Liras Paloma, Demain Arnold L
Area de Microbiología, Facultad de Ciencias Biológicas y Ambientales, Universidad de León, León, Spain.
Methods Enzymol. 2009;458:401-29. doi: 10.1016/S0076-6879(09)04816-2.
Cephamycins are beta-lactam antibiotics with a cephem structure produced by actinomycetes. They are synthesized by a pathway similar to that of cephalosporin C in filamentous fungi but the actinomycetes pathway contains additional enzymes for the formation of the alpha-aminoadipic acid (AAA) precursor and for the final steps specific to cephemycins. Most of the biochemical and genetic studies on cephemycins have been made on cephemycin C biosynthesis in the producer strains Streptomyces clavuligerus ATCC27064 and Amycolatopsis lactamdurans NRRL3802. Genes encoding cephamycin C biosynthetic enzymes are clustered in both actinomycetes. Ten enzymatic steps are involved in the formation of cephamycin C. The precursor alpha-AAA is formed by the sequential action of lysine-6-aminotransferase and piperideine-6-carboxylate dehydrogenase. Steps common to cephalosporin C biosynthesis include the formation of the tripeptide L-delta-alpha-aminoadipyl-L-cysteinyl-D-valine (ACV) by ACV synthetase, the cyclization of ACV to form isopenicillin N (IPN) by IPN synthase, the epimerization of IPN to penicillin N by isopenicillin N epimerase, the ring expansion of penicillin N to a six member cephem ring by deacetoxycephalosporin C synthase (DAOCS) and the hydroxylation at C-3' by deacetylcephalosporin C hydroxylase. However, in actinomycetes, the epimerization step is different from that in cephalosporin-producing fungi, and the expansion of the ring and its hydroxylation are performed by separate enzymes. Specific steps in cephamycin biosynthesis include the carbamoylation at C-3' by cephem carbamoyl transferase and the introduction of a methoxyl group at C-7 by the joint action of a C-7 cephem-hydroxylase and a methyltransferase. All the enzymes of the pathway have been purified almost to homogeneity and the DAOC synthase and 7-hydroxycephem-methyltransferase (CmcI) of S. clavuligerus have been crystallized giving insights into the mode of action of these enzymes. The cefE gene of S. clavuligerus, encoding DAOCS, has been extensively used to expand the penicillin ring in filamentous fungi in vivo using DNA recombinant technology.
头霉素是由放线菌产生的具有头孢烯结构的β-内酰胺抗生素。它们的合成途径与丝状真菌中头孢菌素C的合成途径相似,但放线菌途径含有用于形成α-氨基己二酸(AAA)前体以及头霉素特有的最后步骤的额外酶。关于头霉素的大多数生化和遗传学研究都是针对产生菌链霉菌ATCC27064和产氨棒杆菌NRRL3802中头霉素C的生物合成进行的。编码头霉素C生物合成酶的基因在这两种放线菌中都是成簇的。头霉素C的形成涉及十个酶促步骤。前体α-AAA是由赖氨酸-6-转氨酶和哌啶-6-羧酸脱氢酶的顺序作用形成的。头孢菌素C生物合成的共同步骤包括由ACV合成酶形成三肽L-δ-α-氨基己二酰-L-半胱氨酰-D-缬氨酸(ACV),由IPN合酶将ACV环化形成异青霉素N(IPN),由异青霉素N差向异构酶将IPN差向异构化为青霉素N,由脱乙酰氧基头孢菌素C合酶(DAOCS)将青霉素N的环扩展为六元头孢烯环以及由脱乙酰头孢菌素C羟化酶在C-3'位进行羟基化。然而,在放线菌中,差向异构化步骤与产生头孢菌素的真菌中的不同,并且环的扩展及其羟基化是由不同的酶进行的。头霉素生物合成的特定步骤包括由头孢烯甲酰基转移酶在C-3'位进行氨甲酰化以及由C-7头孢烯羟化酶和甲基转移酶的共同作用在C-7位引入甲氧基。该途径的所有酶几乎都已纯化至同质,并且链霉菌的DAOC合酶和7-羟基头孢烯甲基转移酶(CmcI)已结晶,从而深入了解了这些酶的作用模式。链霉菌的cefE基因编码DAOCS,已被广泛用于利用DNA重组技术在丝状真菌体内扩展青霉素环。