[Microbial Diversity of Filamentous Sludge Bulking at Low Temperature].

To investigate the characteristics of microbial diversity during filamentous bulking at low temperature, the induction of sludge bulking was successfully carried out using a low-temperature sequencing batch reactor(SBR). With the help of Illumina MiSeq high-throughput sequencing technology, the overall changes in the microbial community structure of activated sludge, the characteristics of each specific microbial community, and the specific genera were all investigated under different sludge sedimentation performances. The results showed that filamentous bulking can be successfully induced after the system operating temperature drops to (14±1)℃, and the COD and TN removal rates can still be maintained at approximately 90% and 86%, respectively, with the sludge volume index deteriorating to 663.99 mL·g-1. The occurrence of sludge bulking at low temperature will not only reduce the overall diversity and uniformity of microorganisms in the system and increase the abundance of filamentous bacteria from 0.49% to 26.04% but also cause the abundance of denitrifying bacteria to reduce from 21.04% to 13.99% and that of dephosphorization bacteria to reduce from 4.25% to 1.93%. Of the five filamentous genera founded, the abundances of three filamentous bacteria represented by Thiothrix increased, whereas only that of the Haliscomenobacter decreased. Of the 19 denitrifier genera founded, the abundances of five species represented by Nitrosomonas increased, whereas those of seven species represented by Nitrospira decreased. Moreover, the abundances of Pseudomonas and Tetrasphaera increased out of the eight phosphorus-removing bacteria genera, whereas the abundances of the five bacteria genera represented by Candidatus_Competibacter decreased. Although sludge bulking has a significant impact on the structure of the microbial community, the 477 operational taxonomic units and 227 bacterial species that are always present in the different sludge samples indicate that the main microorganisms in the reactor are still relatively stable during the bulking process.

[Ultracytochemical localization of enzymes and DNA analysis during the development of garlic].

It is believed that during storage, the parenchyma cells of garlic (Allium sativum L.) bulb would wither and fade gradually, and nutrients released inside the cells become available for the germination and growth of the young bud. In this study, The distributions of acid phosphatase (APase) and Adenosine Triphosphatase (ATPase) during germination were analyzed based on the method of lead precipitation at the electron microscopic level. It was found that their activities presenting in plasma membrane, cell wall and plasmodesma increased along the different developmental periods during storage. The fact that the most intensive enzymatic activity of APase and ATPase appeared at germination indicates that degradation, transformation and exportation of cell matrix are helpful in complete translocation of nutrient to new bud. The DNA in the degrading parenchyma cells was analyzed using the agarose electrophoresis. Results clearly showed a typical DNA ladder on the gel, indicating that gene-controlled, programmed cell death may contribute to the degradation of garlic parenchyma cells.

[Studies on the change of intercellular connection and the appearance and function of ectodesmata-like structure in garlic clove during the dormancy development].

The characteristics of intercellular connection have been observed during the dormancy development of garlic by the transmission electron microscope (TEM). The results indicated that the appearances of the different states of intercellular connection were physiological adaptation to the development of garlic clove during storage. Ectodesmata-like existed at the wall boundary between the declining tissue and the living cells in the garlic during germination period. By Confocal Laser Scanning Microscopy (CLSM) combined with fluorescence probe, 457Da Lucifer Yellow (LYCH) which was impermeable to the membrane, could enter the living parenchyma cell through symplastic route. The result proved that ectodesmata-like structure, which may be recognized as the modified plasmodesata, still retained physiological activity during a certain time and function as the channels of the symplastic transport of nutrient.