Enhanced nutrient removal and facilitating granulation via intermittent aeration in simultaneous partial nitrification endogenous denitrification and phosphorus removal (SPNEDpr) process.

A novel simultaneous partial nitrification, endogenous denitrification and phosphorus removal (SPNEDpr) system was operated for 213 days in a sequencing batch reactor to treat real domestic sewage. The nutrient removal was achieved under an operation mode of intermittent aeration at unequal intervals with low oxygen concentrations. Through optimizing intermittent aeration conditions, the removal efficiencies of total inorganic nitrogen (TIN), PO43-P and chemical oxygen demand (COD) reached 78.40%, 98.13% and 84%, respectively. Low-oxygen (0.1-0.7 mg/L) and intermittent aeration effectively inhibited nitrite oxidation bacteria (NOB), maintaining stable partial nitrification with nitrite accumulation ratio of 96.45%. Notably, intermittent aeration promoted the formation of aerobic granular sludge, with the sludge particle size increasing from 217.2 ± 5.3 to 351.8 ± 4.8 µm, thereby enhancing the TIN loss efficiency (81.3%). The predominant genus was Candidatus_Competibacter (11.6%), which stored COD as intracellular carbon source and performed the endogenous denitrification. The SPNEDpr process provided a highly efficient and economical method for treating urban sewage.

Authentication of the Bilberry Extracts by an HPLC Fingerprint Method Combining Reference Standard Extracts.

A simple and fast high-performance liquid chromatography (HPLC) fingerprint method combining reference standard extract for the identification of bilberry extract was developed and validated. Six batches of bilberry extract collected from different manufactures were used to establish the HPLC fingerprint. Other berry extracts-such as blueberry extracts, mulberry extracts, cranberry extracts, and black rice extracts-were also analyzed for their HPLC chromatograms. The fingerprints of five batches of bilberry extract showed high similarities, while one batch was distinguished from others. Additionally, the content of anthocyanin Cyanidin-3-O-glucoside (Cy-3-glc) in each berry extract was analyzed and compared. The results indicate that this HPLC fingerprint method, combining reference standard extracts, could be used for the authentication and quality control of bilberry extracts.

Nutrient removal and microbial community in a two-stage process: Simultaneous enhanced biological phosphorus removal and semi-nitritation (EBPR-SN) followed by anammox.

This study developed a two-stage process, including simultaneous enhanced biological phosphorus-removal and semi-nitritation (EBPR-SN) sequencing batch reactor (SBR), followed by Anammox SBR, to achieve advanced nitrogen (N) and phosphorus (P) removal from real sewage with low carbon/nitrogen (2.82). The long-term operation suggested that removal efficiencies for TIN (86.2 ± 3.5%) and P (95.0 ± 5.5%) were stably obtained, with nitrite accumulation ratio of 98.7% in EBPR-SN SBR. Mechanism analysis indicated contribution of anammox to N-removal being 57.3%-73.7% and superior P-removal due to the majority of removed organics (~74.5%) being stored by polyphosphate-accumulating organisms (PAOs). In EBPR-SN SBR, high-throughput sequencing showed ammonium-oxidizing bacteria was 0.03% while nitrite-oxidizing bacteria was not detected, and PAOs accounted for 30.07%. In Anammox SBR, Candidatus Brocadia (9.75%) was the only anammox bacteria. Remarkably, short aerobic hydraulic retention time (4.29 h) with low DO (0.3-1.2 mg/L) during the whole process provided desirable energy-saving.

Enhanced nutrient removal of simultaneous partial nitrification, denitrification and phosphorus removal (SPNDPR) in a single-stage anaerobic/micro-aerobic sequencing batch reactor for treating real sewage with low carbon/nitrogen.

The feasibility of simultaneous partial nitrification, denitrification and phosphorus removal (SPNDPR) process was investigated in a single-stage anaerobic/micro-aerobic sequencing batch reactor for treating real sewage. Partial nitrification was maintained with average nitrite accumulation ratio of 90.3% during 266 days' operation. Removal efficiencies for NH4+-N (96.3%), total inorganic nitrogen (81.4%), and phosphorus (91.0%) were stably obtained when treated real sewage with low carbon/nitrogen (3.4), with simultaneous partial nitrification and denitrification efficiency of 73.1%. The mechanism analysis revealed that denitrifying glycogen-accumulating organisms (DGAOs) and denitrifying polyphosphate-accumulating organisms (DPAOs) played the main roles in N-removal and P-removal, respectively. Nitrite pathway and optimized use of the organic carbon available in the sewage were keys for the successful performance. Further microbial community illustrating that DGAOs Candidatus_Competibacter, DPAOs Dechloromonas, and ammonia-oxidizing bacteria Nitrosomonadaceae were main functional groups. Notably, sludge granulation was formed under long-term synchronous low dissolved oxygen and low sludge loading conditions, avoiding sludge bulking.

[Analysis of lipophilic components of Salvia miltiorrhiza roots and S. yunnanensis roots by UPLC and LC-MS/MS].

Fingerprints of lipophilic components in the roots of Salvia miltiorrhiza and S.yunnanensis were analyzed by UPLC-DADand UPLC coupled with mass spectroscopy to evaluate the differences and similarities of the lipophilic components in the two kinds of herbs.The UPLC analysis of 18 batches of S.miltiorrhiza and 16 batches of S.yunnanensis was performed on a 25℃Thermo Accucore C_(18)column(2.1 mm×100 mm,2.6µm)by Shimadzu LC-20AD;mobile phase was 0.026%phosphoric acid(A)-acetonitrile(B)with gradient elution;flow rate was 0.4 m L·min~(-1);detection wavelength was set at 270 nm;injection volume was 2µL.The molecular structures of the lipophilic components were analyzed on a 25℃Thermo Accucore C_(18)column(2.1 mm×100 mm,2.6µm)by Thermo U3000 UPLC Q Exactive Orbitrap LC-MS/MS with a mobile phaseconsisting of 0.1%formic acid water(A)and 0.1%formic acidacetonitrile(B).The mass spectrometry was acquired in positive modes using ESI.There are 10 common peaks in the lipophilic components of S.miltiorrhiza.The similarity between the 16 batches of S.miltiorrhiza and their own reference spectra was greater than 0.942,and the average similarity was 0.973.There are 12 common peaks in the lipophilic components of S.yunnanensis.The similarity between the 18 batches of S.yunnanensis and their own reference spectra was greater than 0.937,and the average similarity was 0.976.The similarity between the reference chromatograms of S.miltiorrhiza and S.yunnanensis was only 0.900.There are three lipophilic components in S.yunnanensis,which are not found in S.miltiorrhiza,and one of which isα-lapachone.There is a lipophilic component in S.miltiorrhiza not found in S.yunnanensis,which may be miltirone.The two herbs contain 8 common lipophilic components including dihydrotanshinoneⅠ,cryptotanshinone,tanshinoneⅠ,tanshinoneⅡ_A,nortanshinone in which the content of tanshinoneⅡ_A,dihydrotanshinoneⅠand cryptotanshinone of S.yunnanensisis significantly lower than that of S.miltiorrhiza(P<0.01),and the contents of tanshinoneⅠand nortanshinone are significantly lower than that of S.miltiorrhiza too(P<0.05).There are significant differences in the types and contents of lipophilic components between the roots of S.miltiorrhiza and S.yunnanensis,and the similarity between the fingerprints of interspecies is much lower than that between the same species.Therefore,the roots of S.miltiorrhiza and S.yunnanensis are two kinds of herbs which are quite different in chemical compounds and compositions.

[Chemical constituents from Corydalis yanhusuo].

OBJECTIVE: To study the chemical constituents from the 60% ethanol extract of Corydalis yanhusuo. METHOD: The chemical constituents were separated and purified by various chromatographic techniques, and their structures were elucidated by chemical evidence and spectroscopic analysis. RESULT: Nine alkaloids were obtained and determined as 7-formyldidehydroglaucine (1), nantenine (2), (+)-O-methylbulbocapnine (3), d-corydaline (4), tetrahydrocoptisine (5), 8-oxocoptisine (6), palmatine (7), tetrahydropalmatine (8), and dehydrocorydaline (9), respectively. CONCLUSION: Compound 1 was obtained from natural products for the first time, and its NMR data were firstly reported. Compound 3 was reported from Papaveraceae for the first time, and compound 6 was firstly reported from Corydalis yanhusuo.