Physicochemical and functional properties of chitosans affected by storage periods of crab leg shell

Effects of storage period (0, 1, 2, 3 and 4 months) of crab leg shell at room temperature on selected physicochemical and functional properties of E‐ and G‐chitosans, respectively, prepared from entire (E) and ground (G) shells were evaluated. Increased storage period of crab shell generally increased degree of deacetylation (DD) and viscosity, but decreased DPPH radical scavenging activity of both chitosans. Water‐binding (WBC) and fat‐binding (FBC) capacities of E‐chitosan were not affected by storage period of crab shell; however, those of G‐chitosan significantly increased when crab shell was stored for more than 1 month. Dye‐binding capacity (DBC) of both chitosans decreased when crab shell was stored for 1 month, but further decrease was not observed with increased storage period to 4 months. Prepared with 4‐month stored crab shell, E‐chitosan exhibited comparable viscosity, colour whiteness index, DPPH radical scavenging activity and DBC, but lower DD, WBC and FBC than G‐chitosan.     

Preparation and characterisation of selected physicochemical and functional properties of β‐chitosans from squid pen

Squid pen β‐chitosans prepared under various deacetylation conditions (30%, 35%, 40% and/or 45% NaOH for 15, 30 and/or 60 min) were characterised. β‐Chitosans (deacetylated with 35–45% NaOH for 15–60 min) had 87.1–96.2% degree of deacetylation (DD), 93.5–96.7% solubility and 120.5–654.9 mPa s viscosity. Treatment with 30% NaOH for 15–60 min yielded inadequately deacetylated β‐chitosans (DD = 51.9–80.2%). Two chitosans prepared under 35% NaOH for 15 min and 45% NaOH for 30 min (designated as 35%–15 and 45%–30, respectively) were further compared. Drying (sun‐drying vs. oven‐drying) methods did not affect DD. 35%–15 chitosan exhibited lower nitrogen, DD and bulk density, but higher viscosity compared with 45%–30 chitosan. Higher water‐ and fat‐binding capacity but lower DPPH radical scavenging activity were observed for 35%–15 chitosan compared with 45%–30 chitosan. Compared with 45%–30 chitosan, 35%–15 chitosan exhibited higher antibacterial activity against Salmonella Enteritidis and Listeria monocytogenes, but lower antibacterial activity against Escherichia coli.     

Effect of chitosan on Bacillus cereus inhibition and quality of cooked rice during storage

Improper cooling of cooked rice at an inappropriate temperature or leaving cooked rice at room temperature can cause food poisoning attributed to Bacillus cereus. Natural food preservative of either squid or crab polymer chitosan solution was added to examine their antibacterial properties against Bacillus cereus in cooked rice during storage at 37 and 4 °C. Both types of chitosan could retard the growth of B. cereus and total aerobic counts in cooked rice stored at 37 °C up to 1 day. In addition, the effect of chitosans on the physical and textural properties of cooked rice during storage was studied. Both chitosans slightly increased the moisture content of cooked rice. However, chitosans had no effect on the whiteness and hardness of cooked rice during storage (P > 0.05). Therefore, both chitosans have a potential to be used as food preservative for cooked rice with no negative effects on rice quality.     

Antibacterial Activity of Ozone‐Depolymerized Crawfish Chitosan

ABSTRACT: Antimicrobial activities of chitosan samples with different molecular weights (1333, 432, 201, 131, and 104 kDa) prepared by ozone treatment were examined against 2 Gram‐positive bacteria (Listeria monocytogenes and Staphylococcus aureus) and 2 Gram‐negative bacteria (Escherichia coli and Pseudomonas fluorescen) to investigate the effect of chitosan's molecular weight and concentration on the inhibition of bacterial growth. Antimicrobial activity of chitosan varied depending on the molecular weight, concentration of chitosan, and type of microorganism. Generally, the effectiveness of the chitosans significantly increased with increasing chitosan concentration, regardless of molecular size and types of bacteria. Chitosan with molecular weights ranging from 104 to 201 kDa showed relatively greater antimicrobial activity against L. monocytogenes, S. aureus, and P. fluorescen; whereas for E. coli, intermediate molecular weight chitosan was more effective in growth inhibition than lower or higher molecular weight chitosan particularly at 0.1% concentration.     

Antibacterial activity of chitosans with different degrees of deacetylation and viscosities

Antibacterial activities of six acid‐soluble [two degrees of deacetylation (DD) × three viscosities] and two water‐soluble chitosans (two DD with similar viscosities) were examined against eight gram‐negative (Pseudomonas fluorescens, Proteus vulgaris, Erwinia carotovora, Serratia marcescens, Escherichia coli, Vibrio parahaemolyticus, V. vulnificus, and Salmonella Typhimurium) and six gram‐positive bacteria (Listeria monocytogenes, Staphylococcus aureus, Bacillus subtilis, B. cereus, Lactobacillus curvatus, and L. plantarum). Antibacterial activities of chitosans differed depending on the chitosan types and bacteria tested. Water‐soluble chitosans inhibited bacterial growth by one to eight log cycles at 0.1% concentration; however, the effects were much lesser than those observed with 0.05% acid‐soluble chitosans. Minimum inhibitory concentration (MIC) values (0.03% to above 0.1%) of acid‐soluble chitosans were much lower than those (0.05% to above 0.8%) of water‐soluble chitosans. Based on MIC values, the acid‐soluble chitosan with 99% DD and lower viscosity (17.9 mPa s) was most effective in inhibiting bacteria growth among eight chitosans tested.     

Antibacterial activity of chemically defined chitosans: influence of molecular weight, degree of acetylation and test organism

Chitosans, polysaccharides obtained from the exoskeleton of crustaceans, have been shown to exert antibacterial activity in vitro and their use as a food preservative is of growing interest. However, beyond a consensus that chitosan appears to disrupt the bacterial cell membrane, published data are inconsistent on the chemical characteristics that confer the antibacterial activity of chitosan. While most authors agree that the net charge density of the polymer (reflected in the fraction of positively charged amino groups at the C-2 position of the glucosamine unit) is an important factor in antibacterial activity, conflicting data have been reported on the effect of molecular weight and on the susceptibility among different bacterial species to chitosan. Therefore, we prepared batches of water-soluble hydrochloride salts of chitosans with weight average molecular weights (M_w) of 2-224 kDa and degree of acetylation of 0.16 and 0.48. Their antibacterial activity was evaluated using tube inhibition assays and membrane integrity assays (N-Phenyl-1-naphthylamine fluorescence and potassium release) against Bacillus cereus, Escherichia coli, Salmonella Typhimurium and three lipopolysaccharide mutants of E. coli and S. Typhimurium. Chitosans with lower degree of acetylation (F_A = 0.16) were more active than the more acetylated chitosans (F_A = 0.48). No trends in antibacterial action related to increasing or decreasing M_w were observed although one of the chitosans (M_w 28.4 kDa, F_A = 0.16) was more active than the other chitosans, inhibiting growth and permeabilizing the membrane of all the test strains included. The test strains varied in their susceptibility to the different chitosans with wild type S. Typhimurium more resistant than the wild type E. coli. Salmonellae lipopolysaccharide mutants were more susceptible than the matched wild type strain. Our results show that the chitosan preparation details are critically important in identifying the antibacterial features that target different test organisms.     

Enhanced thermal and antibacterial properties of cross‐linked waxy maize starch granules by chitosan via dry heat treatment

Cross‐linked starch was synthesised using chitosan as cross‐linking agent via a dry heating method. Thermal properties measured by DSC showed transition temperatures increased as compared with that of native starch (P < 0.001), which might indicate the starch and chitosan molecules interacted with each other. XRD demonstrated that the crystalline pattern of the starch remained the same, but there was slight change in the crystallinity degree after the cross‐links. The significant reduction of solubility, swelling power and transparency (P < 0.001) indicated that the cross‐links restricted the starch granules swelling and molecules leaching. Agar diffusion test showed that chitosan‐cross‐linked starch had excellent bacterial growth inhibition, and its antibacterial activity was stronger against Gram‐negative bacteria than against Gram‐positive bacteria. Its antibacterial activity was further confirmed using liquid broth method. Thus, the cross‐linked starch may be directly used in the food formula for protecting food as a natural antimicrobial ingredient.     

Effect of Molecular Weight,Acid, and Plasticizer on the Physicochemical and Antibacterial Properties of β‐Chitosan Based Films

Abstract: Effects of chitosan molecular weight (1815 and 366 kDa), type of acid (1% acetic, formic, and propionic acid, or 0.5% lactic acid) and plasticizer (0, 25% glycerol or sorbital w/w chitosan) on the mechanical, water barrier, and antibacterial properties of β‐chitosan films were investigated. Tensile strength (TS) of high molecular weight (Hw) films was 53% higher than that of low molecular weight (Lw) ones, acetate, and propionate films had the highest TS (43 and 40 MPa) among tested acids, and plasticizer‐reduced film TS 34%. Film elongation at break (EL) was higher in Hw films than in Lw ones, in which formate and acetate films were the highest (9% and 8%, respectively), and plasticizer increased the film EL 128%. Molecular weight of chitosan did not influence water vapor permeability (WVP) of the films. Acetate and propionate films had lower WVP than other acid types of films, and plasticizer increased film WVP about 35%. No difference was found between glycerol and sorbitol films in terms of film mechanical and water barrier properties. Lw β‐chitosan films showed significant antibacterial activity against E. coli and L. innocua. This study demonstrated that β‐chitosan films are compatible to α‐chitosan films in physicochemical properties and antibacterial activity, yet with simple sample preparation. Practical Application: β‐chitosan based edible films at molecular weight of about 300 kDa showed great antibacterial activity against Gram‐positive and Gram‐negative bacteria. The films have similar mechanical and water barrier properties to α‐chitosan based films at the similar molecular weight, but simple sample preparation procedures and more attractive color. The release of active chitosan fragment from the film matrix acts as an antibacterial agent, making β‐chitosan films suitable as intelligent food wraps or coatings for a wide range of food products to control moisture loss and prevent surface bacterial growth.     

Preparation of antibacterial chito‐oligosaccharide by altering the degree of deacetylation of β‐chitosan in a Trichoderma harzianum chitinase‐hydrolysing process

BACKGROUND: Chito‐oligosaccharide (COS) is generally known to possess many specific biological functions, especially antibacterial activity, depending on its size. To prepare a specific size range of COS, however, has proved difficult. The aim of this study was to establish a method for preparing a specific size range of antibacterially active COS by adjusting the degree of deacetylation (DD) of β‐chitosan in a Trichoderma harzianum chitinase‐hydrolysing process. RESULTS: The molecular weight spectrum, elucidated by viscosity‐average molecular weight, high‐performance liquid chromatography and thin layer chromatography, of COS in chitosan hydrolysate was significantly related to the DD of its original chitosan. Compared with the original form, COS produced at 90% DD showed superior activity against most Gram‐negative bacteria tested, with a minimum inhibition concentration (MIC) ranging from 55 ± 27 to 200 ± 122 µ g mL^?1. Conversely, most Gram‐positive strains tested were less sensitive to COS (MIC > 880 ± 438 µ g mL^?1) than to its original form. Among the Gram‐positive strains, Staphylococcus xylosus was the only exception in that it showed a high susceptibility to COS and had an MIC as low as 45 ± 11 µ g mL^?1. CONCLUSION: The results indicate that the production of a specific size range of COS product is possible by altering the DD of chitosan in the chitinase‐catalysed process. To produce various sizes of COS for versatile biological functions, as seen in this study to inhibit various types of bacteria, is made possible in this established process. Copyright © 2008 Society of Chemical Industry     

Sorption Behavior of Crawfish Chitosan Films as Affected by Chitosan Extraction Processes and Solvent Types

Effects of chitosan extraction processes and solvent types on sorption behavior of unplasticized crawfish chitosan films were investigated. Four different chitosans prepared from crawfish shell were dissolved in 1% v/v acetic, formic, lactic, or malic acids at 1% w/v concentration. Chitosans dissolved in acetic or formic acid formed flexible and transparent films that are desirable for packaging applications. Chitosan acetate films maintained lower moisture contents at any relative humidity level compared with chitosan formate films. The type of chitosan significantly influenced the sorption isotherms of chitosan formate films but not chitosan acetate films. The Guggenheim‐Anderson‐de Boer, Oswin, and Caurie models (R²= 0.98, 0.95, and 0.95, respectively) could be used to predict sorption behavior of crawfish chitosan acetate and formate films.     

Correlation between Antimicrobial,Antioxidant Activity,and Polyphenols of Alkalized/Nonalkalized Cocoa Powders

Many factors can influence antioxidative and antimicrobial characteristics of plant materials. The quality of cocoa as functional food ingredient is influenced through its processing. The main aim of this study was to test if there is difference in polyphenol content, antioxidant capacity, and antimicrobial activity between nonalkalized and alkalized cocoa powders. To estimate polyphenol and flavonoid content in cocoa samples the spectrophotometric microassays were used. Flavan‐3ols were determined with reversed‐phase high‐performance liquid chromatography (RP‐HPLC). Antimicrobial activity against 3 Gram positive bacteria, 4 Gram negative bacteria and 1 strain of yeast was determined using broth microdilution method. Total polyphenol content was 1.8 times lower in alkalized cocoa samples than in natural ones. Epicatechin/catechin ratio was changed due to the process of alkalization in favor of catechin (2.21 in natural and 1.45 in alkalized cocoa powders). Combined results of 3 antioxidative tests (DPPH, FRAP, ABTS) were used for calculation of RACI (Relative Antioxidant Capacity Index) and GAS (Global Antioxidant Score) values that were consistently higher in natural than in alkalized cocoa extracts. Obtained results have shown significant correlations between these values and phenolic content (0.929 ≤ r ≤ 0.957, P < 0.01). Antimicrobial activity varied from 5.0 to 25.0 mg/ml (MICs), while Candida albicans was the most sensitive tested microorganism. Cocoa powders subjected to alkalization had significantly reduced content of total and specific phenolic compounds and reduced antioxidant capacity (P < 0.05), but their antimicrobial activity was equal for Gram‐positive bacteria or even significantly enhanced for Gram‐negative bacteria.     

Antibacterial Activities of Chitosans and Chitosan Oligomers with Different Molecular Weights on Spoilage Bacteria Isolated from Tofu

Seven bacteria were isolated from spoiled tofu and identified as Bacillus sp. (S08), B. megaterium (S10), B. cereus (S17, S27, S28, S32), and Enterobacter sakazakii (S35). In a paper disc test with 6 chitosans and 6 chitosan oligomers of different molecular weights, chitosans showed higher antimicrobial activity than did chitosan oligomers at a 0.1% concentration. Results of inhibitory effects of 6 chitosans on growth of Bacillus sp. (S08) failed to detect viable cells after incubation for 24 hrs at 37 C, even at 0.02% concentration. With B. megaterium (S10) and B. cereus (S27), a 3 to 4 log cycle reduction was found in the chitosan‐treated group. The growth of Enterobacter sakazakii (S35) was completely suppressed in the presence of 0.04% chitosan except for 1 chitosan product. The minimum inhibitory concentration of chitosan differed with products and isolates, ranging from 0.005% to above 0.1%.     

Physicochemical,Microstructural, and Antibacterial Properties of β‐Chitosan and Kudzu Starch Composite Films

Abstract: This study investigated physicochemical, microstructural, and antibacterial properties of β‐chitosan–kudzu starch composite films with addition of 0%, 20%, 60%, or 100% kudzu starch (w starch/w chitosan) in 1% chitosan solution. Molecular interactions between chitosan and kudzu starch and the crystal structure of the films were also determined. Adding 60% kudzu starch reduced water vapor permeability and solubility of pure β‐chitosan film by about 15% and 20%, respectively, whereas mechanical strength and flexibility of the film were increased about 50% and 25%, respectively. Micrograph showed that β‐chitosan film was totally amorphous, and the composite films generally became rougher with more starch added. Fourier transform infrared and X‐ray diffraction spectra showed that the 2 film‐forming components were compatible with each other. Pure β‐chitosan film resulted in 9.5 and 11.5 log CFU/mL reduction in Escherichia coli and Listeria innocua based on plate count method, respectively. Addition of kudzu starch reduced the antibacterial activity of film, but still achieved 8.3 and 10.3 log CFU/mL reduction in E. coli and L. innocua, respectively when kudzu starch to chitosan weight ratio was 1:1. Reduced antibacterial activity might attribute to the interaction of amino groups in β‐chitosan with the hydroxyl groups in kudzu starch. This study demonstrated that kudzu starch effectively improved water barrier of β‐chitosan film, and the composite films retained strong antibacterial ability. Practical Application: One percent of β‐chitosan containing 60% kudzu starch (w/w chitosan) composite films possessed better mechanical and water barrier properties than pure β‐chitosan films, and showed strong antibacterial activity against both Gram‐positive and Gram‐negative bacteria. The films may be used as wraps or coatings to prolong the shelf life of different foods or other similar applications.     

几种壳聚糖的抑菌性能

通过壳聚糖的抑菌实验和几种壳聚糖的最低抑菌浓度的测定 ,比较了相同脱乙酰度不同分子量 ,以及分子量相近脱乙酰度不同的壳聚糖对金黄色葡萄球菌、枯草杆菌、大肠杆菌和假单胞菌的抑菌作用。结果表明 ,实验中用到的壳聚糖都对金黄色葡萄球菌有很强的抑菌作用 (抑菌率接近 10 0 % ,最低抑菌浓度为 0 0 3% ) ;对于其他 3种细菌 ,脱乙酰度相同 (为 75 3%或 93 7% ) ,粘均分子量不同 (在 4 0～ 80万之间 )的壳聚糖 ,抑菌作用随分子量的升高而增强 ;而分子量相近脱乙酰度不同的壳聚糖对上述 4种细菌的抑菌作用差别不大 ;在 pH 5 5左右至 pH 6 0左右壳聚糖能够发挥最强的抑菌作用 ;总体看来 ,壳聚糖对金黄色葡萄球菌的抑菌作用最强 ,其次是对假单胞菌和枯草杆菌 ,壳聚糖对大肠杆菌的抑菌作用相对弱一些 ;实验条件下的壳聚糖对上述 4种细菌的抑菌作用普遍比苯甲酸钠强。     

Physicochemical and functional properties of chitosans affected by sun drying time during decoloration

The typical production of chitosan from crustacean shell consists of demineralization, deproteinization, decoloration, and deacetylation. Selected physicochemical and functional properties of chitosans as affected by various decoloration times (4, 5, 6, 7 or 8 h) using sun drying were evaluated. Moisture content (6.67-6.89 g/100 g), degree of deacetylation (81.91-82.73%), and color L^∗ value (78.32-79.43) of chitosans were not affected by sun drying time. However, color a^∗ and b^∗ values decreased when sun drying time was over 4 h. The viscosity of chitosan solution (0.5 g/100 mL acetic acid) decreased gradually with increasing sun drying time, with a more pronounced effect observed at 8 h of sun drying. There was no change in water-binding capacity (WBC) of chitosans decolorized by sun drying between 4 and 6 h; however, further increase in sun drying time from 6 to 7 or 8 h increased WBC of chitosans. DPPH radical scavenging activity of chitosans increased with increasing sun drying time. This study demonstrated that white-colored chitosans could be produced by an alternative decoloration step using sun drying for 4 h following the deacetylation step. However, increasing sun drying time to 7 h produced chitosan with increased WBC and DPPH radical scavenging activity.     

Antifungal activity of chitosan and its application to control post‐harvest quality and fungal rotting of Tankan citrus fruit (Citrus tankan Hayata)

In this study, the antifungal activity of chitosan A (MW = 92.1 kDa) and B (MW = 357.3 kDa), with 94.2% N‐deacetylation were examined at various concentrations against fungi including Penicillium digitatum, Penicillium italicum, Botrydiplodia lecanidion and Botrytis cinerea. The effectiveness of these chitosans to control the post‐harvest quality of Tankan fruit, a popular sub‐tropical citrus fruit, was investigated. It was found that chitosan, depending on type and concentration, caused 25.0–90.5% growth inhibition on test organisms after 5 days of cultivation at 24 °C. Chitosan treatment significantly reduced (P < 0.05) the percentage decay of Tankan fruit during storage at 24 °C. After 42 days of storage at 13 °C, chitosan‐coated Tankan fruits were firmer, exhibited less decay and weight loss, and showed higher titratable acidity, ascorbic acid, and total soluble solids than the control fruit. Weight loss of Tankan fruits decreased as the concentration of chitosan was increased. On the other hand, chitosan A, regardless of concentration tested, was found to be more effective in retaining the firmness, titratable acidity and water content, total solid content and ascorbic acid content of Tankan fruits than chitosan B. Copyright © 2006 Society of Chemical Industry     

A comparative study on the polyphenolic content,antibacterial activity and antioxidant capacity of different solvent extracts of Brassica oleracea vegetables

Brassica vegetables are rich in polyphenols, flavonoids and glucosinolates. Investigation was undertaken to optimise the best solvents among 60% ethanol, acetone and methanol for the extraction of polyphenols from Brassica vegetables. Furthermore, different properties such as antibacterial activity and antioxidant capacity were also investigated. Results showed that a 60% methanolic extract showed the highest total phenolic content which was 23.6, 20.4 and 18.7 mg gallic acid equivalents (GAE) g^?1 extract for broccoli, Brussels sprouts and white cabbage, respectively. The hydroxybenzoic acid content of various solvent extracts ranged from 5.86 to 8.91 GAE g^?1 extract for broccoli, 2.70 to 5.44 GAE g^?1 extract for Brussels sprouts and 3.69 to 4.86 GAE g^?1 extract for white cabbage, while the hydroxycinnamic acid content ranged from 0.78 to 1.26 chlorogenic acid equivalents (CAE) g^?1 extract for broccoli, 1.41 to 3.45 CAE g^?1 extract for Brussels sprouts and 0.49 to 1.14 CAE g^?1 extract for white cabbage. A concentration‐dependent antioxidative capacity was confirmed for different reactive oxygen species, and moderate antibacterial activity was observed against a number of Gram‐negative and Gram‐positive food spoilage and food pathogenic bacteria. Solvents significantly affected polyphenolic content and its different properties, and the methanol was found to be the best solvent for the extraction of polyphenols from studied Brassica vegetables.     

Evaluation Antibacterial Activity of Quaternary‐Based Chitin/Chitosan Derivatives In Vitro

Abstract: Total of 3 water‐soluble quaternary‐based chitin/chitosan derivatives, which have an identical molecular weight and anion, were synthesized and characterized. Their antibacterial activities against Salmonella cholerae‐suis and Bacillus subtilis were evaluated in vitro. The polysaccharides exhibited the antibacterial efficiency. Their minimum inhibitory concentration (MIC) values vary from 0.02 to 20.48 mg/mL, and their minimum bactericidal concentration (MBC) values vary from 0.08 to 40.96 mg/mL against S. cholerae‐suis and B. subtilis, respectively. Futhermore, the extent of Bacillus subtilis cells damage was examined via transmission electron microscopy (TEM) to show how N,N,N‐trimethylchitosan (TMC) gradually destroyed and killed B. subtilis cells when they were treated with TMC. One of those quaternary polymers, O‐([2‐hydroxy‐3‐trimethylammonium])propyl chitin (OHT‐chitin), which can be directly and easily synthesized from chitin in bulk quantities, also was demonstrated its antibacterial activity. These water soluble quaternary‐based chitin/chitosan derivatives that have antibacterial effect should be potentially used as antimicrobial agents in many fields. Practical Application: The main practical application behind the investigation and evaluation antibacterial activity of 3 water‐soluble quaternary‐based chitin/chitosan derivatives could be potentially used as antimicrobial agents in many fields. These polysaccharides represent a renewable source of natural biodegradable polymers and meet with the emergence of more and more food safe problems.     

Use of chitosan for the removal of metal ion contaminants and proteins from water

Naturally abundant biosorbants such as chitin and chitosan are recognized as excellent metal ligands, forming stable complexes with many metal ions, and serving as effective protein coagulating agents. Chitin isolated from crab processing discards was deacetylated over different time periods in order to obtain three types of chitosans [Type 1 (20 h), Type 2 (10 h) and Type3 (4 h)]. Chitosans so prepared were evaluated for their capacity to chelate metal ions in samples of water obtained from a zinc mining site (Buchans, Newfoundland). Metal chelation capacity of chitosan for wastewater was determined by inductively coupled plasma-mass spectrometry (ICP-MS) at three different pH (5, 6 and 7). Chitosan served as an effective coagulating agent in removing proteins from wastewater as well as for the removal of metal ions [Hg(II), Fe(II), Ni(II), Pb(II), Cu(II) and Zn(II)] from industrial wastewater, especially at pH 7, as measured by ICP-MS. Mercury was best chelated by all three types of chitosan under all pH conditions tested. In the protein flocculation study, Type 1 chitosan showed the best flocculation ability followed by Type 2 and Type 3 chitosans.     

Profile of antioxidant and antibacterial activities of different solvent extracts from Rabdosia rubescens

The objective of this work was to investigate the antioxidant and antibacterial activities of different extracts from Rabdosia rubescens and to further evaluate the antibacterial mechanism of extracts. The results showed that 80% acetone extracts had the highest contents of total polyphenols (8.09 mg GAE g^?1) and flavonoids (5.69 mg RE g^?1) and exhibited the strongest antioxidant activities, followed by 80% methanol and 80% ethanol, and the lowest for hexane extracts. Others except for hexane extracts showed different antibacterial activities against Gram‐positive strains, while no inhibitory effects were found on tested Gram‐negative bacterial strains. Among these extracts, 80% acetone and ethanol extracts had relatively higher antibacterial activities with the lowest minimum inhibitory concentration and minimum bactericidal concentration values of 5 and 10 mg mL^?1. The antibacterial mechanism of ethanol extracts against Staphylococcus aureus might be described as it disrupts cell wall, increases cell membrane permeability and then leads to the leakage of cell constituents.