Eyssen H, Verhulst A
Appl Environ Microbiol. 1984 Jan;47(1):39-43. doi: 10.1128/aem.47.1.39-43.1984.
Eubacterium lentum is a gram-positive, nonsporeforming, nonmotile, asaccharolytic anaerobe. In the present investigations, 3 E. lentum strains (group E) isolated from rat feces were compared with 30 E. lentum strains (groups A, B, C, and D) previously studied by Macdonald et al. (I. A. Macdonald, J. F. Jellet, D. E. Mahony, and L. V. Holdeman, Appl. Environ. Microbiol. 37:992-1000, 1979). All strains alkalized (pH 8 to 8.5) arginine-containing (2 to 15 mg/ml) culture media, and growth of the majority of the strains was stimulated by arginine. All strains converted linoleic acid into transvaccenic acid by shifting the 12,13-cis double bond of linoleic acid into an 11,12-trans(?) double bond followed by biohydrogenation of the 9,10-cis double bond. Hence, biohydrogenation of linoleic acid is a new general characteristic of E. lentum. The 33 strains were also studied for bile acid deconjugase and hydroxysteroid dehydrogenase (HSDH) activities. The 6 strains in group D were steroid inactive; the 27 strains in groups A, B, C, and E were steroid active. The steroid-active group contained bile acid deconjugase-producing strains (groups C and E, plus strain 116 in group A) and nondeconjugating strains. All nondeconjugating strains of groups A and B developed 7 alpha- and 12 alpha-HSDH activities and contained 3 alpha-HSDH-positive strains and 3 alpha-HSDH-negative strains. Deconjugating strains varied in HSDH activities.
迟缓真杆菌是一种革兰氏阳性、不形成芽孢、无运动性、不分解糖类的厌氧菌。在本研究中,将从大鼠粪便中分离出的3株迟缓真杆菌菌株(E组)与Macdonald等人(I. A. Macdonald、J. F. Jellet、D. E. Mahony和L. V. Holdeman,《应用与环境微生物学》37:992 - 1000,1979年)之前研究的30株迟缓真杆菌菌株(A、B、C和D组)进行了比较。所有菌株都会使含精氨酸(2至15毫克/毫升)的培养基碱化(pH值为8至8.5),并且大多数菌株的生长受到精氨酸的刺激。所有菌株通过将亚油酸的12,13 - 顺式双键转变为11,12 - 反式(?)双键,随后对9,10 - 顺式双键进行生物氢化,将亚油酸转化为反式vaccenic酸。因此,亚油酸的生物氢化是迟缓真杆菌的一个新的普遍特征。还对这33株菌株的胆汁酸脱共轭酶和羟基类固醇脱氢酶(HSDH)活性进行了研究。D组的6株菌株无类固醇活性;A、B、C和E组的27株菌株有类固醇活性。有类固醇活性的组包含产生胆汁酸脱共轭酶的菌株(C组和E组,以及A组中的116号菌株)和不产生脱共轭酶的菌株。A组和B组的所有不产生脱共轭酶的菌株都具有7α - 和12α - HSDH活性,并且包含3α - HSDH阳性菌株和3α - HSDH阴性菌株。产生脱共轭酶的菌株在HSDH活性方面存在差异。