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Chemical structure and in vitro antitumor activity of rhamnolipids from Pseudomonas aeruginosa BN10

Appl Biochem Biotechnol. 2013 Jun;170(3):676-89. doi: 10.1007/s12010-013-0225-z. Epub 2013 Apr 19.

Abstract

A newly isolated indigenous strain BN10 identified as Pseudomonas aeruginosa was found to produce glycolipid (i.e., rhamnolipid-type) biosurfactants. Two representative rhamnolipidic fractions, RL-1 and RL-2, were separated on silica gel columns and their chemical structure was elucidated by a combination of nuclear magnetic resonance and mass spectroscopy. Subsequently, their cytotoxic effect on cancer cell lines HL-60, BV-173, SKW-3, and JMSU-1 was investigated. RL-1 was superior in terms of potency, causing 50 % inhibition of cellular viability at lower concentrations, as compared to RL-2. Furthermore, the results from fluorescent staining analysis demonstrated that RL-1 inhibited proliferation of BV-173 pre-B human leukemia cells by induction of apoptotic cell death. These findings suggest that RL-1 could be of potential for application in biomedicine as a new and promising therapeutic agent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology
  • BALB 3T3 Cells / drug effects
  • Cell Line, Tumor
  • Cell Survival
  • Glycolipids / chemistry
  • Glycolipids / isolation & purification*
  • Glycolipids / pharmacology
  • Humans
  • Lymphocytes / drug effects
  • Magnetic Resonance Spectroscopy
  • Mice
  • Pseudomonas aeruginosa / chemistry*
  • Spectrometry, Mass, Electrospray Ionization
  • Surface-Active Agents / chemistry
  • Surface-Active Agents / isolation & purification

Substances

  • Antineoplastic Agents
  • Glycolipids
  • Surface-Active Agents
  • rhamnolipid
  • rhamnolipid-1, Pseudomonas aeruginosa