Biotechnology and biochemistry of marine natural products.
Marine ecosystems are a source of biologically active compounds,
many of which are currently in clinical use. With the goal of increasing
the availability and the chemical diversity of these important
compounds, more researchers are applying the tools of biotechnology to
the discovery and production of marine natural products. This review
summarizes the recent efforts made towards the characterization of the
biochemical pathways that result in the production of marine natural
products, with an emphasis on the work aimed at understanding the
enzymatic activity involved in the biosynthesis of marine natural
Key words: Marine biotechnology, Natural products, Polyketides, Diterpenes, Polyunsaturated fatty acids
El ecosistema marino tropical es una fuente de compuestos con actividad biologica de un valor incalculable. Son varias las iniciativas que ya estan en pie con el proposito de explorar tanto la diversidad biologica y quimica de los oceanos como el uso de compuestos de origen marino en el tratamiento de enfermedades mortales. Algunos de estos esfuerzos recientes se centran en el uso de las herramientas de la biotecnologia y la bioquimica para el descubrimiento de nuevos compuestos. Otras iniciativas buscan emplear la biotecnologia con el proposito de generar diversidad quimica alrededor de compuestos prometedores asi como para generar fuentes renovables para la produccion industrial de estos compuestos. Es evidente que el alcanzar estas metas ambiciosas requerira un conocimiento mas completo de los procesos enzimaticos y moleculares que dan pie a la produccion de compuestos activos en el ambiente marino. En este articulo se resumen los hallazgos mas recientes en la identificacion y caracterizacion de rutas enzimaticas de biosintesis de compuestos marinos con enfasis particular en el trabajo realizado con enzimas purificadas.
ADN (Analisis de casos)
Bioquimica (Investigacion cientifica)
Bioquimica (Analisis de casos)
Biotecnologia (Investigacion cientifica)
Biotecnologia (Analisis de casos)
Oceano (Investigacion cientifica)
Oceano (Analisis de casos)
|Publication:||Name: Puerto Rico Health Sciences Journal Publisher: Universidad de Puerto Rico, Recinto de Ciencias Medicas Language: Spanish Audience: Academic Format: Magazine/Journal Subject: Health Copyright: COPYRIGHT 2009 Universidad de Puerto Rico, Recinto de Ciencias Medicas ISSN: 0738-0658|
|Issue:||Date: Sept, 2009 Source Volume: 28 Source Issue: 3|
|Geographic:||Geographic Name: Puerto Rico|
Natural products isolated from marine samples have a wide spectrum
of biological activities and numerous therapeutic applications. Many
compounds with antiviral, antibiotic and anti-tumor activity have been
isolated from marine samples and tested in cell culture for their
ability to specifically target and kill pathogenic or cancerous cells by
disrupting diverse cellular processes (1-2). A number of these
compounds, or synthetic analogues based on natural compounds, have
entered clinical trials and some are currently administered as
Despite the great promise and the wide spectrum of biological activities of marine natural products, their subsequent development as therapeutic products has been slowed down due to several factors including the low availability of biologically active compounds (4), their high chemical complexity (5) and, in some cases, their high toxicity at therapeutic doses. Some compounds are produced by organisms which comprise only a minority component within the diverse population in the sample. In fact, many promising natural products associated with marine sponges and corals have been found not to be made by the invertebrate itself, but rather by symbiotic bacteria which are difficult to isolate, characterize and cultivate.
Several commercial ventures have been created precisely to apply the ethos of biotechnology to the development of marine drugs by devising ways to overcome some of the aforementioned difficulties in order to bring some of the more promising compounds closer to the clinic and to the market (6). Companies such as PharmaMar (Madrid, Spain) and Nereus Pharmaceuticals (San Diego, USA) have developed strategies for identifying cultivable organisms, optimizing growth, maximizing compound production, and increasing chemical diversity through synthetic modification (7) (Figure 1). This approach has yielded the first generation of biotechnology-derived marine natural products. PharmaMar currently makes and sells the natural anticancer compound trabectedin (Yondelis[R]), which is produced by a semi-synthetic method in which a natural fermentation product from Pseudomonas fuorescens is chemically modified to form the final product (8). Another biotech company developing marine drugs is Nereus Pharmaceuticals, which is currently conducting Phase I clinical trials for proteasome inhibitor, salinosporamide A, for the treatment of solid tumors, lymphomas and multiple myeloma (9). This active compound is isolated directly from the fermentation of marine actinomycete, Salinispora tropica, a species first identified and characterized at the Scripps Institution of Oceanography by Paul Jensen and William Fenical (10).
[FIGURE 1 OMITTED]
The successful application of biotechnology to the development of marine-derived pharmaceuticals has been met with an increased drive towards elucidating the enzyme pathways that lead to the biosynthesis of such complex and biologically active molecules. These recent efforts involve the cloning and characterization of multienzyme complexes, such as polyketide synthases (PKS) and non-ribosomal peptide synthetases (NRPS), terpene cyclases and halogenases (11-12). Additional efforts involve the mechanistic and structural characterization of some of these biosynthetic enzymes as well as their expression and activity in heterologous hosts. This review attempts to provide a general view of the recent work aimed at understanding the enzyme pathways involved in the biosynthesis of marine natural products.
Marine actinobacteria and salinosporamide A
Actinobacteria are a group of gram-positive, GC-rich bacteria which are well-known producers of biologically active compounds. Many antibiotics, immuno-suppressants and anticancer drugs are made from the cultivation of actinobacteria, many of them originally identified in tropical soils. The antibiotics erythromycin and rifamycin are still produced commercially from the fermentation cultures of soil actinobacteria.
Actinobacteria have also been found in marine sediments (10). Both Salinispora arenicola and Salinispora tropica are marine actinobacteria which were initially identified in sea sediments from the Bahamas. They both require seawater for cultivation and produce a number of natural products. In fact, analysis of the genome of S tropica reveals that approximately 9.9% of the DNA sequence is dedicated to the assembly of secondary metabolites (13). One of these secondary metabolites is Salinosporamide A, a potent inhibitor of the proteasome which is currently in Phase I clinical trials for the treatment of solid tumors, lymphomas and multiple myeloma.
The biosynthetic route to Salinosporamide A was proposed on the basis of feeding experiments in which S tropica in cell culture was fed labeled precursors, in this case acetate and shikimate (14). From the labeling pattern of the isolated final product the authors deduced the enzyme-catalyzed reactions that lead to its biosynthesis from three building blocks (Figure 2). It was proposed that a polyketide synthase (PKS) catalyzes the condensation of a chlorobutanoyl intermediate with an acetate unit, and subsequently with the clyclohexenyl-alanine amino acid arising from the shikimate pathway which is incorporated into the product by the activity of a non-ribosomal peptide synthetase (NRPS).
[FIGURE 2 OMITTED]
[FIGURE 3 OMITTED]
Based on this proposed biosynthetic pathway, a number of analogues of salinosporamide A have been generated using the tools of biotechnology (Figure 3). The inactivation of the Sal X gene, which is required for the biosynthesis of the amino acid, cyclohexenyl-alanine, resulted in the production of antiprotealide, a novel biologically active compound in which the amino acid leucine occupies the place of the original cyclohexenyl amino acid (15). Additionally, chemical complementation experiments in which other non-proteinogenic amino acids were fed to the SaIX- strain, resulted in the incorporation of the exogenous amino acids into the final product, thus demonstrating the capacity of a "mutasynthetic" approach for the discovery of new compounds not easily accessible by conventional chemical methods.
Enterocin and the reconstitution of biosynthetic pathways
The marine actinobacteria Streptomyces maritimus produces a diverse family of antibacterial compounds known as the enterocins and wailupemycins. These compounds are made by a Type 11 polyketide synthase (PKS) which catalyzes successive condesations of a benzoyl-CoA starter unit with seven malonyl-CoA building blocks by the proteins encA, encB, encC and encD (16). In an attempt to generate novel polyketides, the biosynthetic genes for the benzoyl-CoA starter unit in S maritimus were introduced into a streptomyces strain that produces truncated versions of erythromycin. The resulting Streptomyces strain produced novel PKS-derived triketides, containing the benzoate starter unit prescribed by the S maritimus genes (17). This result not only confirmed the tolerance of terrestrial Type I PKS toward alternative starter units, but also highlighted the enormous potential of using genes from a marine organism to modify known polyketides.
More recently, the entire biosynthetic pathway for enterocin was reconstituted in vitro from recombinantly expressed enzymes (18). While most enzymes were expressed inEscherichia coh, some enzymes were insoluble or inactive when expressed in that host. In those cases, the enzymes were overexpressed in well characterized hosts for the expression of streptomycete proteins, Streptomyces lividans or Streptomyces coelicolor. Efforts to reprogram the biosynthesis of enterocins and wailupemycins include the mutasynthesis of analogues of enterocin with non-natural starter units in which the authors fed aryl acids to a strain of S maritimus that was incapable of producing benzoate-primed polyketides. The result was a number of enterocin analogues with a different aryl starter unit (19). This general strategy has been taken a step further with the in vitro reconstituted enterocin enzyme complex (20). In this paper, Kalaitzis, et al. directly prime the corresponding biosynthetic enzyme with an alternative priming unit, other than the natural benzoate. The result is a number of novel enterocin and wailupemycin analogues obtained by means of recombinant technology.
Curacin biosynthesis in cyanobacteria
Cyanobacteria are another source of biologically active marine natural products many of which result from the activity of hybrid PKS:NRPS enzyme complexes (21). This is the case for hybrid molecules barbamide and curacin, both of which result from a biosynthetic route that includes both PKS domains and NRPS domains (22-23). The biosynthesis of barbamide, a molluscicidal compound, involves the condensation of three amino acids (trichloroleucine, phenylalanine and cysteine) with a malonate unit (Figure 4). The ability of the barbamide enzyme complex to specifically incorporate those amino acids has been confirmed in vitro using purified adenylation domains from the barbamide gene cluster over-expressed in E coli (22).
[FIGURE 4 OMITTED]
The biosynthesis of curacin, a potent anticancer compound from the cyanobacterium Lyngbya majuscula, involves the incorporation of a rare cyclopropyl moiety into the polyketide chain. The initial steps of this enzymatic transformation have been explored using two purified enzymes from the curacin gene cluster, CurE and CurF (24). Both sequences were found to align with the enoyl-CoA hydratase (ECH) family of enzymes which typically catalyze the hydration of double bonded intermediates during the beta-oxidation of fatty acids. Assays using purified enzymes showed that CurE catalyzes the dehydration of HMG-ACP while CurF catalyzes the subsequent decarboxylation to form the 3-methyl intermediate that gives rise to the cyclopropyl moiety. This work opens the possibility of using this CurE-CurF enzyme pair to engineer priming units for other PKS systems as a way to introduce cyclopropanes into known polyketide compounds.
Bryostatin in a symbiont of Bugula neritina
Marine bacteria are not the only source of biologically active natural products. There are many reports of natural products isolated from marine invertebrates. However, many of these natural products have been since found to be made not by the invertebrate animal but rather by a symbiotic microorganism. This is the case of bryostatin 1, a potent anticancer compound found in the organism Bugula neritina, a common and abundant member of the fouling community in harbors and bays. Studies to characterize the genes required for the biosynthesis of bryostatin 1 in B neritina revealed that the PKS genes required for the production of bryostatin 1 were located not in the bryozoan but rather in a symbiont Endobugula sertula (25).
[FIGURE 5 OMITTED]
The benefit of using DNA technology to enhance the production of marine drugs is particularly important in the case of a compound like bryostatin. Bryostatin is an inhibitor of protein kinase C and is currently in clinical trials for the treatment of various cancers, Alzheimers disease and strokes. Yet, the abundance of this polyketide in the producing organism is fairly low. In order to obtain 1 g of bryostatin, over 1500 pounds of B neritina are required. For this reason, finding the gene cluster responsible for the production of bryostatin in E sertula will be essential in the development of a sustainable source of this important compound.
A gene cluster for a Type I PKS has been cloned and sequenced in E sertula strains collected at both deep and shallow waters (26). The genes, named BryA,B,C,D and X, are the only large open reading frames in an otherwise degenerate genome and the only genes for Type I PKS found in E sertula, suggesting that they are, in all likelihood, responsible for the production of bryostatin (27). According to the proposed biosynthetic route for this compound, only BryA,B,C and D are necessary for building the polyketide backbone, while BryX is an inactive or seemingly superfluous gene. However, the fact that BryX is present in both deep and shallow strains together with the fact that RT PCR data shows transcription of the BryX gene, both suggest that the BryX gene is utilized by the organism.
Recently, the first biochemical evidence of biochemical activity in the bry gene cluster came from work with the bryP protein (28). BryP is a discrete acyltransferase domain which loads malonate units onto the ACP domains located in the elongation modules. This activity is required in this type of cluster because there is no acyltransferase present in the modular PKS. Results show BryP to be active against other ACP domains in "AT-less" PKS modules, as well as against excised ACP domains from other Type I PKS.
Pseudopterosins in corals
Pseudopterosins are diterpene molecules isolated from corals with anti-inflammatory and analgesic properties. These compounds have been found to significantly inhibit phorbol myristate acetate-induced topical inflammation in mice and the methyl ether of this natural product has shown promise as a treatment for contact dermatitis (29-30). They are made by the cyclization of geranylgeranyl diphosphate (GGPP) to form the intermediate elisabethatriene, which is in turn converted to a variety of final products (Figure 6). The enzyme that catalyzes such cyclization has been purified directly from the source organism and assayed for cyclase activity (31). The purified enzyme, the first diterpene cyclase from a marine organism ever characterized, has similar properties and kinetic parameters as other diterepene cyclases, such as pl, pH optimum, and Km.
In more recent work, the purified elisabethatriene synthase was challenged with alternative shorter substrates, geranyl diphosphate and famesyl diphosphate, resulting in the production of alternative diterpenes (32). This result highlights the potential application of this family of enzymes in the generation of novel compounds derived from known diterpene precursors.
[FIGURE 6 OMITTED]
Omega-3 Fatty Acids from deep-sea bacteria
Long chain omega-3 fatty acids are essential nutrients in the human diet. They are involved in brain and eye development as well as in the maintenance of good cardiovascular health (33-34). Most of the long chain omega-3 in human diet comes either directly from the consumption of oily fish or indirectly from the relatively inefficient elongation of the medium-chain omega-3 present in some vegetable oils. Fish, in turn, also have an inefficient mechanism for producing their own long-chain omega-3 and must obtain it from a diet rich in microalgae and bacteria, both major sources of these important nutrients.
The biosynthesis of omega-3 in deep-sea bacteria takes place not by the desaturation and elongation of saturated fatty acids, but rather by a polyunsaturated fatty acid (PUFA) synthase system which resembles a PKS in that it builds the fatty acid one acyl unit at a time, introducing the double bonds as the chain grows attached to an acyl carrier protein (35). The PUFA synthase genes have been identified in different organisms and the organization of genes within the clusters show some commonalities (3536) (Figure 7). For instance, all gene clusters for PUFA synthase sequenced so far have a number of between 4-6 ACP domains in tandem. Also, all PUFA synthase clusters dehydratase (DH) domains, presumed to be responsible for the formation of double bonds in the final product, are organized in pairs. This organization of DH domains is unlike that of DH domains normally found in modular PKS.
The PUFA synthase genes have been introduced into E coli, resulting in the production of omega-3 fatty acids in a heterologous host (37-39). These results indicated that PUFA synthase genes alone were all that was required for the biosynthesis of long-chain omega-3 in deep sea bacteria and that no elongase-desaturase enzyme was required. These results also highlight the potential of using E coli as a heterologous hosts for the production and for the expression of PUFA synthase proteins.
The biochemical activity of some of the PUFA synthase enzymes has also been reported. In order to determine how many of the tandem ACP domains are required for product assembly, the ACP domains from Shewanella japonica were systematically inactivated and expressed in E coli with the other components of the PUFA gene cluster (40). Results confirmed the presence of ACP domains that were functional as revealed by the fact that they are recognized as substrates for phosphopantetheinyl transferases (PPTases). More importantly, results showed fatty acids can still be produced if all but one ACP domain has been inactivated by mutagenesis. These results answer the question of how many ACP domains are required for product assembly, but it does not explain the prevalence of tandem ACP domains in all known PUFA clusters, while virtually absent in other modular PKS systems.
[FIGURE 7 OMITTED]
The activity of the enoyl reductase enzyme in the PUFA gene cluster, pfaD, has also been measured in vitro (41). In this first measurement of enzymatic activity of a purified PUFA synthase component, the pfaD was expressed, purified and assayed for its ability to catalyze the reduction of the 2-butenoyl-ACP, a predicted authentic intermediate of the reaction. High-resolution mass spectrometric measurements showed a 2 Da increase in the molecular weight of the holo ACP in the presence of NADPH, demonstrating that pfaD is indeed an enoyl reductase as had been predicted by sequence alignments.
Biotechnology is being applied successfully to the study of marine natural products and to their subsequent development as therapeutics. In the examples discussed in this review, the biosynthetic routes for some of the more interesting and promising marine compounds are studied by a combination of approaches which include genetics, bioorganic chemistry and enzyme biochemistry. Two underlying goals can be discerned from these efforts: 1) finding more sustainable and economically viable ways to produce marine compounds and 2) increasing the biochemical diversity of compound families. Biotechnology is driving the steady advancement of both of these goals as it promises to open doors in the quest for new medicines and new treatments.
Abbreviations and acronyms
PKS = Polyketide Synthases
NRPS = Non-ribosomal peptide synthetase
ACP = Acyl carrier protein
AT = Acyltransferase
PUFA = Polyunsaturated fatty acids
ECH = Enoyl CoA hydratase
GGPP = geranylgeranyl diphosphate
DH = dehydratase
PPTase = phosphopantetheinyl transferase
(1.) Fenical W. Marine biodiversity and the medicine cabinet. Oceanography 1996;9:23-27.
(2.) Munro MHG, Blunt JW, Dumdei EJ, Hickford SJH, Lill RE, Li S, Battershill CN, Duckworth AR. The discovery and development of marine compounds with pharmaceutical potential. J Biotech 1999 70:15-25.
(3.) Kijjoa A, Sawangwong P. Drugs and cosmetics from the sea. Mar Drugs 2004;2:73-82.
(4.) Schaufelberger DE, Koleck MP, Beutler JA, Vatakis AM, Alvarado AB, Andrews P, Marzo LV, Muschik GM, Roach J, Ross JT. The large-scale isolation of bryostatin 1 from bugula neritina following current good manufacturing practices. J Nat Prod 1991;54: 1265-1270.
(5.) Baryza JL, Brenner SE, Craske ML, Meyer T, Wender PA. Simplified analogs of bryostatin with anticancer activity display greater potency for translocation of PKCS-GFP. Chem Biol 2004; 11:1261-1267.
(6.) Haefner B. Drugs from the deep: Marine natural products as drug candidates. Drug Discovery Today 2003;8:536-544.
(7.) Gullo VP, Hughes DE. Exploiting new approaches for natural product drug discovery in the biotechnology industry. Drug Discovery Today: Technologies 2005;2:281-286.
(8.) Cuevas C, Perez M, Martin MJ, Chicharro JL, Fernandez-Rivas C, Flores M, Francesch A, Gallego P, Zarzuelo M, de 1C, Garcia J, Polanco C, Rodriguez I, Manzanares I. Synthesis of ecteinascidin ET-743 and phthalascidin pt-650 from cyanosafracin B. Org Lett 2000;2:2545-2548.
(9.) Fenical W, Jensen PR, Palladino MA, Lam KS, Lloyd GK, Potts BC. Discovery and development of the anticancer agent salino-sporamide A (NPI-0052). Bioorg Med Chem 2009;17:2175-2180.
(10.) Jensen PR, Dwight R, Fenical W. Distribution of actinomycetes in near-shore tropical marine sediments. Appl Environ Microbiol. 1991;57:1102-1108.
(11.) Eustaquio AS, Pojer F, Noel JP, Moore BS. Discovery and characterization of a marine bacterial SAM-dependent chlorinase. Nat Chem Biol 2008;4:69-74.
(12.) Eustaquio AS, Harle J, Noel JP, Moore BS. S-adenosyl-L-methionine hydrolase (adenosine-forming), a conserved bacterial and archeal protein related to SAM-dependent halogenases. ChemBioChem. 2008;9:2215-2219.
(13.) Udwary DW, Zeigler L, Asolkar RN, Singan V, Lapidus A, Fenical W, Jensen PR, Moore BS. Genome sequencing reveals complex secondary metabolome in the marine actinomycete salinispora tropica. Proc Natl Acad Sci U S A 2007; 104:10376-10381.
(14.) Beer LL, Moore BS. Biosynthetic convergence of salinosporamides A and B in the marine actinomycete salinispora tropica. Org Lett 2007;9:845-848.
(15.) McGlinchey RP, Nett M, Eustaquio AS, Asolkar RN, Fenical W, Moore BS. Engineered biosynthesis of antiprotealide and other unnatural salinosporamide proteasome inhibitors. J Am Chem Soc 2008;130:7822-7823.
(16.) Hertweck C, Xiang L, Kalaitzis JA, Cheng Q, Palzer M, Moore BS. Context-dependent behavior of the enterocin iterative polyketide synthase: A new model for ketoreduction. Chem Biol 2004;11:461-468.
(17.) Garcia-Bemardo J, Xiang L, Hong H, Moore BS, Leadlay PF. Engineered biosynthesis of phenyl-substituted polyketides. ChemBioChem 2004; 5:1129-1131.
(18.) Cheng Q, Xiang L, Izumikawa M, Meluzzi D, Moore BS. Enzymatic total synthesis of enterocin polyketides. Nat Chem Biol 2007;3:557-558.
(19.) Kalaitzis JA, Izumikawa M, Xiang L, Hertweck C, Moore BS. Mutasynthesis of enterocin and wailupemycin analogues. J Am Chem Soc 2003;125:9290-9291.
(20.) Kalaitzis JA, Cheng Q, Thomas PM, Kelleher NL, Moore BS. In vitro biosynthesis of unnatural enterocin and wailupemycin polyketides. J Nat Prod 2009;72:469-472.
(21.) Gerwick WH, Tan LT, Sitachitta N. Nitrogen-containing metabolites from marine cyanobacteria. Alkaloids Chem Biol 2001;57: 75-184.
(22.) Chang Z, Flatt P, Gerwick WH, Nguyen V, Willis CL, Sherman DH. The barbamide biosynthetic gene cluster: A novel marine cyanobacterial system of mixed polyketide synthase (PKS)-nonribosomal peptide synthetase (NRPS) origin involving an unusual trichloroleucyl starter unit. Gene 2002;296:235-247.
(23.) Chang Z, Sitachitta N, Rossi JV, Roberts MA, Flatt PM, Jia J, Sherman DH, Gerwick WH. Biosynthetic pathway and gene cluster analysis of curacin A, an antitubulin natural product from the tropical marine cyanobacterium lyngbya majuscula. J Nat Prod 2004;67:1356-1367.
(24.) Gu L, Jia J, Liu H, Hakansson K, Gerwick WH, Sherman DH. Metabolic coupling of dehydration and decarboxylation in the curacin A pathway: Functional identification of a mechanistically diverse enzyme pair. J Am Chem Soc 2006;128:9014-9015.
(25.) Davidson SK, Allen SW, Lim GE, Anderson CM, Haygood MG. Evidence for the biosynthesis of bryostatins by the bacterial symbiont "candidatus endobugula sertula" of the bryozoan bugula neritina. Appl Environ Microbiol 2001;67:4531-4537.
(26.) Sudek S, Lopanik NB, Waggoner LE, Hildebrand M, Anderson C, Liu H, Patel A, Sherman DH, Haygood MG. Identification of the putative bryostatin polyketide synthase gene cluster from "Candidatus endobugula sertula", the uncultivated microbial symbiont of the marine bryozoan bugula neritina. J Nat Prod 2007; 70:67-74.
(27.) Hildebrand M, Waggoner LE, Liu H, Sudek S, Allen S, Anderson C, Sherman DH, Haygood M. bryA: An unusual modular polyketide synthase gene from the uncultivated bacterial symbiont of the marine bryozoan bugula neritina. Chem Biol 2004;11: 1543-52.
(28.) Lopanik NB, Shields JA, Buchholz TJ, Rath CM, Hothersall J, Haygood MG, Hakansson K, Thomas CM, Sherman DH. In vivo and in vitro trans-acylation by BryP, the putative bryostatin pathway acyltransferase derived from an uncultured marine symbiont. Chem Biol 2008;15:1175-1186.
(29.) Look SA, Fenical W, Jacobs RS, Clardy J. The pseudopterosins: Anti-inflammatory and analgesic natural products from the sea whip pseudopterogorgia elisabethae. Proc Natl Acad Sci U S A 1986;83:6238-6240.
(30.) Haimes H, Glasson S, Harlan P, Jacobs R, Fenical W, Jimenez J. Pseudopterosin A methyl ester (OAS 1000): A novel non-steroidal anti-inflammatory. Inflammation Res 1995;44:13-17.
(31.) Kohl AC, Kerr RG. Identification and characterization of the pseudopterosin diterpene cyclase, elisabethatriene synthase, from the marine gorgonian, pseudopterogorgia elisabethae. Arch Biochem Biophys 2004;424:97-104.
(32.) Briick TB, Kerr RG. Purification and kinetic properties of elisabethatriene synthase from the coral pseudopterogorgia elisabethae. Comp Biochem Physiol B Biochem Mol Biol 2006;143:269-278.
(33.) Voigt RG, Jensen CL, Fraley JK, Rozelle JC, Brown FR, 3rd, Heird WC. Relationship between omega3 long-chain polyunsaturated fatty acid status during early infancy and neurodevelopmental status at 1 year of age. J Hum Nutr Diet 2002;15:111-120.
(34.) Burr ML, Fehily AM, Gilbert JF, Rogers S, Holliday RM, Sweetnam PM, Elwood PC, Deadman NM. Effects of changes in fat, fish, and fibre intakes on death and myocardial reinfarction: Diet and reinfarction trial (DART). Lancet 1989;2:757-61.
(35.) Metz JG, Roessler P, Facciotti D, Levering C, Dittrich F, Lassner M, Valentine R, Lardizabal K, Domergue F, Yamada A, Yazawa K, Knauf V, Browse J. Production of polyunsaturated fatty acids by polyketide synthases in both prokaryotes and eukaryotes. Science 2001;293:290-293.
(36.) Allen EE, Bartlett DH. Structure and regulation of the omega-3 polyunsaturated fatty acid synthase genes from the deep-sea bacterium photobacterium profundum strain SS9. Microbiology 2002; 148:1903-1913.
(37.) Orikasa Y, Yamada A, Yu R, Ito Y, Nishida T, Yumoto I, Watanabe K, Okuyama H. Characterization of the eicosapentaenoic acid biosynthesis gene cluster from shewanella sp. strain SCRC-2738. Cell Mol Biol (Noisy-le-grand) 2004;50:625-630.
(38.) Orikasa Y, Nishida T, Yamada A, Yu R, Watanabe K, Hase A, Morita N, Okuyama H. Recombinant production of docosahexaenoic acid in a polyketide biosynthesis mode in escherichia coli. Biotechnol Lett 2006;28:1841-1847.
(39.) Orikasa Y, Nishida T, Hase A, Watanabe K, Morita N, Okuyama H. A phosphopantetheinyl transferase gene essential for biosynthesis of n--3 polyunsaturated fatty acids from moritella marina strain MP-1. FEBS Letters 2006;580:4423-4429.
(40.) Jiang H, Zirkle R, Metz JG, Braun L, Richter L, Van Lanen SG, Shen B. The role of tandem acyl carrier protein domains in polyunsaturated fatty acid biosynthesis. J Am Chem Soc 2008;130:6336-6337.
41. Bumpus SB, Magarvey NA, Kelleher NL, Walsh CT, Calderone CT. Polyunsaturated fatty-acid-like trans-enoyl reductases utilized in polyketide biosynthesis. J Am Chem Soc 2008;130: 11614-11616.
ABEL BAERGA-ORTIZ, PhD
This work was supported by seed funding from the office of the Dean of the School of Medicine. The author has no conflict of interest to disclose.
Address correspondence to: Abel Baerga-Ortiz, Ph D, Assistant Professor, Department of Biochemistry, University of Puerto Rico Medical Sciences Campus, PO Box 365067, San Juan Puerto Rico 00936. Tel: 787-758-2525 ext. 1603 * Fax: 787-274-8724 * Email: firstname.lastname@example.org
|Gale Copyright:||Copyright 2009 Gale, Cengage Learning. All rights reserved.|