Surfactants tailored by the class Actinobacteria

被引:47
作者
Kuegler, Johannes H. [1 ]
Le Roes-Hill, Marilize [2 ]
Syldatk, Christoph [1 ]
Hausmann, Rudolf [3 ]
机构
[1] Karlsruhe Inst Technol, Inst Proc Engn Life Sci, Tech Biol, D-76131 Karlsruhe, Germany
[2] Cape Peninsula Univ Technol, Inst Biomed & Microbial Biotechnol, Biocatalysis & Tech Biol Res Grp, Bellville, South Africa
[3] Univ Hohenheim, Bioproc Engn, Inst Food Sci & Biotechnol, Stuttgart, Germany
关键词
biosurfactant; emulsifier; glycolipid; lipopeptide; trehalose lipid; Rhodococcus; rhamnolipid; LIPOARABINOMANNAN-LIKE LIPOGLYCAN; LEUKEMIA-CELL LINE; GLYCOLIPID BIOSURFACTANT; STREPTOMYCES-ROSEOSPORUS; ASTONISHING DIVERSITY; NATURAL SURFACTANTS; STRUCTURAL-CHARACTERIZATION; STRUCTURE ELUCIDATION; ACTIVE LIPIDS; GENE-CLUSTER;
D O I
10.3389/fmicb.2015.00212
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Globally the change towards the establishment of a bio-based economy has resulted in an increased need for bio-based applications. This, in turn, has served as a driving force for the discovery and application of novel biosurfactants. The class Actinobacteria represents a vast group of microorganisms with the ability to produce a diverse range of secondary metabolites, including surfactants. Understanding the extensive nature of the biosurfactants produced by actinobacterial strains can assist in finding novel biosurfactants with new potential applications. This review therefore presents a comprehensive overview of the knowledge available on actinobacterial surfactants, the chemical structures that have been completely or partly elucidated, as well as the identity of the biosurfactant-producing strains. Producer strains of not yet elucidated compounds are discussed, as well as the original habitats of all the producer strains, which seems to indicate that biosurfactant production is environmentally driven. Methodology applied in the isolation, purification and structural elucidation of the different types of surface active compounds, as well as surfactant activity tests, are also discussed. Overall, actinobacterial surfactants can be summarized to include the dominantly occurring trehalose-comprising surfactants, other non-trehalose containing glycolipids, lipopeptides and the more rare actinobacterial surfactants. The lack of structural information on a large proportion of actinobacterial surfactants should be considered as a driving force to further explore the abundance and diversity of these compounds. This would allow for a better understanding of actinobacterial surface active compounds and their potential for biotechnological application.
引用
收藏
页数:23
相关论文
共 156 条
[1]   Diversity, abundance and natural products of marine sponge-associated actinomycetes [J].
Abdelmohsen, Usama Ramadan ;
Bayer, Kristina ;
Hentschel, Ute .
NATURAL PRODUCT REPORTS, 2014, 31 (03) :381-399
[2]  
[Anonymous], INT J SYSTEMATIC E 5
[3]   Production of new extracellular glycolipids by a strain of Cellulomonas cellulans (Oerskovia xanthineolytica) and their structural characterization [J].
Arino, S ;
Marchal, R ;
Vandecasteele, JP .
CANADIAN JOURNAL OF MICROBIOLOGY, 1998, 44 (03) :238-243
[4]   BACTERIAL CAROTENOIDS .38. C50-CAROTENOIDS .9. ISOLATION OF DECAPRENOXANTHIN MONOGLUCOSIDE AND DIGLUCOSIDE FROM AN ARTHROBACTER SP [J].
ARPIN, N ;
TROUILLOUD, M ;
LIAAENJE.S .
ACTA CHEMICA SCANDINAVICA, 1972, 26 (06) :2524-+
[5]  
Asselineau C, 1978, Prog Chem Fats Other Lipids, V16, P59, DOI 10.1016/0079-6832(78)90037-X
[6]  
Asselineau Jean, 1998, Frontiers in Bioscience, V3, pE164
[7]   ROLE OF INTERFERON IN THE AUGMENTED RESISTANCE OF TREHALOSE-6,6'-DIMYCOLATE-TREATED MICE TO INFLUENZA-VIRUS INFECTION [J].
AZUMA, M ;
SUZUTANI, T ;
SAZAKI, K ;
YOSHIDA, I ;
SAKUMA, T ;
YOSHIDA, T .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :835-843
[8]   Renaissance in antibacterial discovery from actinomycetes [J].
Baltz, Richard H. .
CURRENT OPINION IN PHARMACOLOGY, 2008, 8 (05) :557-563
[9]   Bioactive microbial metabolites -: A personal view [J].
Bérdy, J .
JOURNAL OF ANTIBIOTICS, 2005, 58 (01) :1-26
[10]  
Bérdy J, 2012, J ANTIBIOT, V65, P385, DOI [10.1038/ja.2012.27, 10.1038/ja.2012.54]