Waldvogel F A, Swartz M N
J Bacteriol. 1969 May;98(2):662-7. doi: 10.1128/jb.98.2.662-667.1969.
Actively growing aerobic and anaerobic bacteria were screened by a plate assay, with reconstituted guinea pig collagen as a substrate, for their ability to produce a collagenolytic factor. Collagenolytic activity was not demonstrated among the aerobic organisms tested, with the exception of one strain of Staphylococcus aureus (only when grown under anaerobic conditions). Collagenolytic activity, however, was detected in cultures of Clostridium tetani and Bacteroides species other than B. melaninogenicus. Collagenolytic activity of these organisms could be confirmed by measuring the amount of hydroxyproline liberated from the collagen gel during growth. Although collagenase production by Pseudomonas aeruginosa has been suggested in previous reports, our results were negative. An extracellular fraction of P. aeruginosa was able to hydrolyze a synthetic hexapeptide Cbz-glycyl-l-prolyl-glycyl-glycyl-l-prolyl-l- alanine, but was without detectable effect on reconstituted collagen.
通过平板试验,以重构的豚鼠胶原蛋白为底物,筛选生长活跃的需氧菌和厌氧菌产生胶原olytic因子的能力。在所测试的需氧菌中,除一株金黄色葡萄球菌外(仅在厌氧条件下生长时),未显示出胶原olytic活性。然而,在破伤风梭菌和除产黑色素拟杆菌外的拟杆菌属培养物中检测到了胶原olytic活性。这些微生物的胶原olytic活性可通过测量生长过程中从胶原凝胶中释放的羟脯氨酸量来证实。尽管先前的报告中曾提示铜绿假单胞菌可产生胶原酶,但我们的结果为阴性。铜绿假单胞菌的细胞外部分能够水解合成六肽Cbz-甘氨酰-L-脯氨酰-甘氨酰-甘氨酰-L-脯氨酰-L-丙氨酸,但对重构胶原蛋白无明显影响。