenol A (BPA), the maximum adsorption capacity was as high as 458 mg/g. The process was a multilayer adsorption and the rate-controlling step is chemisorption. Thus, the temperature-sensitive XG/NIPA hydrogel had great potential in absorbing BPA from aqueous solutions.

Effects of deproteinization methods on primary structure and antioxidant activity of Ganoderma lucidum polysaccharides.

Ganoderma lucidum polysaccharides (GLP) as one of water-soluble polysaccharides has attracted much attention because of its bioactivities, especially antioxidant activity. Deproteinization is an essential step in the purification process of polysaccharides. In this study, three classic deproteinization methods, including neutral protease method, TCA precipitation and CaCl2 salting out, were evaluated for crude GLP processing. The methods had ability to remove proteins (71.50-87.36%), and meanwhile polysaccharide loss (8.35-11.39%) was observed. Structure analysis indicated that these deproteinization methods had no significant effect (p > 0.05) on molecular weight of polysaccharides, but led to varying degrees of glycoside bond losses (1.14-64.05%). Moreover, the antioxidant activities of deproteinized polysaccharides were measured in vitro by hydroxyl radical, reducing power, 2, 2-diphenyl-1-picryl-hydrazyl (DPPH) free radical and ferric-reducing antioxidant power tests. Purified GLP by enzymolysis maintained the strongest antioxidants activities with the retention rate of over 47.40%, and its deproteinization efficiency and polysaccharide loss ratio were 74.03% and 11.39% respectively. In view of relatively high purity and antioxidant activity, enzymolysis was a suitable deproteinization method for GLP production.

A new approach for excess sludge reduction by manganese dioxide oxidation: performance, kinetics, and mechanism studies.

A considerable amount of excess sludge, a kind of hazardous waste, is produced from the conventional wastewater treatment systems such as activated sludge process, and efficient sludge reduction processes are needed. A new chemical method for sludge reduction was proposed by using manganese dioxide as oxidant in this study. A favorable condition for sludge reduction is determined as manganese dioxide dosage of 0.165 g g-1 wet sludge, sulfuric acid concentration of 3 mol L-1, and reduction temperature of 90 °C for 90 min, where the sludge reduction efficiency can reach 73.30%. Reaction kinetic study revealed that the sludge reduction rate was controlled by the surface chemical reaction and the reaction followed a shrinking core kinetic model with apparent activation energy of 37.76 kJ mol-1. Furthermore, reaction process analysis indicated that the sludge hydrolysis included two steps, i.e., floc destruction and microbial cell disruption. Considering the high efficiency and short treatment time, manganese dioxide oxidation is suggested to be a feasible method for disintegration of excess activated sludge.

Utilization of Waste Biomass (Kitchen Waste) Hydrolysis Residue as Adsorbent for Dye Removal: Kinetic, Equilibrium, and Thermodynamic Studies.

Kitchen waste hydrolysis residue (KWHR), which is produced in the bioproduction process from kitchen waste (KW), is usually wasted with potential threats to the environment. Herein, experiments were carried out to evaluate the potential of KWHR as adsorbent for dye (methylene blue, MB) removal from aqueous solution. The adsorbent was characterized using FT-IR and SEM. Adsorption results showed that the operating variables had great effects on the removal efficiency of MB. Kinetic study indicated pseudo-second-order model was suitable to describe the adsorption process. Afterwards, the equilibrium data were well fitted by using Langmuir isotherm model, suggesting a monolayer adsorption. The Langmuir monolayer adsorption capacity was calculated to be 110.13 mg/g, a level comparable to some other low-cost adsorbents. It was found that the adsorption process of MB onto KWHR was spontaneous and exothermic through the estimation of thermodynamic parameters. Thus, KWHR was of great potential to be an alternative adsorbent material to improve the utilization efficiency of bioresource (KW) and lower the cost of adsorbent for color treatment.