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1.
Anal Biochem ; 694: 115618, 2024 Jul 14.
Artículo en Inglés | MEDLINE | ID: mdl-39009105

RESUMEN

OBJECTIVE: The objective of this research is to develop two methodologies, Enzymatic recombinase amplification (ERA) and Polymerase Chain Reaction (PCR) coupled with Lateral Flow Dipstick (LFD), for the swift authentication of Gastrodia elata. METHODOLOGY: Primers and nfo probes for the ERA of Gastrodia elata were developed based on the ITS2 genome sequences of Gastrodia elata and its counterfeits. Specific primers for the PCR analysis of Gastrodia elata were generated using the NCBI (National Center for Biotechnology Information) online platform. Through experimental validation, the optimal reaction system and conditions for both methodologies were established, and their efficacy was assessed. RESULTS: The methodologies developed herein are applicable for the targeted analysis of the medicinal species, Gastrodia elata. The sensitivity of the ERA-LFD detection method matched that of the conventional PCR-LFD approach, recorded at 1 ng µL-1. Consistency was observed in the results across three replicates of visualization test strips for both techniques. Upon evaluation, both the PCR-LFD and ERA-LFD methods demonstrated a total compliance rate of 100 %. CONCLUSION: The ERA-LFD and PCR-LFD methods facilitate reduced detection times and offer visual results. These techniques are particularly effective for on-site detection and quality control in the authentication of Gastrodia elata within traditional Chinese medicine markets and at the primary level of healthcare provision.

2.
Artículo en Inglés | MEDLINE | ID: mdl-31284528

RESUMEN

When cities develop rapidly, there are negative effects such as population expansion, traffic congestion, resource shortages, and pollution. It has become essential to explore new types of urban development patterns, and thus, the concept of the "smart city" has emerged. The purpose of this paper is to investigate the links between smart city policies and urban green total factor productivity (GTFP) in the context of China. Based on panel data of 200 cities in China from 2007-2016 and treating smart city policy as a quasi-natural experiment, the paper uses a difference-in-differences propensity score matching (PSM-DID) approach to prevent selection bias. The results show: (a) Smart city policies can significantly increase urban GTFP by 16% to 18%; (b) the larger the city, the stronger and more significant this promotion.


Asunto(s)
Política Ambiental/legislación & jurisprudencia , Regulación Gubernamental , Urbanización , China , Ciudades , Desarrollo Económico/estadística & datos numéricos , Modelos Económicos , Puntaje de Propensión
3.
Plant Mol Biol ; 68(1-2): 43-59, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18548197

RESUMEN

To begin biochemical and molecular studies on the biosynthesis of the type II arabinogalactan chains on arabinogalactan-proteins (AGPs), we adopted a bioinformatic approach to identify and systematically characterise the putative galactosyltransferases (GalTs) responsible for synthesizing the beta-(1,3)-Gal linkage from CAZy GT-family-31 from Arabidopsis thaliana. These analyses confirmed that 20 members of the GT-31 family contained domains/motifs typical of biochemically characterised beta-(1,3)-GTs from mammalian systems. Microarray data confirm that members of this family are expressed throughout all tissues making them likely candidates for the assembly of the ubiquitously found AGPs. One member, At1g77810, was selected for further analysis including location studies that confirmed its presence in the Golgi and preliminary enzyme substrate specificity studies that demonstrated beta-(1,3)-GalT activity. This bioinformatic/molecular study of CAZy GT-family-31 was validated by the recent report of Strasser et al. (Plant Cell 19:2278-2292, 2007) that another member of this family (At1g26810; GALT1) encodes a beta-(1,3)-GalT involved in the biosynthesis of the Lewis a epitope of N-glycans in Arabidopsis thaliana.


Asunto(s)
Proteínas de Arabidopsis/metabolismo , Arabidopsis/enzimología , Galactosiltransferasas/metabolismo , Secuencia de Aminoácidos , Animales , Arabidopsis/genética , Proteínas de Arabidopsis/clasificación , Proteínas de Arabidopsis/genética , Células COS , Chlorocebus aethiops , Técnica del Anticuerpo Fluorescente , Galactosiltransferasas/clasificación , Galactosiltransferasas/genética , Aparato de Golgi/metabolismo , Immunoblotting , Datos de Secuencia Molecular , Mucoproteínas/clasificación , Mucoproteínas/genética , Mucoproteínas/metabolismo , Análisis de Secuencia por Matrices de Oligonucleótidos , Filogenia , Proteínas de Plantas/clasificación , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Homología de Secuencia de Aminoácido , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción , Especificidad por Sustrato
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