Overview of bio nanofabric from bacterial cellulose

Nanofibers and bio-nonwoven fabrics of pure cellulose can be made from some bacteria such as Acetobacter xylinum. Bacterial cellulose fibers are very pure, 10?nm in diameter and about 0.5?micron long. The molecular formula of bacterial cellulose is similar to that of plant cellulose. Its fibers are very stiff and it has high tensile strength, high porosity, and nanofibrillar structure. They can potentially be produced in industrial quantities at greatly lowered cost and water content, and with triple the yield by a new process. This article presents a critical review of the available information on bacterial cellulose as a biological nonwoven fabric with special emphasis on its fermentative production and applications. Characteristics of bacterial cellulose biofabric with respect to its structure and physicochemical properties are discussed. Current and potential applications of bacterial cellulose in textile, nonwoven cloth, paper, films, synthetic fiber coating, food, pharmaceutical, and other industries are also presented.     

Comparative evaluation of bacterial cellulose (nata) as a cryoprotectant and carrier support during the freeze drying process of probiotic lactic acid bacteria

Nata or bacterial cellulose produced by Acetobacter xylinum was compared for its cryoprotective and carrier support potential for probiotic lactic acid bacteria against other established cryoprotectants like 10% skim milk, calcium alginate encapsulation or 0.85% physiological saline and distilled water. Individual lactic acid bacteria were grown in MRS broth in the presence of nata cubes or the bacterial suspension mixed with either powdered bacterial cellulose (PBC), 10% skim milk, saline or distilled water and freeze dried. These freeze dried cells were stored at temperatures of either 30 °C or 4 °C and periodically checked for viability. The freeze dried cells on carrier supports were directly used to prepare fermented milks to establish the activity of these cultures. Scanning electron microscopy was employed to visualize the support matrix with the attached lactic acid bacteria. The freeze drying process resulted in a 3.0 log cycle reduction in the colony forming units as compared to the original cell suspension in the case of all the lactic acid bacteria. The growth of lactic acid bacteria in the presence of bacterial cellulose (nata) offers a convenient and easy method to preserve bacteria for short durations and use it as a support to carry out other fermentation processes.     

Production of bacterial cellulose fibers in the presence of effective microorganism

In this study, effective microorganism (EM) was added into fermentation medium in static culture to enhance bacterial cellulose (BC) production by Acetobacter xylinum 23769 strain. According to SEM micrographs, BC pellicles from BC-Baikal EM1 show a smaller diameter and a relatively narrow diameter distribution compared to BC pellicles from Hestrin–Schramm (HS) medium. The BC-HS absorbed 90.5 times its dry weight of water. The water holding capacity increased to 132.5 for BC-Baikal EM1 medium compared to BC-HS. From the FT-IR spectra, BC samples exhibited a similar pattern. The crystalline indices of Baikal EM1-altered BC (66%) were lower than Baikal EM1-free BC (71%).     

Characteristics of thin‐layer drying and rehydration of nata de coco

Nata is white gelatinous bacterial cellulose produced by Acetobacter aceti ssp. xylinum through fermentation of coconut water. Drying behaviour of nata de coco was conducted with a hot air dryer for a temperature range of 50–90 °C. The experimental data obtained were fitted into seven empirical and/or semi‐theoretical thin‐layer drying models using nonlinear regression analysis. Results showed that Logarithmic model, Wang and Singh model fitted better than Verma et al. model although all these three models were suitable for predicting the drying process of nata de coco. The rehydration capacity was lost severely when the moisture content of the samples was nearly zero, but it can almost rehydrate to its initial state when the moisture content was above 8%. The drying kinetic properties and rehydration capacity of nata de coco indicated that most of the moisture in nata de coco was free water.     

Ultraviolet Treatment of Orange Juice to Inactivate <Emphasis Type="Italic">E. coli</Emphasis> O157:H7 as Affected by Native Microflora

The effect of yeast concentration on ultraviolet (UV) inactivation of five strains of Escherichia coli O157:H7 from different sources, inoculated both individually and simultaneously in orange juice, was analyzed and mathematically modeled. The presence of yeast cells in orange juice decreases the performance of UV radiation on E. coli inactivation. UV absorption coefficients in the juice increased with increasing yeast concentration, and higher UV doses were necessary to inactivate bacterial strains. UV intensities of I = 3.00 ± 0.3 mW/cm² and exposure times (t) between 0 and 10 min were applied; radiation doses (energy, E = I × t) ranging between 0 and 2 J/cm² were measured using a UV digital radiometer. All the tested individual strains showed higher resistance to the treatment when UV radiation was applied at 4 °C in comparison to 20 °C. UV inactivation of E. coli O157:H7 individual strain was satisfactory fitted with a first order kinetic model. A linear relationship was found between UV absorptivities and D values (radiation doses required to decrease microbial population by 90%) for each strain. The dose required to reach 5-log reduction for the most unfavorable conditions that is the most UV resistant strain, and maximum background yeast concentration was 2.19 J/cm² at 4 °C (corresponding to 11 min of UV treatment) and 2.09 J/cm² at 20 °C (corresponding to 10.55 min of UV treatment). When a cocktail of strains was inoculated in orange juice, the logistic equation was the best model that fits the experimental results due to the deviation from the log-linear kinetics. The UV resistance between strain cocktail and single strain were mathematically compared. Slopes of the decline curves for strain cocktail at high UV doses were lower than the slopes of the log-linear equation calculated for the individual strains, even for the most resistant one. Therefore, microbial inactivation tests using a cocktail of strains are particularly important to determine the performance of the UV inactivation treatment.     

Bacterial inactivation and quality changes of fresh‐cut avocados as affected by intense light pulses of specific spectra

Intense light pulses (ILP) treatments have good prospects for becoming an alternative to traditional thermal methods for decontamination of food surfaces. The aim of this work was to evaluate which ranges of the light spectrum are responsible for bacterial inactivation and their effect on the quality of fresh‐cut avocado. Results show that the effectiveness of ILP treatment decreases when the ultraviolet (UV) spectral region is blocked (particularly UV‐C). ILP treatments without UV‐C light (305–1100 nm) and an overall fluence of 10.68 J cm^?2 caused reductions of 2.47 and 1.35 log CFU g^?1 in the initial counts of inoculated Escherichia coli and Listeria innocua, respectively, in comparison with those treated using only VIS–NIR light (0.83 and 0.68 log CFU g^?1, respectively). Treatments applying light of a wavelength between 305 and 1100 nm had a more pronounced impact on colour, texture and headspace gas composition than treatments that did not contain UV light (400–1100 nm).     

Microbial Safety and Shelf Life of UV‐C Treated Freshly Squeezed White Grape Juice

The effects of UV‐C irradiation on the inactivation of Escherichia coli K‐12 (ATCC 25253), a surrogate of E. coli O157:H7, and on the shelf life of freshly squeezed turbid white grape juice (FSWGJ) were investigated. FSWGJ samples were processed at 0.90 mL/s for 32 min by circulating 8 times in an annular flow UV system. The UV exposure time was 244 s per cycle. The population of E. coli K‐12 was reduced by 5.34 log cycles after exposure to a total UV dosage of 9.92 J/cm² (1.24 J/cm² per cycle) at 0.90 mL/s flow rate. The microbial shelf life of UV‐C treated FSWGJ was extended up to 14 d at 4 °C. UV exposure was not found to alter pH, total soluble solid, and titratable acidity of juice. There was a significant effect (P < 0.05) on turbidity, absorbance coefficient, color, and ascorbic acid content. Furthermore, all physicochemical properties were altered during refrigerated storage. The microbial shelf life of FSWGJ was doubled after UV‐C treatment, whereas the quality of juice was adversely affected similarly observed in the control samples.     

Mutation of Acetobacter pasteurianus by UV irradiation under acidic stress for high‐acidity vinegar fermentation

To obtain a mutant with higher vinegar production, a wild‐type industrial strain Acetobacter pasteurianus CICIM B7003 was pretreated in 50 g L^?1 acetic acid for 1 h and cultured for 12 h without adding any acetic acid; then, the enriched cells were mutated by UV under acidic stress (60 g L^?1 acetic acid). Using this method, A. pasteurianus CICIM B7003‐02, a mutant exhibiting best performance, was obtained. Notably, after repeated experiments, it was confirmed that B7003‐02 accumulated 103.81 ± 1.17 g L^?1 acetic acid within 160‐h batch cultivation in Erlenmeyer flasks, which was 49.2% higher than that of the wild type. Repeated batch fermentations with A. pasteurianus B7003‐02 were carried out for several runs in a Frings 8‐L acetator, and high‐acidity vinegars (90 ± 0.39 g L^?1) were produced. This work reveals the potential value for improvement in industrial vinegar production.     

The biosynthesis of cellulose

To date, two basic cellulose synthesizing structures (TCs) have been described, the linear TC, typical of giant algae such as Boergesenia, Valonia and Eremosphaera and the rosette TC, characteristic of all vascular plants, ferns, mosses and certain algae such as Chara, Nitella and Moeugeotia. Linear terminal complexes are transported to the surface as subunits and later assembled into the linear structure. These linear structures continue to grow in length during microfibril assembly. The relationship of the TC structure to microfibril dimensions is discussed. Rosette TCs appear to be pre-assembled in the Golgi apparatus and transported to the surface intact. The topographical localization of TC structure in relation to patterns of microfibril deposition is described. The structure of the TC is discussed in relation to the synthesis of cellulose I and II. The biosynthesis of microbial cellulose by Acetobacter xylinum is summarized. Recent evidence for in vivo cellulose synthesis is given. The cellulose synthesizing complexes are located on the inner cytoplasmic membrane of Acetobacter and the regulatory proteins for controlling microfibril assembly may be located on the outer lipopolysaccharide membrane. Recent studies of in vitro synthesis indicated that cellulose II is made in vitro, whereas cellulose I is the more common allomorph produced in vivo.     

Effect of ultraviolet‐B irradiation on antioxidative properties of aqueous extracts from shiitake (Lentinus edodes) mushrooms

Antioxidant properties of aqueous extracts from Lentinus edodes treated with UV‐B irradiation were examined in vitro systems including DPPH, ABTS and oxygen radical absorbance capacity (ORAC) assays and in riboflavin‐photosensitised oil‐in‐water (O/W) emulsions. Changes in total phenolics, total flavonoids and vitamin C were also analysed. Lentinus edodes receiving 25 kJ m^?2 UV‐B treatment showed high radical scavenging ability based on DPPH and ABTS assays compared with samples with 0, 50 and 75 kJ m^?2, while those with 50 kJ m^?2 had higher antioxidant capacities than other samples from ORAC assays. Samples with 25 kJ m^?2 UV treatment had significantly 7.1% higher total phenolic content, 12.0% higher total flavonoid content and 8.0% higher vitamin C content than UV‐B‐untreated sample (P < 0.05), respectively. In O/W emulsions under riboflavin photosensitisation, 25 and 50 kJ m^?2 UV treatment significantly increased the oxidative stability compared with other samples based on headspace oxygen content and lipid hydroperoxide analyses (P < 0.05). Aqueous extracts of UV‐B‐treated mushrooms possessed enhanced antioxidant properties compared with untreated mushrooms.     

Chemometrics coupled with ultraviolet spectroscopy: a tool for the analysis of variety,adulteration, quality and ageing of apple juices

This study demonstrates the use of UV spectroscopy (UV) in combination with chemometrics as a simple and feasible approach for analysis of variety, adulteration, quality and ageing of apple juice. The results show that PCA‐UV is adequate to differentiate apple juice varieties and adulteration. The percentage of the adulterant can be detected by PLSR‐UV with RMSE < 0.7783% and R² > 0.9980. For the evaluation of juice quality, PLSR‐UV (RMSE = 0.2555–2.3448; R² = 0.7276–0.9816) is recommended for the prediction of soluble solids, ascorbic acid, total flavonoids, total sugar and reducing sugar, whilst PCR‐UV (RMSE = 0.0000–2.7426; R² = 0.7073–1.0000) is adequate for the prediction of pH and antioxidant activity. In addition, PLSR‐UV may be used to predict the storage time with RMSE = 0.4681 day and R² = 0.9832. Therefore, UV coupled with chemometrics has potential to be developed as a portable tool for the detection of variety, adulteration, quality and ageing of not only apple juices, but also other fruit and vegetable juices.     

UV inactivation of milk-related microorganisms with a novel electrodeless lamp apparatus

A novel UV apparatus based on Dean vortex technology is designed for inactivating bacteria in milk. In this apparatus, the milk flows through a helical quartz tube coiling around an electrodeless UV lamp (EUL) with a radio frequency of 2.65 MHz. Flow rate, inner diameter of quartz tube, different UV sources, and different types of bacteria have been found as the key factors for the valuable effects on bacterial inactivation. The EUL apparatus worked more efficiently in the UV inactivation of the predetermined populations of milk-related bacteria than the conventional low-pressure high-intensity mercury lamp. When the UV dose of 21.3 mJ/cm² was applied, the numbers of all the bacteria were reduced by more than 6 log₁₀ with a flow rate of 28.8 L/h and a tube’s inner diameter of 1.5 mm. Dean vortices were formed in the milk flow during the UV processing and played an important role in the UV inactivation of the bacteria. Another inactivation test with the apparatus applying the UV dose of 21.3 mJ/cm² was also done with raw cow’s milk containing indigenous microorganisms, including Salmonella and Shigella spp., Listeria monocytogenes, Staphylococcus spp., Enterobacteriaceae, lactic acid bacteria, pseudomonads, and the total aerobic bacteria were reduced by approximately 3–4 log₁₀. In short, the EUL apparatus requires smaller energy, occupies less space, and has simpler operating procedures than thermal pasteurization. Thus, the novel method provides a viable alternative to thermal pasteurization of milk for improving the microbial safety of milk and extending its shelf life.     

Construction of the mutant strain in Aspergillus oryzae 3.042 for abundant proteinase production by the N+ ion implantation mutagenesis

Because of secreting large amounts of enzymes, Aspergillus oryzae was widely used in the fermentation of soy sauce in many Asian countries. Here, N⁺ ion implantation mutagenesis was applied to improve the ability of A. oryzae to secrete acid protease. Several mutants were screened using three kinds of plates (Casein medium, Czapek’s medium and carboxymethyl cellulose medium agar plates). Compared with the other mutants, the mutant A100‐8 could secrete the most protease. Acid protease activity of A100‐8 was enhanced about 44.1% at 36 h by koji fermentation test. In addition, A100‐8 was stable by periodically subculturing and maintaining on the agar slant. The mRNA expression levels of two kinds of acid protease (serine carboxypeptidase and aspartyl protease) were measured by RT‐PCR at different periods. Serine carboxypeptidase and some kinds of aspartyl protease of A100‐8 were significantly (P < 0.01) expressed higher than the control at all times.     

Effect of ozonation on the rheological and colour characteristics of hydrocolloid dispersions

The effect of ozonation on the rheological and colour characteristics of guar, carboxyl methyl cellulose (CMC), and pectin dispersions was investigated. Guar 1%, CMC 1% and pectin 2% (w/v) dispersions were ozonated at varying ozone concentrations of 2.4%, 4.0%, 5.6% and 7.8% (w/w) for 3, 5, 7 and 10 min processing times at 20 ± 1.0 °C. Flow and dynamic rheological properties together with Hunter colour parameters (L^*, a^*, b^*) were measured for control and treated samples. Significant differences were observed in the rheological characteristics and colour of all ozonated hydrocolloid dispersion studied. No recovery was observed in the structure breakdown after a 24 h storage period. This study indicates that ozonation has a significant effect on both the rheology and colour of hydrocolloid dispersions and that due attention should be given before incorporating these hydrocolloids in food formulations which are subsequently ozonated in food processing and preservation processes.     

醇类对木醋杆菌JMCW-1合成细菌纤维素的影响

研究了不同醇类对木醋杆菌JMCW-1的影响。结果表明,不同醇类的添加对发酵液的pH影响不大;添加乙醇、丙三醇、乙二醇的发酵液中残糖含量均远远高于空白对照组,添加聚乙二醇的发酵液中残糖含量随添加量的增加先稍稍降低再升高随后又降低,添加聚乙烯醇的发酵液残糖含量随添加量的增加逐渐降低;添加乙二醇的发酵液OD值降低,添加其他5种醇的发酵液OD值升高;添加乙醇、丙三醇和聚乙烯醇可以提高细菌纤维素的产量,乙醇添加量为3.5%时,细菌纤维素的干质量最高,达到22.6 g/L,为未添加时的7倍;甲醇的添加对细菌纤维素的产量无明显影响。添加聚乙二醇、乙二醇对细菌纤维素的产量有一定的抑制作用。     

Potentially probiotic acetic acid bacteria isolation and identification from traditional dairies microbiota

Among probiotics, acetic acid bacteria (AAB) can be used as preservative agents because of their high fermentation and acidification activities. This study aimed to isolate, identify and biologically characterise Acetobacter strains from traditional Iranian dairy products. Acetobacter strains were identified by catalase assay, Gram staining, and combined repetitive sequence‐based PCR [(GTG)₅‐PCR fingerprints] and 16S rDNA gene sequencing. We identified eight strains belonging to four species, including Acetobacter aceti, Acetobacter indonesiensis, Acetobacter cibinongensis and Acetobacter syzygii. The molecular techniques could be used as an effective and rapid alternative tool to identify and characterise dairy‐associated AAB. Primary probiotic assessments, including low pH and high bile salt tolerance tests, antagonistic activity test against pathogens, and antibiotic susceptibility confirmed the probiotic properties of these AAB, particularly A. cibinongensis 34L strain, which was isolated from curd. Therefore, this strain can be introduced as novel candidate probiotics that could be used in the food industry.     

Relationship between growth of food‐spoilage yeast in high‐sugar environments and sensitivity to high‐intensity pulsed UV light irradiation

The relationship between prior growth of food‐spoilage yeast in high‐sugar environments and their subsequent survival postpulsed UV (PUV) irradiation was investigated. Test yeast were separately grown to early stationary phase in YPD broth containing increasing concentrations of glucose (1–50% w/v) and were flashed with ≤40 pulses of broad‐spectrum light at lamp discharge energy settings of 3.2, 7.2 and 12.8 J (equivalent to UV doses of 0.53, 1.09 and 3.36 μJ cm^?2, respectively) and their inactivation measured. Findings showed that prior growth in high‐sugar conditions (≥30% glucose w/v) enhanced the sensitivity of all nine representative strains of Zygosaccharomyces bailii, Z. rouxii and Saccharomyces cerevisiae yeast to PUV irradiation. Significant differences in inactivation amongst different yeast types also occurred depending on amount of UV dose applied, where the order of increasing sensitivity of osmotically stressed yeast to PUV irradiation was shown to be Z. rouxii, Z. bailii and >S. cerevisiae. For example, a 1.2‐log order difference in CFU mL^?1 reduction occurred between Z. bailii 11 486 and S. cerevisiae 834 when grown in 50% w/v sugar samples and treated with the uppermost test UV dosage of 3.36 μJ cm^?2, where these two yeast strains were reduced by 3.8 and 5.0 log orders, respectively, after this PUV treatment regime compared to untreated controls. The higher the UV dose applied the greater the reduction in yeast numbers. For example, a 1.0‐, 1.4‐ and 4.0‐log order differences in CFU mL^?1 numbers occurred for S. cerevisiae 834 grown in 15% w/v sugar samples and then treated with PUV dose of 0.53, 1.09 and 3.36 μJ cm^?2, respectively. These findings support the development of PUV for the treatment of high‐sugar foods that are prone to spoilage by osmotolerant yeast.     

细菌纤维素的生物合成及在食品工业的应用

细菌纤维素是经微生物发酵形成的新型生物合成材料,具有机械强度高、吸水性能好、纯度高、结晶度高等优良特性,广泛应用于食品工业等领域。已报道的产细菌纤维素的细菌有醋酸菌属(Acetobacter)、根瘤菌属(Rhizobium)、八叠球菌属(Sarcina)、土壤杆菌属(Agrobaeterium)、假单胞菌属(Preudomonas)、无色杆菌属(Achromobacter)、固氮菌属(Azotobacter)、气杆菌属(Aerobacter)和产碱菌属(Alcaligenes)这9个属中的某些种,真正能够应用于工业化生产细菌纤维素的只有醋酸菌中的几个种,他们是木醋杆菌(Acetobacter xylinum)、醋化醋杆菌(Acetobacteraceti)、产醋醋杆菌(Acetobacteracotigenum)和巴氏醋杆菌(Acetobacter pastcurianum)。本文通过分析近期国内外与细菌纤维素相关文献,对其高产菌种选育、培养基优化和发酵模式等方面的研究进行综述,并展望其在食品工业中的应用前景,为进一步深入研究细菌纤维素提供理论基础和科学依据。     

The Effect of Ultraviolet Light on Microbial Inactivation and Quality Attributes of Apple Juice

Non-thermal technologies such as UV irradiation can offer advantages for minimal processing of transparent beverages. In this study, reconstituted apple juice was exposed to UV light in a continuous laboratory scale system at energy dosages ranging from 2.66 to 53.10 J/cm² by changing the exposure time. Treated juices were then evaluated for microbial inactivation and selected physical and chemical attributes. Product quality was further assessed by sensory evaluation using a 30-member consumer panel. Microbiological analysis was performed by inoculating apple juice with Escherichia coli K12 and Listeria innocua and microbial numbers were counted pre- and post-processing. UV energy levels did not affect pH, °Brix, or total phenols content, but decreased non-enzymatic browning (p < 0.01) and antioxidant capacity (p < 0.05) compared to unprocessed juice. A colour-lightening effect was noted with increasing energy dose. All UV treatments applied (2.66 J/cm² and above) resulted in a reduction below the detection level (<1 log cfu/ml) for both E. coli and L. innocua in apple juice. Sensory evaluation showed that samples treated with energy dosages up to 10.62 J/cm² were comparable to the control in terms of acceptability, though higher dosages produced adverse effects in terms of flavour and colour. Based on these results, UV treatment with low energy dosages could represent a valid alternative to thermal processing to eliminate pathogenic microorganisms while maintaining quality in reconstituted apple juice.     

优化陈米糖化液提高细菌纤维素产量的研究

以木醋杆菌（Acetobacter xylinum）为发酵菌种,通过Plackett-Burman试验设计确定了陈米糖化液培养基中酵母膏、KH2PO4、FeSO4、乙醇对木醋杆菌发酵产细菌纤维素具有显著影响,并采用Box-Behnken试验设计对各显著影响因子进行优化,获得最优的陈米糖化液发酵培养基配方为：在陈米糖化液培养基基料中加入酵母膏13.1 g/L、蛋白胨10 g/L、KH2PO4 5.7 g/L、MgSO4 3.1 g/L、FeSO4 0.3 g/L、柠檬酸0.3 g/L、无水乙醇4.0%。在此优化条件下,细菌纤维素的产量为7.08 g/L,是陈米糖化液培养基基料发酵产细菌纤维素（0.38 g/L）的18.6倍,比基础发酵培养基细菌纤维素产量（4.80 g/L）提高了47.5%。