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bxzc123

金虫 (正式写手)

[求助] a为α,b为β生物名词实在看不懂求帮忙

Based on these facts,Yan et al. [31] reported the microbial transformation of 3-hydroxy-5,6-cyclopropanocholestanes-an alter route to 6-methylsteroids.
Incubation of 3b-hydroxy-5, 6 a -cyclopropano-5 a -cholestane (6)with Mycobacterium sp. (NRRL B-3805) gave three metabolites, 5,6 a -cyclopropano-5 a -androsta-3, 17-dione (7), 3b-hydroxy-5,6 a -cyclopropano-5 a -androsta-17-one (8) and androsta-4-ene-3,17-dione (5). Fermentation of 3b-hydroxy-5, 6b-cyclopropano-5b-
cholestane (9) with Mycobacterium sp. afforded the metabolite 5,5, 6b-cyclopropano-5b-androsta-3, 17-dione (10) and 3 a -hydroxy-5, 6b-cyclopropano-5b-androsta-17-one (11). Similarly, incubationof 3b-hydroxy-5, 6 a -cyclopropano-5 a -cholest-7-ene (12) with Mycobacterium sp. yielded a mixture of side chain cleaved 17-keto steroids as the major products, viz. the cyclopropyl eliminated product 5, 5, 6 a -cyclopropano-5 a -androst-7-ene-3, 17-dione (13),
3b-hydroxy-5, 6 a -cyclopropano-5 a -androst-4-ene-17-one (14), 5,
6 a -cyclopropano-5 a -androst-8(14)-ene-3, 7, 17-trione (15), 5,
6 a -cyclopropano-5 a -androst-8-ene-3, 7, 17-trione (16) and 6 a ,
7 a -cyclopropanoandrost-4-ene-3, 17-dione (17) as described in
Scheme 2.
a为α,b为β

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bxzc123

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2楼: Originally posted by ssssllllnnnn at 2015-04-22 21:25:07
Based on these facts,Yan et al.  reported the microbial transformation of 3-hydroxy-5,6-cyclo propano cholestane-an alter route to 6-methyl steroids. Incubation of 3β-hydroxy-5, 6 α-cyclo propano-5 ...

The fermentation yielded one reduced product: 17β-hydroxyandrost-1,4-dien-3-one and two hydroxylated
metabolites: 11α-hydroxyandrost-1,4-diene-3,17-dione and 12β-hydroxyandrost-1,4-diene-3,17-dione.怎么解释求帮忙
3楼2015-04-23 21:22:41
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ssssllllnnnn

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【答案】应助回帖

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bxzc123: 金币+100, 翻译EPI+1, ★★★很有帮助 2015-04-23 21:21:54
Based on these facts,Yan et al. [31] reported the microbial transformation of 3-hydroxy-5,6-cyclo propano cholestane-an alter route to 6-methyl steroids. Incubation of 3β-hydroxy-5, 6 α-cyclo propano-5 α-cholestane (6)with Mycobacterium sp. (NRRL B-3805) gave three metabolites, 5,6 α-cyclo propano-5 α-androsta-3, 17-dione (7), 3β-hydroxy-5,6 α-cyclo propano-5 α-androsta-17-one (8) and androsta-4-ene-3,17-dione (5). Fermentation of 3β-hydroxy-5, 6β-cyclo propano-5β-cholestane (9) with Mycobacterium sp. afforded the metabolite 5,5, 6β-cyclo propano-5β-androsta-3, 17-dione (10) and 3 α-hydroxy-5, 6β-cyclo propano-5β-androsta-17-one (11). Similarly, incubation of 3β-hydroxy-5, 6 α-cyclo propano-5 α-cholest-7-ene (12) with Mycobacterium sp. yielded a mixture of side chain cleaved 17-keto steroids as the major products, viz. the cyclopropyl eliminated product 5, 5, 6 α-cyclo propano-5 α-androst-7-ene-3, 17-dione (13), 3β-hydroxy-5, 6α-cyclo propano-5α-androst-4-ene-17-one (14), 5, 6 α-cyclo propano-5 α-androst-8(14)-ene-3, 7, 17-trione (15), 5, 6 α-cyclo propano-5 α-androst-8-ene-3, 7, 17-trione (16) and 6α, 7α-cyclo propano androst-4-ene-3,17-dione (17) as described in Scheme 2.

基于这些事实,Yan等【[31】报道的3-羟基-5,6-环丙醇胆甾烷微生物转化为6-甲基类固醇的不同途径。将3β羟基5,6α-环丙醇-5α-胆甾(6)与结核分枝杆菌(NRRL B-3805)孵育,得到3个代谢产物:5,6-α-环丙醇-5α-雄甾3,17二酮(7),3β羟基-5,6-α-环丙醇-5α-雄17酮(8)和雄甾-4-烯-3,17-二酮(5)。3β羟基-5-,6β-环丙醇-5β​​-胆甾(9)与结核分枝杆菌发酵,得到代谢物5,5,6β-环丙醇-5β​​-雄甾3,17二酮(10)和3α羟基-5,6β-环丙醇-5β​​-雄甾-17-酮(11)。类似地,如方案2中所述,3β羟基5,6α-环丙醇-5α-胆甾-7-烯(12)与结核分枝杆菌孵育,得到的主要产物是侧链17-酮类固醇侧链裂解混合物,即环丙基消除产物5,5,6α-环丙醇-5α-雄甾-7-烯-3,17-二酮(13),3β羟基-5,6α-环丙醇-5α-雄-4-烯-17酮(14),5,6α-环丙醇-5α-雄甾-8(14)-烯-3,7,17-三酮(15),5,6α-环丙醇-5-α-雄甾-8-烯-3,7,17三酮(16)和6α,7α-环丙醇,雄-4-烯-3,17-二酮(17)。
2楼2015-04-22 21:25:07
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