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Infrared signatures of Bacillus bacteria: Clear IR distinctions between sporulated and vegetative cells with chemical assignments

机译:芽孢杆菌细菌的红外特征:带有化学成分的孢子和营养细胞之间清晰的IR区别

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This paper highlights the distinctions between the infrared (IR) absorption spectra of vegetative versus sporulated Bacillus bacteria. It is observed that there are unique signatures clearly associated with either the sporulated or the vegetative state, and that vegetative cells (and associated debris) can contribute to the spore spectra. A distinct feature at ~1739 cm~(-1) appears to be unique to vegetative cell spectra, and can also be used as an indicator of vegetative cells or cell debris in the spore spectra. The data indicate the band is caused by a phospholipid carbonyl bond and are consistent with, but do not prove it to be, either phosphatidyl ethanolamine (PE) or phosphatidyl glycerol (PG), the two major classes of phospholipids found in vegetative cells of Bacillus species. The endospore spectra show characteristic peaks at 1441, 1277, and 1015 cm~(-1) along with a distinct quartet of peaks at 766, 725, 701, and 659 cm~(-1). These are clearly associated with calcium dipicolinate trihydrate, CaDP·3H_2O. We emphasize that the spore peaks, especially the quartet, arise from the calcium dipicolinate trihydrate and not from dipicolinic acid or other dipicolinate hydrate salts. The CaDP·3H_2O vibrational peaks and the effects of hydration were studied using quantum chemistry in the PQS software package. The quartet is associated with many motions including contributions from the Ca~(2+) counterion and hydration waters including Ca-O-H bends, H_2O-Ca-O torsions and O-C-O bends. The 1441 and 1015 cm~(-1) modes are planar pyridine modes with the 1441 mode primarily a ring C-N stretch and the 1015 mode primarily a ring C-C stretch.
机译:本文着重介绍了营养性和散生性芽孢杆菌细菌的红外(IR)吸收光谱之间的区别。可以观察到,有明显的特征与孢子状或营养状态相关,并且营养细胞(和相关碎片)可以促进孢子光谱。 〜1739 cm〜(-1)处的明显特征似乎是营养细胞光谱所独有的,也可以用作孢子光谱中营养细胞或细胞碎片的指示剂。数据表明该条带是由磷脂羰基键引起的,与芽孢杆菌营养细胞中发现的两大类磷脂磷脂酰乙醇胺(PE)或磷脂酰甘油(PG)一致,但没有证明种类。内生孢子谱显示在1441、1277和1015 cm-1(-1)处有特征峰,在766、725、701和659 cm-1(-1)处有明显的四重峰。这些显然与二吡啶甲酸钙三水合物CaDP·3H_2O有关。我们强调孢子峰,特别是四重峰,是由二吡啶甲酸钙三水合物产生的,而不是由二吡啶甲酸或其他二吡啶甲酸水合物盐引起的。在PQS软件包中使用量子化学研究了CaDP·3H_2O的振动峰和水合作用的影响。四重奏与许多运动相关,包括来自Ca〜(2+)抗衡离子和水化水的贡献,包括Ca-O-H弯曲,H_2O-Ca-O扭转和O-C-O弯曲。 1441和1015 cm〜(-1)模式是平面吡啶模式,其中1441模式主要是环C-N延伸,而1015模式主要是环C-C延伸。

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