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Gluco‐oligosaccharides (GlcOS) are potential prebiotics that positively modulate beneficial gut commensals like lactobacilli. For the rational design of GlcOS as prebiotics or combined with lactobacilli as synbiotics, it is important to establish the structure requirements of GlcOS and specificity toward lactobacilli. Herein, the utilization of 10 GlcOS with varied degrees of polymerization (DP) and glycosidic linkages by 7 lactobacilli strains (Levilactobacillus brevis ATCC 8287, Limosilactobacillus reuteri ATCC PTA 6475, Lacticaseibacillus rhamnosus ATCC 53103, Lentilactobacillus buchneri ATCC 4005, Limosilactobacillus fermentum FUA 3589, Lactiplantibacillus plantarum WCFS1, and Lactobacillus gasseri ATCC 33323) was studied. L. brevis ATCC 8287 was the only strain that grew on α/β‐(1→4/6) linked disaccharides, whereas other strains showed diverse patterns, dependent on the availability of genes encoding sugar transporters and catabolic enzymes. The effect of DP on GlcOS utilization was strain dependent. β‐(1→4) Linked cello‐oligosaccharides (COS) supported the growth of L. brevis ATCC 8287 and L. plantarum WCFS1, and shorter COS (DP 2–3) were preferentially utilized over longer COS (DP 4–7) (consumption ≥90% vs. 40%–60%). α‐(1→4) Linked maltotriose and maltodextrin (DP 2–11) were effectively utilized by L. brevis ATCC 8287, L. reuteri ATCC 6475, and L. plantarum WCFS1, but not L. fermentum FUA 3589. Growth of L. brevis ATCC 8287 on branched isomalto‐oligosaccharides (DP 2–6) suggested preferential consumption of DP 2–3, but no preference between α‐(1→6) and α‐(1→4) linkages. The knowledge of the structure‐specific GlcOS utilization by different lactobacilli from this study helps the structural rationale of GlcOS for prebiotic development. [ABSTRACT FROM AUTHOR]

Background: Evaluating the efficacy of letrozole overlapped with gonadotropin-modified letrozole protocol (mLP) for diminished ovarian reserve (DOR) or advanced-age women with repeated cycles. Methods: This is a retrospectively registered, paired-match study including 243 women with DOR and 249 women aged over 40 years old who received in vitro fertilization (IVF) treatment. 123 women received stimulation with mLP (mLP group). GnRH agonist (GnRH-a) long, GnRH antagonist (GnRH-anta), and mild stimulation protocol were used as controls with 123 women in each group. We further analyzed 50 of 123 patients in the mLP group who have experienced more than one failed cycles with other ovarian stimulation protocols (non-mLP group). Clinical pregnancy rate (CPR), cumulative clinical pregnancy rate (CCPR), and live birth rate (LBR) were main outcomes. Results: The CPR in the mLP group (38.46%) was significantly higher than mild stimulation (17.11%), but not significantly different from GnRH-a long (26.13%) and GnRH-anta (29.17%) group. The CCPR showed an increasing trend in the mLP group (33.33%) although without significance when compared with controls. The CCRP of GnRH-a long, GnRH-anta, mild stimulation group were 21.68%, 29.03%, and 13.04%, respectively. In women with repeated cycles, mLP achieved the higher available embryo rate (P < 0.05), the top-quality embryo rate, the CPR (P < 0.001), and the LBR (P < 0.001). Further study showed a positive correlation between testosterone and the number of oocytes retrieved in the mLP group (r = 0.395, P < 0.01). Conclusion: The mLP may be effective for aged or DOR women who have experienced previous cycle failure by improving the quality of embryos, the CPR, and the LBR. An increasing serum testosterone level may reflect follicular growth during ovarian stimulation. [ABSTRACT FROM AUTHOR]

Prebiotics have long been used to modulate the gut microbiota and improve host health. Most established prebiotics are nondigestible carbohydrates, especially short‐chain oligosaccharides. Recently, gluco‐oligosaccharides (GlcOS) with 2–10 glucose residues and one or more O‐glycosidic linkage(s) have been found to exert prebiotic potentials (not fully established prebiotics) because of their selective fermentation by beneficial gut bacteria. However, the prebiotic effects (non‐digestibility, selective fermentability, and potential health effects) of GlcOS are highly variable due to their complex structure originating from different synthesis processes. The relationship between GlcOS structure and their potential prebiotic effects has not been fully understood. To date, a comprehensive summary of the knowledge of GlcOS is still missing. Therefore, this review provides an overview of GlcOS as potential prebiotics, covering their synthesis, purification, structural characterization, and prebiotic effect evaluation. First, GlcOS with different structures are introduced. Then, the enzymatic and chemical processes for GlcOS synthesis are critically reviewed, including reaction mechanisms, substrates, catalysts, the structures of resultant GlcOS, and the synthetic performance (yield and selectivity). Industrial separation techniques for GlcOS purification and structural characterization methods are discussed in detail. Finally, in vitro and in vivo studies to evaluate the non‐digestibility, selective fermentability, and associated health effects of different GlcOS are extensively reviewed with a special focus on the GlcOS structure–function relationship. [ABSTRACT FROM AUTHOR]

Solid acids as heterogeneous catalysts for cellulose hydrolysis have drawn increasing attention; however, current solid acids face challenges such as high catalyst loading (low catalytic activity), poor catalyst-substrate interaction, deficient hydrothermal stability, and unsatisfactory recyclability. This review critically discussed the recent efforts and progress in overcoming the issues of solid acids and developing high-performance solid acids for hydrolyzing cellulose. The key structural features of solid acids and their effects on the interactions with cellulose and cellulose hydrolysis were addressed in detail. Strategies and perspectives to enhance performance, hydrothermal stability and recyclability of solid acids were provided. [ABSTRACT FROM AUTHOR]

A linear pH-responsive zwitterionic copolymer P(MDB) was synthesized from functional monomers methacrylic acid, 2-(dimethylamino) ethyl methacrylate (DMA) and benzyl methacrylate (BMA) through free radical polymerization to recover cellulases and enhance the enzymatic hydrolysis. The hydrophobicity and molecular weight of the copolymer was controlled by the feed ratio of monomers and the mass ratio of initiator to monomers, respectively. UV-turbidity showed P(MDB) exhibited sensitive pH-responsiveness with dissolution–precipitation ΔpH about 1 pH unit. The precipitation pHφ of P(MDB) was 5.0–5.5 and over 90% of P(MDB) could precipitate in the vicinity of its isoelectric point. Increasing the hydrophobicity or molecular weight of P(MDB) could improve its pH sensitivity and precipitation rate. P(MDB) could enhance the enzymatic hydrolysis of dilute acid pretreated Eucalyptus by 10–25%. P(MDB) could recover the free cellulases in enzymatic hydrolysate by co-precipitation. SDS-PAGE analysis showed that P(MDB) could recover 100% β-glucosidase (β-GL) and the recovery rates of cellobiohydrolase (CBH) and endoglucanase (EG) increased as the hydrophobicity and molecular weight of P(MDB) increased. The mechanism was proposed that hydrophobic affiliation was the main binding force of P(MDB) to cellulases. Increasing the hydrophobicity and molecular weight of copolymer could increase its binding force and the number of binding sites to cellulases thus the overall cellulase recovery performance was improved. [ABSTRACT FROM AUTHOR]

Sulfonation degree is an important structural parameter of lignosulfonates which affect their water solubility, surface activity, and dispersing performance. Presently, the methods for determining sulfonation degree include elemental analysis and potentiometric titration; they have some shortcomings such as complex purification process, high equipment requirements, and time-consuming. Hence, a simple and rapid method to determine the sulfonation degree of lignosulfonates was proposed based on the electrostatic interaction between cationic surfactant (hexadecyl trimethyl ammonium bromide (CTAB)) and anionic lignosulfonates. CTAB was added and co-precipitated with lignosulfonates and then the ultraviolet absorbance of the supernatant was determined. The sulfonation degree of lignosulfonates was calculated according to the titration curve of the supernatant absorbance to the amount of CTAB. This method is applicable to lignosulfonates recovered from acid pulping as well as sulfonation products of alkali lignin. Because of the easy operation process and no purification process for lignosulfonates, this method was simple and rapid when compared to existing methods for sulfonation degree determination of lignosulfonates. [ABSTRACT FROM AUTHOR]

Effect of hydrogen bond breaker (urea) addition on the enzymatic hydrolysis of Avicel and eucalyptus pretreated by dilute acid (Eu-DA) was investigated. Urea enhanced the enzymatic hydrolysis of Eu-DA at 50 or 30 °C when the concentration of urea was below 60 g/L, while it inhibited the hydrolysis of Avicel. Low concentration urea (< 240 g/L) had little effect on the cellulase spatial structure and its activity. But it decreased cellulase binding to cellulose surface to inhibit the cellulose hydrolysis. Meanwhile, urea obviously prevented the adsorption of cellobiohydrolase I (CBHI) on the lignin in spite of little effect on the adsorption of β-glucosidase (BGL) and two endoglucanases (EGIII and EGV) on lignin. It was proposed that urea enhanced the enzymatic efficiency of Eu-DA by decreasing the cellulase adsorption on lignin surface. [ABSTRACT FROM AUTHOR]

In order to enhance the enzymatic hydrolysis of lignocelluloses and recycle surfactants after enzymatic hydrolysis, a pH-responsive lignin amphoteric surfactant (SLQA) was prepared by the quaternization of sulfonated lignin (SL). Compared with SL, SLQA could much more effectively enhance the enzymatic hydrolysis of lignocelluloses. With an increase in the quaternization degree, enhancement of the enzymatic hydrolysis of lignocelluloses by the SLQA gradually increased. Adding 2 g L−1 SLQA-80 (mass radio of quaternizing agent to SL was 80%) could increase the enzymatic digestibility of pretreated eucalyptus and corncob residues (CCR) from 36.7% and 37.8% to 84.3% and 90.5%, respectively. The adsorption of SLQA on lignin film was larger than that of SL, and the lignin film became more hydrophilic after adsorbing SLQA. Thus, SLQA could cause more effective steric hindrance and form a hydration layer to reduce the non-productive adsorption of cellulase on lignin. The purified SLQA-80 exhibited sensitive pH-responsive property, and 90.8% of SLQA-80 could be recycled by adjusting the pH of hydrolysate after enzymatic hydrolysis. Adding recyclable SLQA could not only obviously enhance the enzymatic hydrolysis of lignocelluloses, but could also enable the comprehensive utilization of lignocelluloses. This method is of great significance to reducing the cost of cellulosic ethanol. [ABSTRACT FROM AUTHOR]