Analysis of E‐IDSs from Mycobacterium species has clarified their functions: Mv0992 and Mv1577 would be E‐C₄₅ and E‐C₂₀ synthases, respectively; Mv3536 (an E‐C_10–20 synthase) released an E‐C₁₀ intermediate during continuous condensation; Rv0562 and Rv2173 had similar functions to Mv0992 and Mv3536, respectively; and reduced allylic diphosphate could be used as a substrate for Z‐IDS (Mv3822).

中文翻译：

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通过功能分析范巴伦分枝杆菌和结核分枝杆菌的异戊二烯基二磷酸合酶对类异戊二烯生物合成的了解。

对来自分枝杆菌属物种的E- IDS的分析已阐明其功能：Mv0992和Mv1577分别为E- C ₄₅和E- C ₂₀合酶。Mv3536（E C _10-20合酶）在连续缩合过程中释放出E C ₁₀中间体；Rv0562和Rv2173分别具有与Mv0992和Mv3536类似的功能；还原的烯丙基二磷酸酯可用作Z- IDS（Mv3822）的底物。