Graduate Program in Genomic Sciences and Biotechnology, Universidade Católica de Brasília, QS 07 Lote 01 Bloco G, Taguatinga, Brasília, DF 71966-700, Brazil.
Graduate Program in Biotechnology, Universidade Federal de Uberlândia, Patos de Minas. R. Padre Pavoni, 290, Patos de Minas, MG 38701-002, Brazil.
Lett Appl Microbiol. 2024 Sep 2;77(9). doi: 10.1093/lambio/ovae079.
Pelgipeptins, tridecaptins, and elgicins are among the antimicrobials produced by Paenibacillus elgii. Growth in complex media is commonly applied to obtain lipopeptides from culture's supernatant, but it requires further purification. This study aimed to improve the yield of pelgipeptins and tridecaptins using chemically defined media. The kinetics of antimicrobial lipopeptide yield in chemically defined media were evaluated in P. elgii AC13. Pelgipeptins were detected in the supernatant and the culture pellet, but tridecaptins were mainly associated with cell debris or endospores. We investigated whether removing Ca2+ would impair P. elgii sporogenesis, consequently improving the yield of tridecaptin. The kinetics of both lipopeptides in the presence and absence of Ca2+ were quantitatively and qualitatively evaluated and further correlated with the cell cycle. The impairment of P. elgii AC13 sporogenesis had no effect on tridecaptin production, which remained undetected in the supernatant of the culture. On the other hand, the yield of pelgipeptin in a Ca2+-free medium increased. We showed for the first time that the removal of Ca2+ interrupted the sporogenesis in P. elgii and improved the yield of pelgipeptins. However, Ca2+ absence had no effect on tridecaptin yield, which is possibly degraded or associated with other cell debris components.
佩尔吉肽、十三肽和埃利希菌素是短小芽孢杆菌产生的抗菌肽之一。在复杂培养基中生长通常用于从培养物上清液中获得脂肽,但需要进一步纯化。本研究旨在使用化学成分确定的培养基来提高佩尔吉肽和十三肽的产量。在短小芽孢杆菌 AC13 中,评估了化学成分确定的培养基中抗菌脂肽产量的动力学。在培养物上清液和培养物沉淀中均检测到了佩尔吉肽,但十三肽主要与细胞碎片或内生孢子有关。我们研究了是否去除 Ca2+ 会损害短小芽孢杆菌的孢子形成,从而提高十三肽的产量。定量和定性地评估了存在和不存在 Ca2+ 时两种脂肽的动力学,并进一步与细胞周期相关联。去除短小芽孢杆菌 AC13 的孢子形成对十三肽的产生没有影响,其在培养物上清液中仍未被检测到。另一方面,在无 Ca2+的培养基中,佩尔吉肽的产量增加。我们首次表明,去除 Ca2+会中断短小芽孢杆菌的孢子形成,并提高佩尔吉肽的产量。然而,Ca2+的缺乏对十三肽的产量没有影响,它可能被降解或与其他细胞碎片成分相关联。