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. 2016 Jul 21;14(7):137. doi: 10.3390/md14070137

Table 1.

Realisation of biotechnological approaches for natural product antibiotics from marine fungi, listing all available literature until March 2016. Parameters and fermentation scale were indicated, if available. The origin was stated as concrete as obtained from literature. Abbreviations: Ref., References; EMF, Erlenmeyer flask; STR, stirred tank reactor; MR, Methicillin-Resistant; DSP, Downstream Processing.

Compound, Chemical Class Producer, Origin Biotechnological Approach Antibiotic Activity Against Ref.
15G265α,β,γ macrocyclic polylactones and lipodepsipeptide Hypoxylon oceanicum LL‑15G256, mangrove Optimised medium to increase titres
Effect of seawater (negative at low temperature)
Transfer to Fernbach flasks and 300-L fermenter
Staphylococcus epidermidis, Xanthomonas campestris Propionibacterium acnes [38,42]
Ascochytatin, spirodioxynaphthalene Ascochyta sp. NGB4, floating scrap of festering rope collected at a fishing port Optimisation of medium at small scale Bacterial two-component regulatory system [39]
Ascosetin, tetramic acid Lindgomycetaceae, Halichondria panicea, (sponge from Baltic Sea) Transfer from EMF to STR (10 L): adaptation of medium, increase of yield (factor 100) and decrease of cultivation time S. epidermidis, S. aureus, MR S. aureus, P. acnes, X. campestris, Septoria tritici [40]
Bis(2-ethylhexyl)phthalate, phthalate * Cladosporium sp., sea water in mangrove area Transfer from EMF to STR
Record of conditions
Scaling (2-L fermenter)
Loktanella hongkongensis, M. luteus, Rhodovulum sp., Ruegeria sp., Pseudoalteromonas piscida, Vibrio harveyi [41,51]
Calcarides A–E, macrocyclic and linear polyesters Calcarisporium sp., Wadden sea water Biosynthesis study for strain characterisation
Biological derivatisation
For calcaride A: Adaptation of medium in flasks (13‑fold improvement)
STR: 200-fold improvement by pH adaptation, C/N ratio, nature of mycelial growth
Macrocyclic compounds: S. epidermidis, X. campestris linear polyesters: no antibiotic activity [42,52]
Cephalosporin, β-lactam Aspergillus chrysogenum, sewage water Full fermentative optimised process, titres up to 25 g/L
Semi-synthesis from 7‑aminocephalosporanic acid (enzymatic)
Genetic engineering to reduce by‑products
Enzymatic treatment in DSP
Immobilised cells in a repeated batch tower reactor
Broad spectrum [43]
Cephalosporium chrysogenum, sea water DNA modified by mutagenesis Broad spectrum [53]
3-Chloro-2,5-dihydroxy benzyl alcohol, benzene derivative Ampelomyces sp., marine biofilm Scaling in EMF Micrococcus sp., Vibrio sp., Pseudoalteromonas sp., S. aureus, S. haemolyticus [37]
Chrysogenazine, diketopipera­zine Penicillium chrysogenum, Porteresia coarctata (mangrove plant, leaves) Scaling from 1-L to 5-L flasks
Yield of the compound enhanced by modifying the carbon and nitrogen source
Vibrio cholera [44]
Corollosporin and derivates, phthalide derivatives Corollospora maritima, marine driftwood Biological derivatives by enzymatic treatment
Salt dependency of fermentation
Candida maltosa, Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, S. aureus, S. aureus North German epidemic strain, S. epidermidis, S. haemolyticus [45,54]
Cyclo-(Pro-Phe), diketopiperazine Unidentified marine fungus UST030110-009, marine biofilm Scaling in EMF Antibacterial antibiofilm: Micrococcus sp., Vibrio sp., Pseudoalteromonas, S. aureus, S. haemolyticus [37]
Enniatins, cyclodepsipeptides Halosarpheia sp., mangrove Heterologous reprogramming of biosynthetic pathways E. coli, Enterococcus faecium, Salmonella enterica, Shigella dysenteriae, Listeria monocytogenes, Yersinia enterocolitica, Clostridium perfringens, P. aeruginosa, S. aureus [47]
Exophilin A, 3,5-dihydroxy-decanoic polyester Exophiala pisciphila, Mycale adhaerens (sponge) Transfer from EMF to STR (glass bottle fermenter, 20 L) E. facium, E. faecalis, S. aureus, MR S. aureus [48]
Lindgomycin, tetramic acid Lindgomycetaceae, Halichondria panicea (sponge from Baltic Sea) Adaptation of medium
Transfer from EMF to STR (10 L): increase of yield (factor 100) and decrease of cultivation time (from 14 to 7 days)
MR S. aureus, S. epidermidis, P. acnes, X. campestris, S. tritici [40]
Obioninene, ortho-quinone Leptosphaeria oraemaris, marine driftwood Effect of salinity on antibiotic production (in EMF) Fucus-associated not identified bacterium [49]
(+)-Terrein, cyclopentenone Aspergillus terreus PF-26, Phakellia fusca (sponge) Optimisation of operating factors (5-L STR) such as inoculation, agitation speed, aeration rate, pH control and nutrient feeding B. subtilis [55]
Not determined, sesterterpenoid Fusarium heterosporum and Aspergillus versicolor, driftwood and alga Metabolic engineering Broad spectrum [56]
Not determined Arthrinium c.f. saccharicola, seawater from a mangrove habitat Co-culture
Stimulation with bacterial elucidators
Systematic manipulation of culture conditions: salinity, temperature, pH, and culture medium composition
Pseudoalteromonas spongiae, Vibrio vulnificus [57]
Not determined Obligate fungi, marine deep-sea habitats High pressure cultivation
Scaling 20–100 L
Broad spectrum [58]

* Although bis(2-ethylhexyl)phthalate is a common plasticizer, its total amount was about 20% of the total fungal extract while hardly any plasticware was used during isolation. It was, therefore, assumed that bis(2-ethylhexyl)phthalate was truly produced by the fungus [41].