Färber P, Geisen R
Federal Research Centre for Nutrition, Institute for Hygiene and Toxicology, Karlsruhe, Germany.
Appl Environ Microbiol. 1994 Sep;60(9):3401-4. doi: 10.1128/aem.60.9.3401-3404.1994.
Defined strains of the genus Penicillium used as starter cultures for food and strains isolated from mold-fermented foods were analyzed for their ability to inhibit the growth of Micrococcus luteus DSM 348 used as an indicator organism. Most of the strains belonging to the species Penicillium nalgiovense showed antagonistic activity in agar diffusion assays. Penicillium camemberti and Penicillium roqueforti strains proved to be inactive in these tests. The inhibitory substance excreted by P. nalgiovense strains was totally inactivated when treated with beta-lactamase (penicillinase), indicating that a beta-lactam antibiotic is produced by these strains. This observation was verified by PCRs with primer sets specific to the [delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine] synthetase gene (pcbAB), the isopenicillin-N-synthase gene (pcbC), and the acyl coenzyme A:6-aminopenicillanic acid acyltransferase gene (penDE) from Penicillium chrysogenum using chromosomal DNA of the fungal strains as a template. These results indicate that penicillin biosynthesis is a characteristic often found in strains of P. nalgiovense. No specific PCR signal could be identified with DNA from P. camemberti and P. roqueforti.
对用作食品发酵剂的青霉属特定菌株以及从霉菌发酵食品中分离出的菌株,分析它们抑制用作指示菌的藤黄微球菌DSM 348生长的能力。在琼脂扩散试验中,大多数属于纳氏青霉的菌株表现出拮抗活性。卡门青霉和罗克福青霉菌株在这些试验中被证明无活性。纳氏青霉菌株分泌的抑制物质在用β-内酰胺酶(青霉素酶)处理后完全失活,这表明这些菌株产生了一种β-内酰胺抗生素。使用真菌菌株的染色体DNA作为模板,通过针对产黄青霉的[δ-(L-α-氨基己二酰基)-L-半胱氨酰-D-缬氨酸]合成酶基因(pcbAB)、异青霉素-N-合成酶基因(pcbC)和酰基辅酶A:6-氨基青霉烷酸酰基转移酶基因(penDE)的引物对进行PCR验证了这一观察结果。这些结果表明青霉素生物合成是纳氏青霉菌株中常见的一个特征。用卡门青霉和罗克福青霉的DNA未鉴定出特异性PCR信号。