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As a non-contact method, vision-based measurement for vibration extraction and modal parameter identification has attracted much attention. In most cases, artificial textures are crucial elements for visual tracking, and this feature limits the application of vision-based vibration measurement on textureless targets. As a computation technique for visualizing subtle variations in videos, the video magnification technique can analyze modal responses and visualize modal shapes, but the efficiency is low, and the processing results contain clipping artifacts. This paper proposes a novel method for the application of a modal test. In contrast to the deviation magnification that exaggerates subtle geometric deviations from only a single image, the proposed method extracts vibration signals with sub-pixel accuracy on edge positions by changing the perspective of deviations from space to timeline. Then, modal shapes are visualized by decoupling all spatial vibrations following the vibration theory of continuous linear systems. Without relying on artificial textures and motion magnification, the proposed method achieves high operating efficiency and avoids clipping artifacts. Finally, the effectiveness and practical value of the proposed method are validated by two laboratory experiments on a cantilever beam and an arch dam model.
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The phase-based motion magnification technique can exaggerate specific structural vibrations and obtain potential applications in visualizing and understanding modal shapes. However, the quality of motion magnification is affected by noise and clipping artifacts, especially in large amplifications. We propose a hybrid-driven motion magnification framework that combines Eulerian and Lagrangian motion processing. Since the structural global spatial vibration corresponding to different modal shapes usually accumulates energy differences in the timeline, from a Eulerian perspective, temporal intensity variations are denoised and separated according to the energy distribution to control spatial motions. Meanwhile, from a Lagrangian perspective, the motion magnification is realized by compensating spatial motion according to the magnified inter-frame motion vector field. By utilizing both Eulerian and Lagrangian motion processing, the proposed framework supports a larger amplification factor and achieves better performance in perceiving subtle vibrations in controlled modal tests.
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As a promising alternative to conventional contact sensors, vision-based technologies for a structural dynamic response measurement and health monitoring have attracted much attention from the research community. Among these technologies, Eulerian video magnification has a unique capability of analyzing modal responses and visualizing modal shapes. To reduce the noise interference and improve the quality and stability of the modal shape visualization, this study proposes a hybrid motion magnification framework that combines linear and phase-based motion processing. Based on the assumption that temporal variations can represent spatial motions, the linear motion processing extracts and manipulates the temporal intensity variations related to modal responses through matrix decomposition and underdetermined blind source separation (BSS) techniques. Meanwhile, the theory of Fourier transform profilometry (FTP) is utilized to reduce spatial high-frequency noise. As all spatial motions in a video are linearly controllable, the subsequent phase-based motion processing highlights the motions and visualizes the modal shapes with a higher quality. The proposed method is validated by two laboratory experiments and a field test on a large-scale truss bridge. The quantitative evaluation results with high-speed cameras demonstrate that the hybrid method performs better than the single-step phase-based motion magnification method in visualizing sound-induced subtle motions. In the field test, the vibration characteristics of the truss bridge when a train is driving across the bridge are studied with a commercial camera over 400 m away from the bridge. Moreover, four full-field modal shapes of the bridge are successfully observed.
Assuntos
Som , Vibração , Movimento (Física) , Análise de FourierRESUMO
Anisomycin (compound 1), a pyrrolidine antibiotic, exhibits diverse biological and pharmacologic activities. The biosynthetic gene cluster of compound 1 has been identified previously, and the multistep assembly of the core benzylpyrrolidine scaffold was characterized. However, enzymatic modifications, such as acylation, involved in compound 1 biosynthesis are unknown. In this study, the genetic manipulation of aniI proved that it encoded an indispensable acetyltransferase for compound 1 biosynthesis. Bioinformatics analysis suggested AniI as a member of maltose (MAT) and galactoside O-acetyltransferases (GAT) with C-terminal left-handed parallel beta-helix (LbH) subdomain, which were referred to as LbH-MAT-GAT sugar O-acetyltransferases. However, the biochemical assay identified that its target site was the hydroxyl group of the pyrrolidine ring. AniI was found to be tolerant of acyl donors with different chain lengths for the biosynthesis of compound 1 and derivatives 12 and 13 with butyryl and isovaleryl groups, respectively. Meanwhile, it showed comparable activity toward biosynthetic intermediates and synthesized analogues, suggesting promiscuity to the pyrrolidine ring structure of compound 1. These data may inspire new viable synthetic routes for the construction of more complex pyrrolidine ring scaffolds in compound 1. Finally, the overexpression of aniI under the control of strong promoters contributed to the higher productivities of compound 1 and its analogues. These findings reported here not only improve the understanding of anisomycin biosynthesis but also expand the substrate scope of O-acetyltransferase working on the pyrrolidine ring and pave the way for future metabolic engineering construction of high-yield strains. IMPORTANCE Acylation is an important tailoring reaction during natural product biosynthesis. Acylation could increase the structural diversity and affect the chemical stability, volatility, biological activity, and even the cellular localization of specialized compounds. Many acetyltransferases have been reported in natural product biosynthesis. The typical example of the LbH-MAT-GAT sugar O-acetyltransferase subfamily was reported to catalyze the coenzyme A (CoA)-dependent acetylation of the 6-hydroxyl group of sugars. However, no protein of this family has been characterized to acetylate a nonsugar secondary metabolic product. Here, AniI was found to catalyze the acylation of the hydroxyl group of the pyrrolidine ring and be tolerant of diverse acyl donors and acceptors, which made the biosynthesis more efficient and exclusive for biosynthesis of compound 1 and its derivatives. Moreover, the overexpression of aniI serves as a successful example of genetic manipulation of a modification gene for the high production of final products and might set the stage for future metabolic engineering.
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Acetiltransferases/metabolismo , Anisomicina/biossíntese , Antibacterianos/biossíntese , Acetilcoenzima A/metabolismo , Acetiltransferases/genética , Acilação , Escherichia coli/genéticaRESUMO
A new medermycin analog (1) was isolated from the marine-derived actinomycetes Streptomyces sp. ZS-A45. The structure elucidation of compound 1 was determined by the HRESIMS and extensive NMR analysis. And compound 1 exhibited significant cytotoxicity against PC3 cell lines with IC50 values of 0.81 ± 0.42 µm.
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Actinobacteria/metabolismo , Antibacterianos/isolamento & purificação , Antibacterianos/química , Antibacterianos/farmacologia , Linhagem Celular Tumoral , Dicroísmo Circular , Humanos , Espectroscopia de Ressonância Magnética , Biologia Marinha , Naftoquinonas/isolamento & purificaçãoRESUMO
Four new medermycin-type naphthoquinones, strepoxepinmycins A-D (1-4), and one known compound, medermycin (5), were identified from Streptomyces sp. XMA39. Their structures were elucidated by analysis of HRESIMS, 1D and 2D NMR spectroscopic data, and ECD calculations. Among these compounds, strepoxepinmycin A (1) represents a rare 5,10-oxepindione ring system typically formed by a Baeyer-Villiger oxidation, and strepoxepinmycin B (2) is an isolation artifact derived from 1. Bioactivity evaluations of these compounds showed that compounds 3 and 4 exhibited cytotoxicity against HCT-116 and PC-3 cancer cell lines and 4 exhibited moderate inhibition of ROCK 2 protein kinase. In addition, all of the new compounds showed antibacterial activity against Escherichia coli and methicillin-resistant Staphylococcus aureus and antifungal activity against Candida albicans.
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Naftoquinonas/isolamento & purificação , Streptomyces/metabolismo , Microbiologia da Água , Anti-Infecciosos/farmacologia , Antineoplásicos/farmacologia , Linhagem Celular Tumoral , Humanos , Naftoquinonas/química , Naftoquinonas/farmacologiaRESUMO
Bromodomains (BRD) are readers of the epigenetic code that regulate gene transcription through their recognition of acetyl-lysine modified histone tails. Recently, bromodomain-containing proteins such as BRD4 have been demonstrated to be druggable through the discovery of potent inhibitors. These protein-protein interaction inhibitors have the potential to modulate multiple diseases by their profound anti-inflammatory and antiproliferative effects. In order to explore new BRD4 inhibitors as well as lead compounds for the development of new drugs, the secondary metabolites of Alternaria sp. NH-F6, a fungus isolated from deep-sea sediment samples, were analyzed systematically. Five new compounds including two new perylenequinones (1-2), one new alternaric acid (3), 2-(N-vinylacetamide)-4-hydroxymethyl-3-ene-butyrolactone (4), one new cerebroside (5), together with 19 known compounds (6-24) were isolated from the ethyl acetate extracts of this strain. Their structures were elucidated using nuclear magnetic resonance (NMR) and high resolution electrospray ionization mass spectrometry (HR-ESI-MS) analyses. Finally, all these compounds were evaluated for their inhibitory activity against BRD4 protein, and compound 2 exhibited a potent inhibition rate of 88.1% at a concentration of 10 µM. This research provides a new BRD4 inhibitor which may possess potential antitumoral, antiviral, or anti-inflammatory pharmaceutical values.
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Alternaria/química , Organismos Aquáticos/química , Fatores Biológicos/química , Fatores Biológicos/farmacologia , Fungos/química , Fatores de Transcrição/antagonistas & inibidores , Espectroscopia de Ressonância Magnética/métodos , Espectrometria de Massas por Ionização por Electrospray/métodosRESUMO
On the basis of the one strain-many compounds strategy, five compounds including two new holomycin derivatives 2 - 3, two new cyclopropaneacetic acid derivatives 4 - 5, together with one known compound holomycin (1) were isolated from a marine-derived bacterium Streptomyces sp. DT-A37. Their structures were elucidated using NMR and HR-ESI-MS analyses. All these compounds were evaluated for their antimicrobial activity, cytotoxic activity, and inhibitory activity against BRD4 protein. Compound 1 exhibited potent cytotoxicity against H1975 cells with IC50 value of 1 µm, and its minimal inhibitory concentration values against Escherichia coli and Staphylococcus aureus were both 64 µm.
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Ciclopropanos/química , Ciclopropanos/farmacologia , Lactamas/química , Lactamas/farmacologia , Streptomyces/química , Anti-Infecciosos/química , Anti-Infecciosos/farmacologia , Bactérias/efeitos dos fármacos , Infecções Bacterianas/tratamento farmacológico , Candida/efeitos dos fármacos , Candidíase/tratamento farmacológico , Proteínas de Ciclo Celular , Linhagem Celular , Humanos , Espectroscopia de Ressonância Magnética , Proteínas Nucleares/antagonistas & inibidores , Espectrometria de Massas por Ionização por Electrospray , Fatores de Transcrição/antagonistas & inibidoresRESUMO
Rotational angle and speed are important parameters for condition monitoring and fault diagnosis of rotating machineries, and their measurement is useful in precision machining and early warning of faults. In this study, a novel vision-based measurement algorithm is proposed to complete this task. A high-speed camera is first used to capture the video of the rotational object. To extract the rotational angle, the template-based Lucas-Kanade algorithm is introduced to complete motion tracking by aligning the template image in the video sequence. Given the special case of nonplanar surface of the cylinder object, a nonlinear transformation is designed for modeling the rotation tracking. In spite of the unconventional and complex form, the transformation can realize angle extraction concisely with only one parameter. A simulation is then conducted to verify the tracking effect, and a practical tracking strategy is further proposed to track consecutively the video sequence. Based on the proposed algorithm, instantaneous rotational speed (IRS) can be measured accurately and efficiently. Finally, the effectiveness of the proposed algorithm is verified on a brushless direct current motor test rig through the comparison with results obtained by the microphone. Experimental results demonstrate that the proposed algorithm can extract accurately rotational angles and can measure IRS with the advantage of noncontact and effectiveness.
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The development of image sensor and optics enables the application of vision-based techniques to the non-contact dynamic vibration analysis of large-scale structures. As an emerging technology, a vision-based approach allows for remote measuring and does not bring any additional mass to the measuring object compared with traditional contact measurements. In this study, a high-speed vision-based sensor system is developed to extract structure vibration signals in real time. A fast motion extraction algorithm is required for this system because the maximum sampling frequency of the charge-coupled device (CCD) sensor can reach up to 1000 Hz. Two efficient subpixel level motion extraction algorithms, namely the modified Taylor approximation refinement algorithm and the localization refinement algorithm, are integrated into the proposed vision sensor. Quantitative analysis shows that both of the two modified algorithms are at least five times faster than conventional upsampled cross-correlation approaches and achieve satisfactory error performance. The practicability of the developed sensor is evaluated by an experiment in a laboratory environment and a field test. Experimental results indicate that the developed high-speed vision-based sensor system can extract accurate dynamic structure vibration signals by tracking either artificial targets or natural features.
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Two new cyclodipeptide (CDP) derivatives (1-2) and another seven known cyclodipeptides (3-9) were isolated from Streptomyces 26D9-414 by the genome mining approach combined with genetic dereplication and the "one strain many compounds" (OSMAC) strategy. The structures of the new CDPs were established on the basis of 1D- and 2D-NMR and comparative electronic circular dichroism (ECD) spectra analysis. The biosynthetic gene clusters (BGCs) for these CDPs were identified through antiSMASH analysis. The relevance between this cdp cluster and the identified nine CDPs was established by genetic interruption manipulation. The newly discovered natural compound 2 displayed comparable cytotoxicity against MDA-MB-231 and SW480 with that of cisplatin, a widely used chemotherapeutic agent for the treatment of various cancers.
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This note reports an efficient singular value decomposition (SVD)-based vibration extraction approach that recovers sound information in silent high-speed video. A high-speed camera of which frame rates are in the range of 2 kHz-10 kHz is applied to film the vibrating objects. Sub-images cut from video frames are transformed into column vectors and then reconstructed to a new matrix. The SVD of the new matrix produces orthonormal image bases (OIBs) and image projections onto specific OIB can be recovered as understandable acoustical signals. Standard frequencies of 256 Hz and 512 Hz tuning forks are extracted offline from their vibrating surfaces and a 3.35 s speech signal is recovered online from a piece of paper that is stimulated by sound waves within 1 min.