Environmental control of the calicheamicin polyketide synthase leads to detection of a programmed octaketide and a proposal for enediyne biosynthesis.
Environmental control of the calicheamicin polyketide synthase leads to detection of a programmed octaketide and a proposal for enediyne biosynthesis.
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DOI:
10.1002/anie.201206462
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发表时间:
2012-11-05
影响因子:
16.6
通讯作者:
Townsend, Craig A.
中科院分区:
文献类型:
--
作者:
Belecki, Katherine;Townsend, Craig A.
The enediyne natural products exhibit potent antitumor and antibiotic activity in addition to displaying structural features that are quite remarkable both as a synthetic challenge and a biosynthetic enigma.[1] Members of this group typically incorporate a structural component designed for DNA recognition and a carbocyclic core containing an alkene (or masked alkene) flanked by triple bonds. It is this enediyne moiety that gives this class of compounds their name and their potent activity.As was foreshadowed by classical isotopic labeling studies,[2] biosynthetic gene cluster sequences for both 9-and 10-membered subclasses of enediynes confirm that the carbon skeletons of the enediyne core structures are made in nature by a family of type I iterative polyketide synthases (PKSs).[3] These multifunctional enzymes utilize a single set of domains to catalyze the repeated condensation and programmed reductive processing of activated malonyl units, analogous to mammalian fatty acid synthesis. In polyketide biosynthesis, however, the extent of processing in each round of two-carbon extension is controlled by the PKS, allowing for retention of ketones, hydroxyl groups, and double bonds into the growing polyketide chain. Intermediates remain covalently tethered to the PKS throughout the chain elongation process, complicating the investigation of these programming events.[4] Furthermore, the repeated use of a single set of domains in iterative systems often makes it difficult to predict the direct PKS product, particularly if it is highly modified en route to the final natural product.
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影响因子:
15
作者:
TOKIWA, Y;MIYOSHISAITOH, M;IWASAKI, S
通讯作者:
IWASAKI, S
影响因子:
15
作者:
Vagstad, Anna L.;Bumpus, Stefanie B.;Belecki, Katherine;Kelleher, Neil L.;Townsend, Craig A.
通讯作者:
Townsend, Craig A.
影响因子:
15
作者:
HENSENS, OD;GINER, JL;GOLDBERG, IH
通讯作者:
GOLDBERG, IH
DOI:
10.1073/pnas.0711625105
发表时间:
2008-02-05
影响因子:
11.1
作者:
Zhang, Jian;Van Lanen, Steven G.;Shen, Ben
通讯作者:
Shen, Ben
影响因子:
56.9
作者:
Liu, W;Christenson, SD;Shen, B
通讯作者:
Shen, B