Production of poly(L-lactide)-degrading enzyme by Amycolatopsis orientalis for biological recycling of poly(L-lactide)

Appl Microbiol Biotechnol. 2006 Oct;72(4):726-31. doi: 10.1007/s00253-006-0343-4. Epub 2006 Feb 14.

Abstract

Efficient production of poly(L-lactide)(PLA)-degrading enzyme was achieved by addition of 0.1% (w/v) silk fibroin powder into a liquid culture medium of an actinomycete, Amycolatopsis orientalis, without other complex nitrogen sources, such as yeast extract and peptone. Scaled-up production of the enzyme in a 5-l jar fermenter showed the possibility of producing this enzyme on an industrial scale at low production cost. The extracellular PLA-degrading enzyme showed potent degrading activity, which is effective for biological recycling of PLA, i.e., 2,000 mg/l of PLA powder was completely degraded within 8 h at 40 degrees C using 20 mg/l purified enzyme. An optically active L-lactic acid with 600 mg/l was obtained as degradation product of PLA without undesirable racemization.

MeSH terms

  • Actinomycetales / enzymology*
  • Actinomycetales / growth & development
  • Carboxylic Ester Hydrolases / chemistry
  • Carboxylic Ester Hydrolases / isolation & purification
  • Carboxylic Ester Hydrolases / metabolism*
  • Conservation of Natural Resources
  • Culture Media / chemistry
  • Polyesters / metabolism*

Substances

  • Culture Media
  • Polyesters
  • poly(lactide)
  • Carboxylic Ester Hydrolases