Cyclic Bis(3'-5')diadenylic Acid (c-di-AMP) Analogs Promote the Activities of Photosynthesis and Respiration of <i>Chlamydomonas reinhardtii</i>

Physiological changes in the photosynthesis, respiration and cell division of Chlamydomonas reinhardtii, a freshwater green alga, in response to adenine nucleotides were investigated. In advance of this investigation, two adenine nucleotides, di(2'-O-methyl)-cyclic bis(3'-5')diadenylic acid (1) and its N-benzoyl-protected analog 2 were synthesized from the commercially available adenosine phosphoramidite. The respective analogs significantly promoted the cell division (cell number) of C. reinhardtii strains 137c mt+ and BR mt+. Moreover, they significantly enhanced the O2 evolution (photosynthesis) and O2 uptake (respiration) of both strains. c-di-AMP analogs seem to play an effective role as a physiological activator in planta.

Complexity Reduced MIMO Interleaved SC-FDMA Receiver with Iterative Detection

In this paper, we propose the receiver structure for Multiple Input Multiple Output (MIMO) Interleaved Single Carrier-Frequency Division Multiple Access (SC-FDMA) where the Frequency Domain Equalization (FDE) is firstly done for obtaining the tentative decision results and secondly using them the Inter-Symbol Interference (ISI) is cancelled by ISI canceller and then the Maximum Likelihood Detection (MLD) is used for separating the spatially multiplexed signals. Furthermore the output from MLD is fed back to ISI canceller repeatedly. In order to reduce the complexity, we replace the MLD by QR Decomposition with M-Algorithm (QRD-M) or Sphere Decoding (SD). Moreover, we add the soft output function to SD using Repeated Tree Search (RTS) algorithm to generate soft replica for ISI cancellation. We also refer to the Single Tree Search (STS) algorithm to further reduce the complexity of RTS. By examining the BER characteristics and the complexity reduction through computer simulations, we have verified the effectiveness of proposed receiver structure.

Molecules with a TEMPO-based head group as high-performance organic friction modifiers

High-performance organic friction modifiers(OFMs)added to lubricating oils are crucial for reducing energy loss and carbon footprint.To establish a new class of OFMs,we measured the friction and wear properties of N-(2,2,6,6-tetramethyl-1-oxyl-4-piperidinyl)dodecaneamide referred to as C12Amide-TEMPO.The effect of its head group chemistry,which is characterized by a rigid six-membered ring sandwiched by an amide group and a terminal free oxygen radical,was also investigated with both experiments and quantum mechanical(QM)calculations.The measurement results show that C12Amide-TEMPO outperforms the conventional OFMs of glyceryl monooleate(GMO)and stearic acid,particularly for load-carrying capacity,wear reduction,and stability of friction over time.The friction and wear reduction effect of C12Amide-TEMPO is also greatly superior to those of C12Ester-TEMPO and C12Amino-TEMPO,in which ester and amino groups replace the amide group,highlighting the critical role of the amide group.The QM calculation results suggest that,in contrast to C12Ester-TEMPO,C12Amino-TEMPO,and the conventional OFMs of GMO and stearic acid,C12Amide-TEMPO can form effective boundary films on iron oxide surfaces with a unique double-layer structure:a strong surface adsorption layer owing to the chemical interactions of the amide oxygen and free radical with iron oxide surfaces,and an upper layer owing to the interlayer hydrogen-bonding between the amide hydrogen and free radical or between the amide hydrogen and oxygen.Moreover,the intralayer hydrogen-bonding in each of the two layers is also possible.We suggest that in addition to strong surface adsorption,the interlayer and intralayer hydrogen-bonding also increases the strength of the boundary films by enhancing the cohesion strength,thereby resulting in the high tribological performance of C12Amide-TEMPO.The findings in this study are expected to provide new hints for the optimal molecular design of OFMs.