Slow Hydrolysis Research Articles

Design and preparation of CaFe layered double hydroxides for efficient treatment of fluorinated water deduced by tailored sustained-release of Ca2+

The pollution from fluorinated wastewater is increasingly severe, and its excessive intake can cause significant harm to human health. CaFe-LDH (Layered Double Hydroxides, LDH) is susceptible to hydrolysis, releasing Ca2+ that can cause secondary pollution to water sources, resulting in limited attention from researchers regarding its application in water treatment. This research explored the application of CaFe-LDH in fluorinated water treatment, harnessing its distinct properties for combined defluoridation through precipitation and adsorption. Various CaFe-LDHs with different Ca/Fe ratios were prepared using inexpensive raw materials and calcined to obtain various CaFe-CLDHs (Calcined Layered Double Hydroxides, CLDH). The calcination temperature and the Ca/Fe ratios influence the composition of CaFe-CLDH, thereby determining its hydrolysis capacity. The key intermediate product of CaFe-LDH/CLDH hydrolysis, CaFe2O4, was discovered for the first time, which slow hydrolysis provides crucial sustained-release capacity for Ca2+, increasing the utilization rate of free Ca2+ and significantly enhancing the defluoridation capacity. CaFe-LDH/CLDH exhibits excellent defluoridation capacity, which increases with the rise in Ca/Fe ratio and calcination temperature. The defluoridation capacity of Ca2Fe-LDH was 234.76 mg g−1, while Ca10Fe-CLDH-800 °C exhibited an astonishing defluoridation capacity of 463.16 mg g−1. The defluoridation of CaFe-LDH/CLDH involves a complex coupling reaction process, incorporating precipitation, coagulation, and adsorption, while the hydrolysis process encounters resistance, as confirmed by DFT simulation results that also verify the adsorption capacity of CaFe2O4 for F. This work provides guidance for the treatment of fluorinated water.

Enzyme-enhanced acidogenic fermentation of waste activated sludge: Insights from sludge structure, interfaces, and functional microflora

Anaerobic fermentation is widely installed to recovery valuable resources and energy as CH4 from waste activated sludge (WAS), and its implementation in developing countries is largely restricted by the slow hydrolysis, poor efficiency, and complicate inert components therein. In this study, enzyme-enhanced fermentation was conducted to improve sludge solubilization from 283 to 7728 mg COD/L and to enhance volatile fatty acids (VFAs) yield by 58.6 % as compared to the conventional fermentation. The rapid release of organic carbon species, especially for tryptophan- and tyrosine-like compounds, to outer layer of extracellular polymeric substance (EPS) occurred to reduce the structural complexity and improve the sludge biodegradability towards VFAs production. Besides, upon enzymatic pretreatment the simultaneous exposure of hydrophilic and hydrophobic groups on sludge surfaces increased the interfacial hydrophilicity. By quantitative analysis via interfacial thermodynamics and XDLVO theory, it was confirmed that the stronger hydrophilic repulsion and energy barriers in particle interface enhanced interfacial mass transfer and reactions involved in acidogenic fermentation. Meanwhile, these effects stimulate the fermentation functional microflora and predominant microorganism, and the enrichment of the hydrolytic and acid-producing bacteria in metaphase and the proliferation of acetogenic bacteria, e.g., Rubrivivax (+9.4 %), in anaphase also benefits VFAs formation. This study is practically valuable to recovery valuable VFAs as carbon sources and platform chemicals from WAS and agriculture wastes.

Effect of lysozyme combined with hydrothermal pretreatment on excess sludge and anaerobic digestion

Anaerobic digestion (AD) is widely employed for sludge stabilization and waste reduction. However, the slow hydrolysis process hinders methane production and leads to prolonged sludge issues. In this study, an efficient and eco-friendly lysozyme pre-treatment method was utilized to address these challenges. By optimizing lysozyme dosage, hydrolysis and cell lysis were maximized. Furthermore, lysozyme combined with hydrothermal pretreatment enhanced overall efficiency. Results indicate that: (1) When lysozyme dosage reached 90 mg/g TS after 240 min of pretreatment, SCOD, soluble polysaccharides, and protein content reached their maxima at 855.00, 44.09, and 204.86 mg/L, respectively. This represented an increase of 85.87%, 365.58%, and 259.21% compared to the untreated sludge. Three-dimensional fluorescence spectroscopy revealed the highest fluorescence intensity in the IV region (soluble microbial product), promoting microbial metabolic activity. (2) Lysozyme combined with hydrothermal pretreatment significantly increased SCOD, soluble proteins, and polysaccharide release from sludge, reducing SCOD release time. Orthogonal experiments identified Group 3 as the most effective for SCOD and soluble polysaccharide release, while Group 9 released the most soluble proteins. The significance order of factors influencing SCOD, soluble proteins, and polysaccharide release is hydrothermal temperature > hydrothermal time > enzymatic digestion time.(3) The lysozyme-assisted hydrothermal pretreatment group exhibited the fastest release and the highest SCOD concentration of 8,135.00 mg/L during anaerobic digestion. Maximum SCOD consumption and cumulative gas production increased by 95.89% and 130.58%, respectively, compared to the control group, allowing gas production to conclude 3 days earlier.

Local high concentration alkali field accelerated silicon hydrolysis for hydrogen production

Silicon is considered as a promising portable hydrolytic hydrogen production material due to its abundant raw materials, high theoretical capacity (1600 mL/g) and facile storage. However, the low hydrolysis activity and slow hydrolysis rate of silicon hinder its practical application. To address this issue, we introduced CaH2 to form Si-based composites via a flexible ball milling method. The above composites showed ideal yield (1216 mL/g in 10 min), reaction conversion (95.5%) and fast hydrolysis kinetics (225 mL/(s·g)) in deionized water, which is one of the best hydrolysis performances of Si-based composites so far. The hydrolytic process can be divided into two steps: the splitting hydrolysis of CaH2 and the continuous hydrolysis of Si. Combining the dynamic in-situ structural analysis with the analogue simulation, it can be confirmed that the formation of local high concentration alkali field is the key to promote the complete hydrolysis and achieve high yield and fast kinetics of the composites. The existence of lattice defects was proved and the adsorption of Si to hydroxide ion was proved by theoretical calculation. Our work provided a novel idea for the theoretical design of hydrolytic hydrogen production compounds and promoted the practical application of low cost and portable hydrolytic hydrogen production materials.

Endogenous biopolymer hydrolysis for enhancing short-chain fatty acids recovery from excess sludge: Combination of lysozyme-catalyzing and cation exchange resin-mediated metal regulation

In decades, anaerobic fermentation with short-chain fatty acids (SCFAs) recovery from excess sludge have attained rising attention. However, rigid particulate organic matter (POMs) structure with slow hydrolysis limited anaerobic fermentation performance of excess sludge. Remarkable sludge hydrolysis performance was supposed to be achievable by the synchronous EPS repture and microbial cell lysis. This study clarified the improvement of overall anaerobic fermentation performance by combination treatment of lysozyme (Lyso) catalysis and metal regulation (MR). The Lyso + MR treatment triggered EPS rupture by protein structure deflocculation while catalyzing microbial cell lysis, which promoted massive extracellular and intracellular POMs hydrolysis. As a result, a significant amount of SCOD (5646.67 mg/L) was produced. Such endogenous organic matters hydrolysis led to considerable SCFAs accumulation (3651.14 mg COD/L) through 48-h anaerobic fermentation at 1.75 g/g SS cation-exchange resin and Lyso dosage of 10% (w/w), which was 5.945 times higher than that in the control. Additionally, it suggested that most of the recovered SCFAs remained in fermentative liquid after chemical conditioning and mechanical dewatering towards solid-liquid separation, which provided considerable economic benefit of 363.6–1059.1 CNY/ton SS.

Effect of Synthetic Methodology on the Physicochemical Attributes and Electrocatalytic Activity of NiAl-LDHs for the Oxygen Evolution Reaction.

Layered double hydroxides (LDHs) are promising materials for oxygen evolution reactions (OERs), a key component of water splitting to produce hydrogen and oxygen via water electrolysis. However, the performance of LDHs can be limited by their low surface area and poor accessibility of active sites. In this work, we synthesized highly exfoliated 2D NiAl-LDHs by aqueous miscible solvent treatment method (AMOST) and compared its electrocatalytic efficiency with its analogue synthesised via slow urea hydrolysis. We demonstrate that the exfoliated 2D LDHs prepared by AMOST method have a higher surface area and more active sites than the crystalline LDHs obtained through urea hydrolysis, resulting in a superior OER activity and efficiency. The exfoliated 2D LDHs required a lower overpotential of 280 mV to reach a current density of 50 mA cm-2 and it also outperformed IrO2, a benchmark OER catalyst, in terms of overpotential and stability. We demonstrate that the physicochemical properties of nanosheets derived from NIAl-LDH-based materials are strongly influenced by the synthetic methodology, which affects the exfoliation degree, surface area and active site density. These factors are crucial for improving the OER catalytic performance of these materials, as shown by our results.

Improved net energy recovery in a sludge anaerobic digestion process by coupling an electrochemical system: electrode material and its impact on suspended microbial community.

Despite its great potential to recover energy from waste sludge, anaerobic digestion (AD) still needs to solve issues such as slow hydrolysis and H2 inhibition. This study investigated the effects of coupling microbial electrolysis cell (MEC) with AD on the CH4 yield. Results and analysis show that the CH4 yield was significantly improved in MEC-AD reactors by two factors, i.e., enhanced and accelerated hydrolysis and acidogenesis, and enrichment of hydrogenotrophic methanogens in suspended culture. Compared with graphite rod and carbon fiber brush, carbon felt (CF) as an electrode showed the best performance in terms of net energy output. The CH4 yield of MEC-AD-CF was 40.2 L CH4/kg VS, 92.3% higher than in the control group, and the VS removal rate was also increased by 47.2%. Acetoclastic methanogens were dominant in the control AD reactor, while the relative abundance of Methanobacterium, which is electroactive and known as hydrogenotrophic methanogen, increased to 24.6% in MEC-AD with CF as electrodes.

Insights into the binding of half-sandwich phosphino Ir(III) and Ru(II) complexes to deoxyribonucleic acid, albumin and apo-transferrin: Experimental and theoretical investigation

A group of cytotoxic half-sandwich iridium(III) (Ir(η5-Cp*)Cl2PPh2CH2OH (IrPOH)), (Ir(η5-Cp*)Cl2P(p-OCH3Ph)2CH2OH (IrMPOH)), and ruthenium(II) (Ru(η6-p-cymene)Cl2PPh2CH2OH (RuPOH), Ru(η6-p-cymene)Cl2P(p-OCH3Ph)2CH2OH (RuMPOH)) complexes with phosphine ligands exhibit the ability to (i) slow hydrolysis which is reversed by adding a high NaCl concentration; (ii) oxidation of NADH to NAD+; (iii) induction of cytotoxicity towards various cancer cell lines. Furthermore, we found that RuPOH and RuMPOH selectively inhibit the proliferation of skin cancer cells (WM266-4) while Ir(III) complexes were found to be moderate against prostate cancer cells (DU-145). Herein, to elucidate the cytotoxic effects, we investigated the interaction of these complexes with DNA and serum proteins by gel electrophoresis, fluorescence spectroscopy, and molecular docking studies. Fluorescence spectroscopic data (calf thymus DNA: CT-DNA titration), together with analysis of DNA fragmentation (gel electrophoresis) and molecular docking provided evidence for the multimodal interaction of Ir(III) and Ru(III) complexes with DNA with predominance of intercalation and minor groove binding. All examined complexes caused single-stranded cleavage of the sugar–phosphate backbone of plasmid DNA. The affinity of the complexes for apo-transferrin (apo-Tf) and human serum albumin (HSA) was evaluated by fluorescence emission spectroscopy to calculate the binding constants which suggested a tight and reversible binding. Moreover, ruthenium complexes can mimic the binding of iron compounds to specific biomolecules such as albumin and transferrin better than iridium complexes. In silico study indicate that complexes mostly bind to (i) apo-Tf with a preference for a single binding site and/or (ii) to dock within all the four predicted binding sites of HSA with the predominance of site I which include tryptophan residues of HSA. This class of ruthenium(II) and iridium(III) complexes has unusual features worthy of further exploration in the design of novel anticancer drugs.

Unleashing synergistic potential of microbially enhanced anaerobic co-digestion of petroleum refinery biosludge and yard waste: Impact of nutrient balance and microbial diversity

Petroleum refinery sludge, an egregious solid residue generated from the wastewater treatment plants poses an environmental hazard owing to its intricate hydrocarbon composition, necessitating competent treatment for secure disposal. The study proposes a green solution through anaerobic co-digestion of nitrogen-rich petroleum refinery sludge (PS) with carbon-rich yard waste (YW), balancing the nutrients and moisture content for efficient microbial proliferation. Using Central Composite Design-Response Surface Methodology, 1 L batch experiments were conducted with varying carbon/nitrogen (C/N) ratios and pH to achieve maximum biogas yield within 50 days of co-digestion. However, the sluggish biogas recovery (40%) indicated a slow rate-limiting hydrolysis, necessitating pretreatment. Feedstock incubation with Bacillus subtilis IH1 strain, isolated from the microbially-enriched PS, at 108 colony forming units (CFU) per mL for 5 days maximized the soluble chemical oxygen demand and volatile fatty acids by 2.2 and 1.4 folds respectively compared to untreated feedstock. Scale-up Bacillus subtilis aided co-digestion studies further augmented biogas by 76% against untreated monodigestion of PS with significant total petroleum hydrocarbons, emulsions, and lignocellulosic degradation. Further identification of major organic pollutants in the batch digestate revealed significant degradation of the toxic organic hydrocarbon pollutants apotheosizing the efficacy of the synergistic sustainable technique for the management of PS. Environmental implicationThe effluent treatment plants (ETPs) of petroleum refining industries generate sludge which is a complex mixture of petroleum hydrocarbons, oil–water (O/W) emulsions and heavy metals. These petroleum hydrocarbon constituents can be linear/cyclic alkanes, polyaromatics, resins and asphaltenes, whose intricate composition is reportedly carcinogenic, cytogenic and mutagenic, classifying it as hazardous waste. Biological treatment of these sludge through anaerobic digestion leads to utilization of petroleum hydrocarbons with subsequent energy recovery. Co-digestion of these sludge with competent co-substrates leads to nutrient balance, diverse microbial proliferation and toxicant dilution. Microbially aided co-digestion further augments methane rendering a digestate with utmost pollutant degradation.

Factors influencing the enzymatic hydrolysis of soy molasses into fermentation feedstock

Soybean processing generates huge amounts of soy molasses that can support biorefinery but require development of waste-to-value conversion technologies. Here, soy molasses processing by Aspergillus niger enzymes was studied to optimize the conversion of oligosaccharides to monomeric sugars as ready fermentation feedstock. The effects of pH and temperature were first investigated using fixed enzyme composition and loading. pH, in the tested 3.0–6.5 range, significantly affected hydrolysis particularly in galactose release. The hydrolysis was fastest at pH 4.8 and 60 °C although the 48-h sugar (glucose, fructose, and galactose) yields were similar at pH 4.8 and 5.7, and 50 and 60 °C. Study was next made at these favorable pH and temperatures using different enzyme compositions and loadings. Glucose and fructose were effectively released, reaching ∼100 % yields in 24–48 h by most of the enzymes and loadings evaluated. Galactose production was less effective and varied significantly with the pH-temperature condition and enzyme loading and composition. Mechanistic evaluation suggested formation and accumulation of galactose disaccharide, whose slow hydrolysis was rate-limiting in the systems with complete glucose and fructose releases but low galactose yields. Model equations were developed to describe the kinetic sugar-release profiles and make technoeconomic analysis, which showed that a process of lower enzyme loading, while requiring longer duration, is more economical within the analyzed range of 5–50 (U α-galactosidase/g molasses). With 5 (U/g) loading, the total cost is about 30 % lower at 60 °C-pH 5.7 than 50 °C-pH 4.8. The α-galactosidase-to-sucrase ratio plays a less significant role in affecting the overall process cost.

Abstract EC.03: Distinct Molecular Signatures Of HCM- And DCM-causing Mutations At The Same Residue In The Transducer Of Cardiac Myosin

Mutations in cardiac myosin cause both hypertrophic (HCM) and dilated cardiomyopathy (DCM), and the clinical phenotype ultimately depends on the precise effect of the mutation on the function of myosin. Using recombinant human cardiac myosin, we studied the molecular effects of a novel Q222H mutation in MYH7 found in a patient with severe, early-onset DCM, and compared the effects to the Q222K mutation that was previously reported to cause HCM. The Q222 residue is located within the transducer of the head domain near the ATP binding pocket. The Q222H (DCM) mutant myosin exhibited significantly reduced steady-state actin-activated ATPase activity and a decreased rate of ATP binding in transient kinetic studies, while Q222K (HCM) mutant protein showed an increase in ATPase activity and ATP binding kinetics. In vitro motility assays showed 43% reduction and 32% increase in actin gliding velocity in Q222H and Q222K mutations, respectively. Finally, single nucleotide turnover assays revealed that the fraction of myosin with a slow ATP hydrolysis rate (super relaxed state, or SRX) thought to represent myosin in an autoinhibited state was significantly reduced in Q222K and increased in Q222H. Taken together, the Q222H/K mutations exerted contrasting effects on the motor properties of the cardiac myosin catalytic domain. Cellular characterization and molecular dynamic simulations of cardiac myosin to assess the structural impact of mutant residues are underway. These results highlight how subtle structural differences between cardiomyopathy-causing mutations can lead to significant differences in cardiac myosin motor activity and thus phenotypic expression of cardiomyopathy.

Insights into the fate and properties of organic halamines during ultraviolet irradiation: Implications for drinking water safety

Organic halamines compounds present a significant threat to the safety of drinking water due to their potential toxicity and stability. While Ultraviolet (UV) disinfection is commonly used for water treatment, its specific effects on organic halamines and the underlying mechanisms remain poorly understood. In this study, we investigated eight amino acid-derived organic chlor- and bromamines as representative compounds. Our findings revealed that organic halamines have a slow hydrolysis rate (<10−3 M−1 s−1) and can persist in water for extended periods (30–2000 min). However, their disinfection efficacy against Staphylococcus aureus and their ability to degrade micropollutants like carbamazepine were found to be limited. Interestingly, under UV irradiation, the N-X bonds in organic halamines were observed to break, leading to accelerated decomposition and the generation of abundant free radicals. These free radicals synergistically facilitated the removal of micropollutants and the inactivation of pathogenic microorganisms. It is worth noting that this transformation of organic halamines during UV disinfection resulted in a slight increase in the concentrations of nitrogenous disinfection byproducts. These findings shed light on the behavior and characteristics of organic halamines during UV disinfection processes, providing crucial insights for effectively managing drinking water quality impacted by these compounds. By understanding the implications of organic halamines, we can refine water treatment strategies and ensure the safety of drinking water supplies.

Slow digestion properties of long-sized isomaltooligosaccharides synthesized by a transglucosidase from Thermoanaerobacter thermocopriae.

Isomaltooligosaccharides (IMOs) are widely used as prebiotic ingredients that promote colon health; however, recent studies revealed that these are slowly hydrolyzed to glucose within the small intestine. Here, novel α-glucans with a higher number of α-1,6 linkages were synthesized from maltodextrins using the Thermoanaerobacter thermocopriae-derived transglucosidase (TtTG) to decrease susceptibility to hydrolysis and improve slow digestion properties. The synthesized long-sized IMOs (l-IMOs; 70.1% of α-1,6 linkages), comprising 10-12 glucosyl units, exhibited slow hydrolysis to glucose when compared to commercial IMOs under treatment with mammalian α-glucosidase level. In male mice, the ingestion of l-IMOs significantly decreased the post-prandial glycemic response compared to other samples (p<0.05). Therefore, enzymatically synthesized l-IMOs can be applied as functional ingredients for the modulation of blood glucose homeostasis in obesity, Type 2 diabetes, and other chronic diseases.

Autohydrolysis of Diglycine‐Activated Succinic Esters Boosts Cellular Uptake

AbstractRapid cellular uptake of synthetic molecules remains a challenge, and the motif frequently employed to generate prodrugs, succinic ester, unfortunately lowers the efficacy of the desired drugs due to their slow ester hydrolysis and low cell entry. Here we show that succinic ester‐containing diglycine drastically boosts the cellular uptake of supramolecular assemblies or prodrugs. Specifically, autohydrolysis of the diglycine‐activated succinic esters turns the nanofibers of the conjugates of succinic ester and self‐assembling motif into nanoparticles for fast cellular uptake. The autohydrolysis of diglycine‐activated succinic esters and drug conjugates also restores the efficacy of the drugs. 2D nuclear magnetic resonance (NMR) suggests that a “U‐turn” of diglycine favors intramolecular hydrolysis of diglycine‐activated succinic esters to promote autohydrolysis. As an example of rapid autohydrolysis of diglycine‐activated succinic esters for instant cellular uptake, this work illustrates a nonenzymatic bond cleavage approach to develop effective therapeutics for intracellular targeting.

Autohydrolysis of Diglycine-Activated Succinic Esters Boosts Cellular Uptake.

Rapid cellular uptake of synthetic molecules remains a challenge, and the motif frequently employed to generate prodrugs, succinic ester, unfortunately lowers the efficacy of the desired drugs due to their slow ester hydrolysis and low cell entry. Here we show that succinic ester-containing diglycine drastically boosts the cellular uptake of supramolecular assemblies or prodrugs. Specifically, autohydrolysis of the diglycine-activated succinic esters turns the nanofibers of the conjugates of succinic ester and self-assembling motif into nanoparticles for fast cellular uptake. The autohydrolysis of diglycine-activated succinic esters and drug conjugates also restores the efficacy of the drugs. 2D nuclear magnetic resonance (NMR) suggests that a "U-turn" of diglycine favors intramolecular hydrolysis of diglycine-activated succinic esters to promote autohydrolysis. As an example of rapid autohydrolysis of diglycine-activated succinic esters for instant cellular uptake, this work illustrates a nonenzymatic bond cleavage approach to develop effective therapeutics for intracellular targeting.

Effect of pH and protein composition on proteolysis of goat milk proteins by pepsin and pancreatin

The roles of protein composition, pH and enzymes in goat milk protein hydrolysis is still unclear and the proteolysis of low abundant goat milk proteins has received limited attention. The aim of this study was to study the impact of protein composition and proteolytic conditions on goat milk protein hydrolysis in a simplified digestion model. Both whole milk and infant formula were hydrolyzed at pH 2 and 4, using pepsin as well as pepsin combined with pancreatin. Intact proteins were separated from digests using spin filters, followed by bottom-up proteomics of the separated proteins. Results show that under all conditions, caseins are hydrolyzed quickly. Goat casein hydrolysis in infant formula was slightly faster than in goat whole milk, possibly due to less casein coagulation during pepsin hydrolysis at both pH 2 and 4. Several low abundant immunoactive goat milk proteins, especially immunoglobulins, GLYCAM-1 and osteopontin, resisted proteolysis more than high abundant proteins, independent of the pH and enzyme used for hydrolysis. Fast hydrolysis of casein and slow hydrolysis of immunoactive proteins may indicate a good balance between protein utilization and protection of the infant by goat milk proteins.

Subtle introduction of membrane polarization-catalyzed H2O dissociation actuates highly efficient electrocoagulation for hardness ion removal

Electrocoagulation represents a promising process for hardness removal from cooling water. Nevertheless, the slow hydrolysis reaction severely restricted the floc formation, inhibiting the hardness co-precipitation and simultaneously causing secondary pollution from dissolved Al3+. Inspired by the detrimental membrane fouling phenomenon in conventional electrodialysis, we reported a rational strategy to substantially enhance the hardness removal efficiency in electrocoagulation by introducing a special membrane polarization-catalyzed H2O dissociation herein. Leveraging the electron transfer between functional groups (–SO3− and –N(CH3)3+) of ion exchange membrane (IEM) and surface-adsorbed H2O under the electric field-induced ion depletion scenario, H2O dissociation could be effectively catalyzed, with this catalytic activity more intensive in –SO3− than in –N(CH3)3+. Such a special H2O dissociation beneficially created a widely distributed and well-simulated alkalinity zone around the anodic region of IEM, which promoted the conversion of dissolved Al3+ to floc Al, thereby enhancing floc formation and circumventing secondary pollution. All these features enabled the resulting membrane-enhanced electrocoagulation (MEEC) to achieve a super-prominent hardness removal rate of 318.9 g h−1 m−2 with an ultra-low specific energy consumption of 3.8 kWh kg−1 CaCO3, considerably outperforming those of other conventional hardness removal processes reported to date. Additionally, in conjunction with a facile air-scoured washing method, MEEC exhibited excellent stability and universal applicability in various reaction conditions.

Quality assessment of japonica brown rice J02 (Oryza sativa L. J02) and its hydrolysis ability for the production of a rice-based drinkcontaining an abundance of dextrin

Plant-based beverages have become very popular in recent emerging markets. Brown rice milk offers several important health benefits because of its various nutritional ingredients such as proteins, carbohydrates, gamma-aminobutyric acid (GABA), and essential vitamins and minerals. Brown rice milk is also low in fats and cholesterol and free of lactose. In this study, japonica brown rice J02 from Thanh Hoa Province presented high nutrition with high protein (8.6% dm) and lipid (2.2% dm) contents as calculated from dry matter and GABA contents of 32 mg/100 g, which is suitable for the plant-based milk processing. J02 rice is also capable of hydrolysis to obtain high molecular sugar in the liquor with slow digestion ability (dextrose equivalent - DE&lt;40) and high hydrolysis efficiency (up to more than 90%). The results obtained from HPLC analysis indicated that the hydrolysis conditions for the rice drink at 75oC and 150 g/l starch produced Spezyme alpha concentrations at 0.024%w/w and low content in low molecular oligosaccharide (DP&lt;10) in the solution. The results indicated that Japonica rice J02 is a good candidate for the production of a rice-based drink.

Slow starch hydrolysis of non-glutinous rice flour and potato starch heated with taxifolin: contribution of proteins to the former and longer amylose to the latter

Taxifolin (dihydroquercetin), which has various pharmacological functions, is contained in edible plants. Some taxifolin-containing foodstuffs such as adzuki bean and sorghum seeds are cooked by themselves and with other starch-containing ingredients. In this study, non-glutinous rice flour (joshin-ko) and potato starch were heated with taxifolin. The heating resulted in the slowdown of pancreatin-induced hydrolysis of suspendable starch in joshin-ko and soluble starch in potato starch. The products of taxifolin formed by the heating such as quercetin were combined with starch during the heating and/or retrogradation, which was converted into the suspendable starch in joshin-ko and the soluble starch in the potato. Taking the difference in protein content and amylose chain length between joshin-ko and potato starch into account, the slowdown is discussed to be due to the binding of the reaction products of taxifolin to proteins in suspendable starch in joshin-ko and to soluble amylose in potato starch.

Effect and mechanism analysis of dual enzyme pretreatment on enhancement of volatile fatty acids production in kitchen waste anaerobic acidification

The high content of cellulose and hemicellulose in kitchen waste (KW) results in a slow hydrolysis rate and subsequently hinders the yields of volatile fatty acids (VFAs) in anaerobic acidification. In this study, cellulase and hemicellulase were used for the pretreatments of KW to tackle the problem of difficult hydrolysis in anaerobic acidification. The results indicated that the joint use of double enzymes significantly improved the hydrolysis of cellulose and hemicellulose during pretreatment, thus enhancing the VFAs production in anaerobic acidification. The highest production of TVFAs was 50.73 ± 2.10 g COD/L and it was improved by 62.77% compared with the unpretreated group. In addition, the 16S rRNA amplicon sequencing analysis showed that the relative abundance of Firmicutes related with the VFAs production increased from 17.77% to 50.55%. The potential metabolism function analysis (PICRUSt2) indicated that the enrichment of glyceraldehyde-3-phosphate dehydrogenase (EC:1.2.1.9) and acetyl-CoA C-acetyltransferase (EC:2.3.1.9) contributed to the production of VFAs in AD. The results suggested that collaborative enzyme pretreatment could be one of the effective methods for the hydrolysis of cellulose and hemicellulose in KW and provided constructive mechanistic insights into recovering valuable products from KW.