Skip to main content
. 2015 Nov 6;10(11):e0142322. doi: 10.1371/journal.pone.0142322

Table 3. Expression values of gene clusters putatively involved in trehalose biosynthesis and polyphosphate degradation in P. putida LS46 under mcl-PHA permissive vs non-permissive conditions in WG cultures.

WG
(Sta vs Exp)
Locus-tag Gene symbol Gene product Expression abundance a Differential expression b
(PPUTLS46_)
RNA Protein Rnet Pnet
012110 glgA glycogen synthase - c - - -
012115 treY Malto-oligosyltrehalose trehalohydrolase - - - -
012120 malQ 4-alpha-glucanotransferase 9.94 19.10 -0.07 2.06
012125 treZ maltooligosyl trehalose synthase - - - -
012130 * protein of unknown function 8.98 20.04 -0.07 0.06
012135 glgX glycogen debranching protein - - - -
012140 hypothetical protein 9.07 - -0.44 -
012145 outer membrane autotransporter 7.34 - 0.99 -
012150 glgB* glycogen branching enzyme 11.34 19.80 -0.42 1.21
012155 treS trehalose synthase 9.95 21.02 -0.59 2.76
012160 alpha amylase family protein 10.19 20.09 -0.9 1.28
002907 treS trehalose synthase (Pseudomonas stutzeri type) 7.66 - 0.11 -
005431 glgP glycogen phosphorylase 11.14 22.36 -0.47 2.45

a Log2 expression abundance of gene products (mRNA and Protein) of P. putida LS46 grown under mid-log phase of waste glycerol culture (non-mcl-PHA synthesis condition). Values were averaged from two biological replicates

b Differential expression value of gene products under the specific comparing conditions: Sta, Stationary phase; Exp, Exponential phase; Significantly up-regulated proteins are indicated in bold

c a “-” symbol means not detected mRNA and/or protein expression under mid-log phase of WG culture and stationary culture of WG culture

* symbol indicates proteins (if detected) with S/N (signal to noise) ratio less than 2.8, and thus having FDR greater than 10%.