Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Recently, the synthesis of nanozymes-enzyme microsystems with high catalytic stability provides new opportunities for treating diverse pollutants in complex aquatic systems. Herein, a carboxyl-functionalized CuMn bimetallic nanozyme-enzyme microsystem (CMAC@Lipase) was successfully constructed by combining copper‑manganese based aminoclays (CMAC) with lipase. This system exhibited laccase-like catalytic activity facilitated by CuMn electron transfer, while enhancing lipase stability via its carrier function. Under alkaline conditions at pH 10, CMAC@Lipase catalyzed the hydrolysis of p-NPP (280 nm) to produce p-NP (400 nm), and subsequently reduced p-NP to p-AP within 30 min with the assistance of NaBH. Furthermore, it effectively degraded 72.8 % of dimethyl phthalate (DMP) at 40 mg·L under alkaline conditions within 48 h, maintaining a 53.5 % degradation rate after 10 reuse cycles. This work provided a new strategy for the design of nanozyme-enzyme microsystems and a new research idea for the efficient treatment of contaminants in actual aqueous environments.
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http://dx.doi.org/10.1016/j.ijbiomac.2024.138145 | DOI Listing |