Discovery of Nuclear-Encoded Genes for the Neurotoxin Saxitoxin in Dinoflagellates

Saxitoxin is a potent neurotoxin that occurs in aquatic environments worldwide. Ingestion of vector species can lead to paralytic shellfish poisoning, a severe human illness that may lead to paralysis and death. In freshwaters, the toxin is produced by prokaryotic cyanobacteria; in marine waters, it is associated with eukaryotic dinoflagellates. However, several studies suggest that saxitoxin is not produced by dinoflagellates themselves, but by co-cultured bacteria. Here, we show that genes required for saxitoxin synthesis are encoded in the nuclear genomes of dinoflagellates. We sequenced >1.2×106 mRNA transcripts from the two saxitoxin-producing dinoflagellate strains Alexandrium fundyense CCMP1719 and A. minutum CCMP113 using high-throughput sequencing technology. In addition, we used in silico transcriptome analyses, RACE, qPCR and conventional PCR coupled with Sanger sequencing. These approaches successfully identified genes required for saxitoxin-synthesis in the two transcriptomes. We focused on sxtA, the unique starting gene of saxitoxin synthesis, and show that the dinoflagellate transcripts of sxtA have the same domain structure as the cyanobacterial sxtA genes. But, in contrast to the bacterial homologs, the dinoflagellate transcripts are monocistronic, have a higher GC content, occur in multiple copies, contain typical dinoflagellate spliced-leader sequences and eukaryotic polyA-tails. Further, we investigated 28 saxitoxin-producing and non-producing dinoflagellate strains from six different genera for the presence of genomic sxtA homologs. Our results show very good agreement between the presence of sxtA and saxitoxin-synthesis, except in three strains of A. tamarense, for which we amplified sxtA, but did not detect the toxin. Our work opens for possibilities to develop molecular tools to detect saxitoxin-producing dinoflagellates in the environment

Geology and genesis of Dounan manganese deposits, Yunnan Province, P. R. China / Baohong Hou.

Bibliography: leaves 280-288.xix, 288, [36] leaves, [15] leaves of plates : ill. (some col.), maps ; 30 cm.This study examines the medium sized sedimentary manganese deposit of Dounan, Yunnan Province of China, to determine the sedimentary environments controlling the distribution of ores and rocks, and to establish the relationships between ore mineralization and changes in the sedimentary environment. The thesis also aims to work out the sequence of events after the primary ore is formed, to determine which processes lead to secondary enrichment of the ore.Thesis (Ph.D.)--University of Adelaide, Dept. of Geology and Geophysics, 199

Effect of ultrasonic pre-treatment on coal slime flotation

Combined with the characteristics of flotation feed originating from China’s Panyidong Coal Preparation Plant, the ash, zeta potential, X-ray fluorescence spectroscopy and contact angle test were used to study changes in the surface properties of flotation feed under ultrasonic pre-treatment, and its effect on flotation of coal slime. Results show that Preferred pre-treatment process is ultrasonic secondary treatment, ultrasonic secondary pre-treatment can remove most of the high-ash fine mud for instance kaolinite, montmorillonite and quartz in the coal slurry, reduce the surface electronegativity of coal particles, and increase the contact angle of coal particles. Thus, the concentrate ash content decreases to 13%, the recovery rate, yield of flotation concentrate and combustible matter recovery reach 92.6%, 90.9% and 97.6%, respectively

Source of zircon in world-class heavy mineral placer deposits of the Cenozoic Eucla Basin, Southern Australia from LA-ICPMS U-Pb geochronology

The Eucla Basin of southern Australia is a newly recognised zircon-rich mineral sands province with mining operations underway at the world-class Jacinth-Ambrosia deposits. Detrital zircon U-Pb dating via laser ablation inductively coupled plasma mass spectrometry from samples distributed along the length of the Eucla Basin paleoshore system reveals the majority of zircons (c. 55%) are from c. 1300 to 1000. Ma source rocks. Many of the zircons of this age range have metamorphic textures indicating the source province(s) of these zircons underwent high-grade metamorphism during the Mesoproterozoic. A secondary provenance signature occurs at c. 1800-1600. Ma, with significant amounts of c. 1680-1600. Ma zircon. These two key age intervals, c. 1300-1000. Ma and c. 1800-1600. Ma match the major rock-forming intervals of the Albany Fraser Orogen and Musgrave Province, crystalline basement regions that crop out in the western and northern hinterland of the Eucla Basin and which are transected by extensive Early Cenozoic paleodrainage systems. The subordinant volume of Archean zircons in the paleoshoreline deposits are predominantly c. 2660. Ma or older and are most likely derived from the Yilgarn Craton. The primary source regions for the zircons thus lie to the west and north of the main sites of heavy mineral sand accumulation, located in the central and eastern portions of the paleoshoreline complex of the Eucla Basin. This is indicative of the dominant process of westerly longshore drift as the primary control on sediment movement and redistribution along much of the Eucla Basin coastline. Zircons of these ages were also likely derived from recycling sediments of Neoproterozoic and Phanerozoic intracontinental basins, in particular the Officer Basin, which contains dominantly c. 1350-1000. Ma zircons, and was widely incised by the Paleogene drainage network. Monazite U-Pb data from the Jacinth Mine records an abundance of c. 1350-1160. Ma grains, supporting source areas to the north and west of the Eucla Basin. Heavy mineral input from the more proximal Gawler Craton was minor. The zircon-rich mineral sands province of the Eucla Basin is thus a result of large-scale zircon erosion, transport, recycling and eventual concentration on beach shorelines where sand movement was controlled by dominant westerly longshore drift.19 page(s

Application of PAT-Based Feedback Control Approaches in Pharmaceutical Crystallization

Crystallization is one of the important unit operations for the separation and purification of solid products in the chemical, pharmaceutical, and pesticide industries, especially for realizing high-end, high-value solid products. The precise control of the solution crystallization process determines the polymorph, crystal shape, size, and size distribution of the crystal product, which is of great significance to improve product quality and production efficiency. In order to develop the crystallization process in a scientific method that is based on process parameters and data, process analysis technology (PAT) has become an important enabling platform. In this paper, we review the development of PAT in the field of crystallization in recent years. Based on the current research status of drug crystallization process control, the monitoring methods and control strategies of feedback control in the crystallization process were systematically summarized. The focus is on the application of model-free feedback control strategies based on the solution and solid information collected by various online monitoring equipment in product engineering, including improving particle size distribution, achieving polymorphic control, and improving purity. In this paper, the challenges of feedback control strategy in the crystallization process are also discussed, and the development trend of the feedback control strategy has been prospected

Study on Thermodynamics and Kinetics of Cephalexin Enzymatic Hydrolysis and Its Process Development to Prepare 7-ADCA

Cephalosporin enzymatic hydrolysis technology is a green technology for recovering 7-amino-3-deacetoxycephalosporanic acid (7-ADCA) from cephalosporin mother liquor. Solubility is critical for the production and purification of 7-ADCA. In this paper, the solubility of 7-ADCA and phenylglycine was measured. Solubility-temperature correlation model and solubility-pH correlation model were investigated, and Akaike information criterion (AIC) analysis was performed. The kinetic parameters of the enzymatic hydrolysis reaction of cephalexin, cefradine, and cefadroxil were determined, and the reaction rates under different substrate concentrations were measured, and the Lineweaver–Burk double-reciprocal equation was used to draw a graph. The Michaelis constants Km/(mg/mL) were 73.98, 583.84, 38.66, Vmax/(mg/mL·min) 4.20, 16.00, 1.96, respectively. The experimental results show that amphoteric compounds and buffers can prompt the reaction, low concentration of methanol promotes the reaction, while high concentration of methanol inhibits the reaction, and ethanol, isopropanol, tetrahydrofuran (THF), dimethyl sulfoxide (DMSO), ethylene glycol (EG), 1,4-dioxane all have different degrees of inhibition on the reaction speed. Finally, based on thermodynamic and kinetic studies, a process technology for the preparation of 7-ADCA by hydrolysis catalyzed of cephalexin was developed. It was confirmed that the proposed process route of preferential removal of phenylglycine by elution and/or cooling crystallization was reasonable and effective. The 7-ADCA crystal products obtained by crystallization were characterized by PXRD, thermal analysis, infrared, electron microscope, and high-performance liquid chromatography (HPLC)

Mechanisms and Characterization of Trichoderma longibrachiatum T6 in Suppressing Nematodes (Heterodera avenae) in Wheat

Heterodera avenae is an important soil-borne pathogen that affects field crops worldwide. Chemical nematicides can be used to control the nematode, but they bring toxicity to the environment and human. Trichoderma longibrachiatum has been shown to have the ability to control H. avenae cysts, but detailed microscopic observations and bioassays are lacking. In this study, we used microscopic observations and bioassays to study the effect of T. longibrachiatum T6 (TL6) on the eggs and second stage juveniles (J2s) of H. avenae, and investigate the role of TL6 in inducing the resistance to H. avenae in wheat seedling at physiological and biochemical levels. Microscopic observations recorded that TL6 parasitized on the H. avenae eggs, germinated, and produced a large number of hyphae on the eggs surface at the initial stage, thereafter, the eggs were completely surrounded by dense mycelia and the contents of eggs were lysed at the late stage. Meanwhile, the conidia suspension of TL6 parasitized on the surface of J2s, produced a large number of hyphae that penetrated the cuticle and caused deformation of the nematodes. TL6 at the concentration of 1.5 × 107 conidia ml−1 had the highest rates of parasitism on eggs and J2s, reflected by the highest hatching-inhibition of eggs and the mortality of J2s. In the greenhouse experiments, wheat seedlings treated with TL6 at 1.5 × 107 conidia ml−1 had reduced H. avenae infection, and increased plant growth significantly compared to the control. The cysts and juveniles in soil were reduced by 89.8 and 92.7%, the juveniles and females in roots were reduced by 88.3 and 91.3%, whereas the activity of chitinase and β-1, 3-glucanase, total flavonoids and lignin contents in wheat roots were increased significantly at different stage after inoculation with the eggs and TL6 conidia in comparison to the control. Maximum activity of chitinase and β-1, 3-glucanase were recorded at the 20th and 15th Days after inoculation with TL6 and thereafter it declined. The maximum contents of total flavonoids and lignin were recorded at the 35th and 40th Days after inoculation with TL6. After being stained with the rapid vital dyes of acridine orange (AO) and neutral red (NR), the frozen and infected eggs and J2s of H. avenae changed color to orange and red, respectively, while the color of eggs and J2s in control group did not change. Therefore, our results suggest that TL6 is potentially an effective bio-control agent for H. avenae. The possible mechanisms by which TL6 suppresses H. avenae infection are due to the direct parasitic and lethal effect of TL6 on the eggs and J2s activity, and the induced defense response in wheat plants together

Formation and Transformation Behavior of Sodium Dehydroacetate Hydrates

The effect of various controlling factors on the polymorphic outcome of sodium dehydroacetate crystallization was investigated in this study. Cooling crystallization experiments of sodium dehydroacetate in water were conducted at different concentrations. The results revealed that the rate of supersaturation generation played a key role in the formation of the hydrates. At a high supersaturation generation rate, a new sodium dehydroacetate dihydrate needle form was obtained; on the contrary, a sodium dehydroacetate plate monohydrate was formed at a low supersaturation generation rate. Furthermore, the characterization and transformation behavior of these two hydrated forms were investigated with the combined use of microscopy, powder X-ray diffraction (PXRD), Raman spectroscopy, Fourier transform infrared (FTIR), thermal gravimetric analysis (TGA), scanning electron microscopy (SEM) and dynamic vapor sorption (DVS). It was found that the new needle crystals were dihydrated and hollow, and they eventually transformed into sodium dehydroacetate monohydrate. In addition, the mechanism of formation of sodium dehydroacetate hydrates was discussed, and a process growth model of hollow crystals in cooling crystallization was proposed