{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T09:25:51Z","timestamp":1790673951233,"version":"4.1.0"},"reference-count":34,"publisher":"National Academy of Sciences","issue":"16","content-domain":{"domain":["www.pnas.org"],"crossmark-restriction":true},"short-container-title":["Proc. Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[1998,8,4]]},"abstract":"<jats:p>\n                    The principal cause of bacterial resistance to penicillin and other \u03b2-lactam antibiotics is the acquisition of plasmid-encoded \u03b2-lactamases, enzymes that catalyze hydrolysis of the \u03b2-lactam bond and render these antibiotics inactive. Clavulanic acid is a potent inhibitor of \u03b2-lactamases and has proven clinically effective in combating resistant infections. Although clavulanic acid and penicillin share marked structural similarities, the biosyntheses of their bicyclic nuclei are wholly dissimilar. In contrast to the efficient iron-mediated oxidative cyclization of a tripeptide to isopenicillin N, the critical \u03b2-lactam ring of clavulanic acid is demonstrated to form by intramolecular closure catalyzed by a new type of ATP\/Mg\n                    <jats:sup>2+<\/jats:sup>\n                    -dependent enzyme, a \u03b2-lactam synthetase (\u03b2-LS). Insertional inactivation of its encoding gene in wild-type\n                    <jats:italic>Streptomyces clavuligerus<\/jats:italic>\n                    resulted in complete loss of clavulanic acid production and the accumulation of N\n                    <jats:sup>2<\/jats:sup>\n                    -(carboxyethyl)-\n                    <jats:sc>l<\/jats:sc>\n                    -arginine (CEA). Chemical complementation of this blocked mutant with authentic deoxyguanidinoproclavaminic acid (DGPC), the expected product of the \u03b2-LS, restored clavulanic acid synthesis. Finally, overexpression of this gene gave the \u03b2-LS, which was shown to mediate the conversion of CEA to DGPC in the presence of ATP\/Mg\n                    <jats:sup>2+<\/jats:sup>\n                    . Primary amino acid sequence comparisons suggest that this mode of \u03b2-lactam formation could be more widely spread in nature and mechanistically related to asparagine synthesis.\n                  <\/jats:p>","DOI":"10.1073\/pnas.95.16.9082","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T10:39:15Z","timestamp":1027679955000},"page":"9082-9086","update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":98,"title":["\u03b2-Lactam synthetase: A new biosynthetic enzyme"],"prefix":"10.1073","volume":"95","author":[{"given":"Brian O.","family":"Bachmann","sequence":"first","affiliation":[{"name":"Department of Chemistry, The Johns Hopkins University, 3400 North Charles Street, Baltimore, MD 21218"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rongfeng","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Chemistry, The Johns Hopkins University, 3400 North Charles Street, Baltimore, MD 21218"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Craig A.","family":"Townsend","sequence":"additional","affiliation":[{"name":"Department of Chemistry, The Johns Hopkins University, 3400 North Charles Street, Baltimore, MD 21218"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"341","published-online":{"date-parts":[[1998,8,4]]},"reference":[{"key":"e_1_3_4_1_2","doi-asserted-by":"crossref","first-page":"724","DOI":"10.1126\/science.270.5237.724","volume":"270","author":"Service R F","year":"1995","unstructured":"R F Service Science 270, 724\u2013727 (1995).","journal-title":"Science"},{"key":"e_1_3_4_2_2","doi-asserted-by":"crossref","first-page":"1064","DOI":"10.1126\/science.257.5073.1064","volume":"257","author":"Neu H C","year":"1992","unstructured":"H C Neu Science 257, 1064\u20131073 (1992).","journal-title":"Science"},{"key":"e_1_3_4_3_2","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1039\/np9971400309","volume":"14","author":"Baggaley K H","year":"1997","unstructured":"K H Baggaley, A G Brown, C J Schofield Nat Prod Rep 14, 309\u2013333 (1997).","journal-title":"Nat Prod Rep"},{"key":"e_1_3_4_4_2","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1126\/science.279.5348.199","volume":"279","author":"Marsden A F A","year":"1998","unstructured":"A F A Marsden, B Wilkinson, J Cortes, N J Dunster, J Staunton, P F Leadlay Science 279, 199\u2013202 (1998).","journal-title":"Science"},{"key":"e_1_3_4_5_2","doi-asserted-by":"crossref","first-page":"367","DOI":"10.1126\/science.277.5324.367","volume":"277","author":"Jacobsen J R","year":"1997","unstructured":"J R Jacobsen, C R Hutchinson, D E Cane, C Khosla Science 277, 367\u2013369 (1997).","journal-title":"Science"},{"key":"e_1_3_4_6_2","doi-asserted-by":"crossref","first-page":"875","DOI":"10.1146\/annurev.mi.47.100193.004303","volume":"47","author":"Katz L","year":"1993","unstructured":"L Katz, S Donadio Annu Rev Microbiol 47, 875\u2013912 (1993).","journal-title":"Annu Rev Microbiol"},{"key":"e_1_3_4_7_2","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1146\/annurev.mi.49.100195.001221","volume":"49","author":"Hutchinson C R","year":"1995","unstructured":"C R Hutchinson, I Fujii Annu Rev Microbiol 49, 201\u2013238 (1995).","journal-title":"Annu Rev Microbiol"},{"key":"e_1_3_4_8_2","doi-asserted-by":"crossref","first-page":"2651","DOI":"10.1021\/cr960029e","volume":"97","author":"Marahiel M A","year":"1997","unstructured":"M A Marahiel, T Stachelhaus, H D Mootz Chem Rev 97, 2651\u20132673 (1997).","journal-title":"Chem Rev"},{"key":"e_1_3_4_9_2","doi-asserted-by":"crossref","first-page":"2675","DOI":"10.1021\/cr9600262","volume":"97","author":"von D\u00f6hren H","year":"1997","unstructured":"H von D\u00f6hren, U Keller, J Vater, R Zocher Chem Rev 97, 2675\u20132705 (1997).","journal-title":"Chem Rev"},{"key":"e_1_3_4_10_2","doi-asserted-by":"crossref","first-page":"827","DOI":"10.1038\/42990","volume":"387","author":"Roach P L","year":"1997","unstructured":"P L Roach, I J Clifton, C M H Hensgens, N Shibata, C J Schofield, J Hajdu, J E Baldwin Nature (London) 387, 827\u2013830 (1997).","journal-title":"Nature (London)"},{"key":"e_1_3_4_11_2","doi-asserted-by":"crossref","first-page":"721","DOI":"10.1016\/S1074-5521(97)90310-0","volume":"4","author":"Townsend C A","year":"1997","unstructured":"C A Townsend Chem Biol 4, 721\u2013730 (1997).","journal-title":"Chem Biol"},{"key":"e_1_3_4_12_2","doi-asserted-by":"crossref","unstructured":"Elson S. 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