Al.pone.0061363.gbacteria can become more filamentous [36]. Numerous bacteria alter their shapes in response to the types and concentrations of internal and external compounds. For example, the E. coli DH5a strain forms long filamentous cells upon caffeine exposure [37], while over-production of penicillin-binding protein 2 causes morphological changes and lysis in E. coli [38]. Nutritional stress most frequently induces filamentation, which can increase the total surface area of a bacterium without increasing its width; hence its surface-to-volume ratio does not change [39]. In this study, the transformed E. coli strains changed their general morphology from short rods to filamentous structures (Figure 7), a change similar to bacteria encountering nutritional stress [39]. These changes occurred gradually over time (data not shown) and were not caused by IPTG addition alone, because IPTG induction over 6 h caused no such morphological changes in the WT strain (Figure 7A ). Furthermore, when fresh medium with or without IPTG was added to the 6-h induced cultures, the cells neither increased nor decreased in length when IPTG was included in the fresh medium, but they gradually shortened over several hours when IPTG was absent from the fresh medium (data not shown), suggesting that nutritional stress did not cause the changes in morphology. Perhaps the rapid accumulation of overexpressed proteins or FAs altered the cell shape. To some extent, cell size was related to the size of exogenous proteins produced. For example, GST transformants that produced ,27 kDa proteins had cell 
sizes about 1.5 times those of their uninduced counterparts (Table 2). In contrast, AhDGAT2a ST and AhDGAT2b ST transformants (expressing 64 kDa AhDGAT2 ST fusion proteins) increased their sizes by about 2.4?2.5 times that of their uninduced counterparts (Figure 7E , G?H). Apparently, the larger the size of the exogenous protein, the larger the transformed cell will become.IPTG induction and FA content in E. coliZhang et al. examined the effect of IPTG concentration on free FA accumulation and found that total free FA accumulation responded in a dosage-dependent way up to 500 mM of IPTG [35]. Below 500 mM, the cultures accumulated similar quantities of free FAs [35]; above this value, the percentages of the C14 and C16:1 straight chain FAs increased markedly, whereas the percentages of C16 and C18 fell dramatically [35]. In our study, IPTG affected FA accumulation in 1662274 E. coli. The cellular content of the individual FAs 194423-15-9 differed dramatically between the un-induced and induced cultures (Figure 8). The C12:0, C14:0, C18:3n3, and C21:0 cell contents increased significantly, whereas the C16:0, C16:1, and C18:1n9c contents decreased significantly. Furthermore, the transformants with AhDGAT2a and AhDGAT2bAhDGAT2-transformed E. coli strains would increase with longer induction times, but our study clearly demonstrated the potential of AhDGAT2 for efficient 10457188 FA production in E. coli.Overexpression of AhDGAT2 in E. coli changed its morphologyBacteria have evolved sophisticated systems to maintain their morphologies. However, in certain environments, rod-shapedTable 2. Cell sizes (mean6SE) of the MedChemExpress Oltipraz recombinant Escherichia coli strains.WT strain Uninduced cells width ( mm) length ( mm) volume ( mm3) Induced cells (6 h) width ( mm) length ( mm) volume ( mm3) 4.1060.12 27.19864.90 358.90661.57 4.1160.13 27.41264.23 361.73653.Empty vector 4.0860.14 25.91363.42 341.95642.91 4.1260.14 41.Al.pone.0061363.gbacteria can become more filamentous [36]. Numerous bacteria alter their shapes in response to the types and concentrations of internal and external compounds. For example, the E. coli DH5a strain forms long filamentous cells upon caffeine exposure [37], while over-production of penicillin-binding protein 2 causes morphological changes and lysis in E. coli [38]. Nutritional stress most frequently induces filamentation, which can increase the total surface area of a bacterium without increasing its width; hence its surface-to-volume ratio does not change [39]. In this study, the transformed E. coli strains changed their general morphology from short rods to filamentous structures (Figure 7), a change similar to bacteria encountering nutritional stress [39]. These changes occurred gradually over time (data not shown) and were not caused by IPTG addition alone, because IPTG induction over 6 h caused no such morphological changes in the WT strain (Figure 7A ). Furthermore, when fresh medium with or without 
IPTG was added to the 6-h induced cultures, the cells neither increased nor decreased in length when IPTG was included in the fresh medium, but they gradually shortened over several hours when IPTG was absent from the fresh medium (data not shown), suggesting that nutritional stress did not cause the changes in morphology. Perhaps the rapid accumulation of overexpressed proteins or FAs altered the cell shape. To some extent, cell size was related to the size of exogenous proteins produced. For example, GST transformants that produced ,27 kDa proteins had cell sizes about 1.5 times those of their uninduced counterparts (Table 2). In contrast, AhDGAT2a ST and AhDGAT2b ST transformants (expressing 64 kDa AhDGAT2 ST fusion proteins) increased their sizes by about 2.4?2.5 times that of their uninduced counterparts (Figure 7E , G?H). Apparently, the larger the size of the exogenous protein, the larger the transformed cell will become.IPTG induction and FA content in E. coliZhang et al. examined the effect of IPTG concentration on free FA accumulation and found that total free FA accumulation responded in a dosage-dependent way up to 500 mM of IPTG [35]. Below 500 mM, the cultures accumulated similar quantities of free FAs [35]; above this value, the percentages of the C14 and C16:1 straight chain FAs increased markedly, whereas the percentages of C16 and C18 fell dramatically [35]. In our study, IPTG affected FA accumulation in 1662274 E. coli. The cellular content of the individual FAs differed dramatically between the un-induced and induced cultures (Figure 8). The C12:0, C14:0, C18:3n3, and C21:0 cell contents increased significantly, whereas the C16:0, C16:1, and C18:1n9c contents decreased significantly. Furthermore, the transformants with AhDGAT2a and AhDGAT2bAhDGAT2-transformed E. coli strains would increase with longer induction times, but our study clearly demonstrated the potential of AhDGAT2 for efficient 10457188 FA production in E. coli.Overexpression of AhDGAT2 in E. coli changed its morphologyBacteria have evolved sophisticated systems to maintain their morphologies. However, in certain environments, rod-shapedTable 2. Cell sizes (mean6SE) of the recombinant Escherichia coli strains.WT strain Uninduced cells width ( mm) length ( mm) volume ( mm3) Induced cells (6 h) width ( mm) length ( mm) volume ( mm3) 4.1060.12 27.19864.90 358.90661.57 4.1160.13 27.41264.23 361.73653.Empty vector 4.0860.14 25.91363.42 341.95642.91 4.1260.14 41.
