Accumulation of lankamycin derivative with a branched-chain sugar from a blocked mutant of chalcose biosynthesis in Streptomyces rochei 7434AN4.

Lankamycin, a macrolide antibiotic produced by Streptomyces rochei 7434AN4, exhibits a moderate antimicrobial activity and acts as a synergistic pair with carbocyclic antibiotic lankacidin C by binding to the ribosome exit tunnel. Its biosynthetic gene (lkm) cluster (orf24-orf53) is located on the largest plasmid pSLA2-L (210,614 bp). Our group possesses a variety of lankamycin derivatives and macrolide-modification enzymes including P450 enzymes and glycosyltransferases, which may lead to expand the chemical library of bioactive macrolides. Here we constructed a mutant of a 3-ketoreductase gene lkmCVI (orf42) involved in d-chalcose biosynthesis, and its metabolite was isolated and structure-elucidated. Accumulation of novel lankamycin derivative harboring a branched-chain deoxysugar, 5-O-(4',6'-dideoxy-3'-C-acetyl-d-ribo-hexopyranosyl)-3-O-(4″-O-acetyl-l-arcanosyl)-lankanolide, indicated that LkmCVI acts as a gate keeper enzyme for d-chalcose synthesis in lankamycin biosynthesis.

Phosphate removal from aqueous solution using calcium-rich biochar prepared by the pyrolysis of crab shells.

Phosphorus is one of the main pollutants that cause water pollution, and phosphorus is a one-way cycle in the environment, and phosphorus resources will face exhaustion in the next 100 years. Therefore, the recovery and reuse of phosphorus resources have become very important. This article presents a study concerning the removal of phosphate from an aqueous solution by using a calcium-rich biochar prepared by pyrolysis of crab shells. The experimental results show that the optimal pyrolysis temperature of crab shells is 500 â„ƒ, named CSB500, which is more conducive to the adsorption of phosphate. The process of phosphate adsorption conforms to the quasi-second-order kinetics and Freundlich model. On the other hand, the Langmuir isotherm model shows that when the reaction conditions are 25 â„ƒ, 30 â„ƒ, and 35 â„ƒ, the maximum adsorption capacity of CSB500 for phosphate is 164.32 mg/g, 170.47 mg/g, and 209.35 mg/g, respectively. The characterization results show that the overall structure of CSB500 is good, the specific surface area is large, and the main component is calcium carbonate. The potential mechanisms of action in the process of phosphate adsorption may be electrostatic attraction, surface chemical precipitation, ligand exchange, and complexation.

Investigation into lanthanum-coated biochar obtained from urban dewatered sewage sludge for enhanced phosphate adsorption.

Phosphate adsorption using metal-modified biochar has awakened much attention and triggered extensive research. In this study, the effect of lanthanum (La)-modified sludge using impregnation-co-precipitation was used for phosphate adsorption. Consequently, La-coated biochar at a pyrolysis temperature of 600 °C had the highest phosphate adsorption and the lowest heavy metal leaching potential. The treatment of virgin biochar with alkali before La loading was found to be beneficial for the increase of phosphate adsorption capacity. The adsorption kinetics was well depicted by the pseudo-second-order model, and indicating that intraparticle diffusion played a crucial role in the adsorption process. The good fitness between adsorption data and the Langmuir isotherm model showed a maximal adsorption capacity of 93.91 mg/g, where phosphate absorption was highly correlated to its concentration in the solution. The La-coated biochar showed high adsorption capacity when the solution pH varied from 3.0 to 6.0, and was insensitive to the coexisting chloride, nitrate, sulfate, bicarbonate and citrate. Moreover, the adsorption mechanism was further explored by using Zeta potential analysis, FTIR and XPS, indicating that the phosphate is adsorbed through electrostatic attraction in the form of the inner-sphere complexation. All the results suggested that the sludge-based biochar, as a support material for La, could serve as a promising adsorbent for phosphate in real applications.

Study on Hydrogen Sensitivity of Ziegler⁻Natta Catalysts with Novel Cycloalkoxy Silane Compounds as External Electron Donor.

Two novel cycloalkoxy silane compounds (ED1 and ED2) were synthesized and used as the external electron donors (EEDs) in Ziegler⁻Natta catalysts with diethyl 2,3-diisopropylsuccinate as internal electron donor. The results indicated that the Ziegler⁻Natta catalysts using ED1 and ED2 as EEDs had high catalytic activities and good stereoselectivities. The melt flow rate (MFR) and gel permeation chromatography (GPC) results revealed that the obtained polypropylene has higher MFR and lower average molecular weights than the commercial EED cyclohexyl methyl dimethoxysilane. The differential scanning calorimetry (DSC) results indicated that new isospecific active centers formed after the introduction of new external donors. The work implied that the novel EEDs could improve the hydrogen sensitivities of the catalyst system and obtain polymers with high melt flow rate.