In the paper by Matsumoto et al. 1, some text in the Results and Discussion sections appeared incorrectly: Sec signal should have read Tat signal. The correct text appears below:
Results
Based on SignalP prediction, the N‐terminal sequence of the active form of the enzyme starts at Thr28 of the deduced aa sequence, indicating that the preceding 27‐aa residues represent a Tat signal peptide sequence containing a twin‐arginine translocation (Tat) pathway motif (S/T‐R‐R‐X‐Hyd‐Hyd) that is required for secretion (Fig. 2).
Discussion
The signal peptide of LyPls‐PLD had a typical Tat signal sequence, suggesting that it should be secreted via the secretory pathway (Tat‐system secretion) [22].
In addition, reference [22] should be:
22 Lee PA, Tullman‐Ercek D and Georgiou G (2006) The bacterial twin‐arginine translocation pathway. Ann Rev Microbiol 60, 373–395. http://doi.org/10.1146/annurev.micro.60.080805.142212.
Reference
- 1. Matsumoto Y, Kashiwabara N, Oyama T, Murayama K, Matsumoto H, Sakasegawa S‐I and Sugimori D (2016) Molecular cloning, heterologous expression, and enzymatic characterization of lysoplasmalogen‐specific phospholipase D from Thermocrispum sp. FEBS Open Bio 6, 1113–1130. doi: 10.1002/2211‐5463.12131. [DOI] [PMC free article] [PubMed] [Google Scholar]