Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Suspensions of were not affected by lysozyme alone, but in solutions of appropriate pH and ionic strength some lysozyme was bound to the bacterial surface and remained available for action if the bacteria were subsequently treated with antibody and complement. In the presence of antibody, complement had a relatively prolonged action on ending in lysis. However, from an early stage in the reaction this lysis could be accelerated by adding lysozyme. The results suggest that human complement acted on the outer, lipoprotein—lipopolysaccharide layers of the bacterial cell wall and so gave lysozyme access to the deeper mucopeptide. When the number of bound lysozyme molecules per bacterium was less than 10,000–20,000 the lysozyme effect decreased rapidly. However, many of these molecules may have been inactivated by K antigen.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1409634 | PMC |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!