<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(4)</volume><submitter>Kaman WE</submitter><pubmed_abstract>Previously we described the discovery of a Bacillus spp. specific peptidase activity related to d-stereospecific peptidases (DSPs). The peptidase showed a strong preference for d-leucine and d-valine amino acids. These amino acids are present in the structure of the non-ribosomal peptide (NRP) antibiotics gramicidin A, B and C and polymyxin E. To examine if the Bacillus spp. DSP-related peptidase can hydrolyze these NRPs, the effect of gramicidin A and C and polymyxin E on peptidase activity in Bacillus anthracis culture supernatant was monitored. It was found that both gramicidins inhibited the DSP-related activity in a competitive manner. MALDI-TOF analysis revealed that upon incubation with B. anthracis culture supernatant gramicidin A hydrolyzation products appeared. This study shows that the Bacillus spp. specific DSP-like peptidase was potentially produced by the bacteria to gain intrinsic resistance against NRP antibiotics. These results are of utmost importance in research towards antimicrobial resistance, whereas transfer of DSP-related activity to other clinically relevant pathogens can be a serious threat to human health.</pubmed_abstract><journal>Environmental microbiology reports</journal><pagination>570-576</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9541196</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Gramicidin A is hydrolyzed by a d-stereospecific peptidase produced by Bacillus anthracis.</pubmed_title><pmcid>PMC9541196</pmcid><pubmed_authors>Kaman WE</pubmed_authors><pubmed_authors>Bikker FJ</pubmed_authors><pubmed_authors>Voskamp-Visser AI</pubmed_authors><pubmed_authors>Nazmi K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gramicidin A is hydrolyzed by a d-stereospecific peptidase produced by Bacillus anthracis.</name><description>Previously we described the discovery of a Bacillus spp. specific peptidase activity related to d-stereospecific peptidases (DSPs). The peptidase showed a strong preference for d-leucine and d-valine amino acids. These amino acids are present in the structure of the non-ribosomal peptide (NRP) antibiotics gramicidin A, B and C and polymyxin E. To examine if the Bacillus spp. DSP-related peptidase can hydrolyze these NRPs, the effect of gramicidin A and C and polymyxin E on peptidase activity in Bacillus anthracis culture supernatant was monitored. It was found that both gramicidins inhibited the DSP-related activity in a competitive manner. MALDI-TOF analysis revealed that upon incubation with B. anthracis culture supernatant gramicidin A hydrolyzation products appeared. This study shows that the Bacillus spp. specific DSP-like peptidase was potentially produced by the bacteria to gain intrinsic resistance against NRP antibiotics. These results are of utmost importance in research towards antimicrobial resistance, whereas transfer of DSP-related activity to other clinically relevant pathogens can be a serious threat to human health.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-04-08T13:41:21.372Z</modification><creation>2025-04-19T04:47:56.833Z</creation></dates><accession>S-EPMC9541196</accession><cross_references><pubmed>35403341</pubmed><doi>10.1111/1758-2229.13069</doi></cross_references></HashMap>