An autonomous system of detecting and attracting leafhopper males using species- and sex-specific substrate borne vibrational signals

2016 ◽  
Vol 123 ◽  
pp. 29-39 ◽  
Author(s):  
G. Korinšek ◽  
M. Derlink ◽  
M. Virant-Doberlet ◽  
T. Tuma
Keyword(s):  
Autonomous System ◽  
Specific Substrate ◽  
Vibrational Signals

scholarly journals Effects of Sinusoidal Vibrations on the Motion Response of Honeybees

2021 ◽  
Vol 9 ◽  
Author(s):  
Martin Stefanec ◽  
Hannes Oberreiter ◽  
Matthias A. Becher ◽  
Gundolf Haase ◽  
Thomas Schmickl
Keyword(s):  
Specific Substrate ◽  
Simple Method ◽  
Amplitude Control ◽  
Bee Colony ◽  
Motion Activity ◽  
Vibrational Signals ◽  
Animal Interaction ◽  
Chaotic Nature ◽  
Communication Pathway ◽  
Vibratory Signals

Vibratory signals play a major role in the organization of honeybee colonies. Due to the seemingly chaotic nature of the mechano-acoustic landscape within the hive, it is difficult to understand the exact meaning of specific substrate-borne signals. Artificially generated vibrational substrate stimuli not only allow precise frequency and amplitude control for studying the effects of specific stimuli, but could also provide an interface for human-animal interaction for bee-keeping-relevant colony interventions. We present a simple method for analyzing motion activity of honeybees and show that specifically generated vibrational signals can be used to alter honeybee behavior. Certain frequency-amplitude combinations can induce a significant decrease and other signals might trigger an increase in honeybees’ motion activity. Our results demonstrate how different subtle local modulatory signals on the comb can influence individual bees in the local vicinity of the emitter. Our findings could fundamentally impact our general understanding of a major communication pathway in honeybee colonies. This pathway is based on mechanic signal emission and mechanic proprio-reception of honeybees in the bee colony. It is a candidate to be a technologically accessible gateway into the self-regulated system of the colony and thus may offer a novel information transmission interface between humans and honeybees for the next generation of “smart beehives” in future beekeeping.

The Demonstration of Human Prostatic Acid Phosphatase (Pap) With Phosphorylcholine

1976 ◽  
Vol 34 ◽  
pp. 88-89
Author(s):  
José A. Serrano ◽  
Hannah L. Wasserkrug ◽  
Anna A. Serrano ◽  
Arnold M. Seligman
Keyword(s):  
Acid Phosphatase ◽  
Prostate Gland ◽  
Prostatic Acid Phosphatase ◽  
Human Prostate ◽  
Rat Tissues ◽  
Specific Substrate ◽  
Acid Phosphatases ◽  
Lysosomal Acid ◽  
Cacodylate Buffer

As previously reported (1, 2) phosphorylcholine (PC) is a specific substrate for prostatatic acid phosphatase (PAP) as opposed to other acid phosphatases, e.g., lysosomal acid phosphatase. The specificity of PC for PAP is due to the pentavalent nitrogen in PC, a feature that renders PC resistant to hydrolysis by all other acid phosphatases. Detailed comparative cytochemical results in rat tissues are in press. This report deals with ultracytochemical results applying the method to normal and pathological human prostate gland.Fresh human prostate was obtained from 7 patients having transurethral resections or radical prostatectomies. The tissue was fixed in 3% glutaraldehyde- 0.1 M cacodylate buffer (pH 7.4) for 15 min, sectioned at 50 μm on a Sorvall TC-2 tissue sectioner, refixed for a total of 2 hr, and rinsed overnight in 0.1 M cacodylate buffer (pH 7.4)-7.5% sucrose.

Prostatic Acid Phosphatase (PAP) Differentiated Ultracytochemically from Lysosomal Acid Phosphate in the Rat with a PAP/Specific Substrate, Phosphorylcholine

1975 ◽  
Vol 33 ◽  
pp. 450-451
Author(s):  
W. Allen Shannon ◽  
José A. Serrano ◽  
Hannah L. Wasserkrug ◽  
Anna A. Serrano ◽  
Arnold M. Seligman
Keyword(s):  
Acid Phosphatase ◽  
Phosphate Buffer ◽  
Prostatic Carcinoma ◽  
Prostatic Acid Phosphatase ◽  
Chemotherapeutic Agents ◽  
Specific Substrate ◽  
Acid Phosphate ◽  
Lysosomal Acid ◽  
Design And Synthesis ◽  
New Chemotherapeutic Agents

During the design and synthesis of new chemotherapeutic agents for prostatic carcinoma based on phosphorylated agents which might be enzyme-activated to cytotoxicity, phosphorylcholine, [(CH3)3+NCH2CH2OPO3Ca]Cl-, has been indicated to be a very specific substrate for prostatic acid phosphatase (PAP). This phenomenon has led to the development of specific histochemical and ultracytochemical methods for PAP using modifications of the Gomori lead method for acid phosphatase. Comparative histochemical results in prostate and kidney of the rat have been published earlier with phosphorylcholine (PC) and β-glycerophosphate (βGP). We now report the ultracytochemical results.Minced tissues were fixed in 3% glutaraldehyde-0.1 M phosphate buffered (pH 7.4) for 1.5 hr and rinsed overnight in several changes of 0.05 M phosphate buffer (pH 7.0) containing 7.5% sucrose. Tissues were incubated 30 min to 2 hr in Gomori acid phosphatase medium (2) containing 0.1 M substrate, either PC or βGP.

AUTONOMOUS HEAT SUPPORT SYSTEM OF ELECTRONIC BLOCKS OF SPACE APPLIANCES

2018 ◽  
pp. 72-78
Author(s):  
A. V. Gorbunov ◽  
Yu. A. Zhukov ◽  
E. V. Korotkov ◽  
A. V. Lekanov ◽  
V. G. Porpylev ◽  
...  
Keyword(s):  
Thermal Regime ◽  
Autonomous System ◽  
Supply Voltage ◽  
Operating Temperature ◽  
Electronic Devices ◽  
Space Technology ◽  
Structural Scheme ◽  
Spacecraft Design ◽  
Temperature Controlled ◽  
Operating Temperature Range

The vast majority of electronic devices on-Board Russian spacecraft is placed on a temperature-controlled mounting surface is ON, however, in some tasks there is a necessity to place a separate electronic units out thermostated panels on remote spacecraft design. The article presents an autonomous system of providing thermal regime of electronic blocks of spacecraft and objects of space technology that require maintaining the operating temperature and are unable to be installed on the thermostatic landing surfaces of spacecraft. The proposed autonomous system of providing thermal regime can operate autonomously in the extended operating temperature range of the installation surface from -80 to +80 °C when the supply voltage changes in the range from 75 to 550% of the nominal value. The review of the existing solutions is presented, the substantiation of the proposed decision is given, the structural scheme of autonomous system of providing thermal regime is given and its description and an example of application is given.

scholarly journals Enhanced Production of the Mical Redox Domain for Enzymology and F-actin Disassembly Assays

2021 ◽  
Vol 22 (4) ◽  
pp. 1991
Author(s):  
Jimok Yoon ◽  
Heng Wu ◽  
Ruei-Jiun Hung ◽  
Jonathan R. Terman
Keyword(s):  
Nicotinamide Adenine Dinucleotide Phosphate ◽  
Actin Dynamics ◽  
Specific Substrate ◽  
Actin Assembly ◽  
Redox Enzymes ◽  
Enhanced Production ◽  
Reversible Redox ◽  
Future Work ◽  
Signaling Process

To change their behaviors, cells require actin proteins to assemble together into long polymers/filaments—and so a critical goal is to understand the factors that control this actin filament (F-actin) assembly and stability. We have identified a family of unusual actin regulators, the MICALs, which are flavoprotein monooxygenase/hydroxylase enzymes that associate with flavin adenine dinucleotide (FAD) and use the co-enzyme nicotinamide adenine dinucleotide phosphate (NADPH) in Redox reactions. F-actin is a specific substrate for these MICAL Redox enzymes, which oxidize specific amino acids within actin to destabilize actin filaments. Furthermore, this MICAL-catalyzed reaction is reversed by another family of Redox enzymes (SelR/MsrB enzymes)—thereby revealing a reversible Redox signaling process and biochemical mechanism regulating actin dynamics. Interestingly, in addition to the MICALs’ Redox enzymatic portion through which MICALs covalently modify and affect actin, MICALs have multiple other domains. Less is known about the roles of these other MICAL domains. Here we provide approaches for obtaining high levels of recombinant protein for the Redox only portion of Mical and demonstrate its catalytic and F-actin disassembly activity. These results provide a ground state for future work aimed at defining the role of the other domains of Mical — including characterizing their effects on Mical’s Redox enzymatic and F-actin disassembly activity.

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