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. Author manuscript; available in PMC: 2017 Sep 10.
Published in final edited form as: Appl Microbiol Biotechnol. 2009 May 20;84(3):535–544. doi: 10.1007/s00253-009-2024-6

Table 1.

Product distribution during degradation of RDX by purified XenA and XenB enzymes (average of duplicate assays) and by whole cells of P. putida II-B and P. fluorescens I-C (single replicates)

Assay RDX (μmol)
Products (μmol)
Mass balance (%)
Initial Residual MNX MEDINA NDAB HCHO C N
P fluorescens I-C 21.5 15.0 0.0   1.4 0.0 13.2   92 74
P putida II-B 21.5 11.7 0.0   0.4 0.3   2.7   60 56
XenB 69.1 29.2 0.0 37.4 0.0 82.2 100 78
XenA 69.1 28.9 0.2 23.5 1.5 76.1   98 66

Samples were collected for analysis after about half the initial RDX had been degraded (corresponding to approximately 100 and 400 h for whole cell assays with P. fluorescens I-C and P. putida II-B, respectively, and 4 and 24 h for XenB and XenA, respectively)