The estimated size of Cthe_3148 indicates that it was isolated in an intact dimeric form. The solute binding Lazertinib solubility dmso protein (Cthe_1020, 49 kDa), the integral membrane protein (Cthe_1018, 32 kDa) and the ATP binding cassette protein (Cthe_1862, 42 kDa) were identified on a vertical line at ~190 kDa. In the genome of C. thermocellum, no ATP binding cassette proteins are found near Cthe_1020 and Cthe_1018, and Cthe_1862 is not adjacent to other BP or IM proteins. The identification of these proteins on a vertical line strongly suggests that they form a transporter complex. Cthe_1020 is an abundantly expressed protein under our culture condition, it was detected at ~100 kDa to over 880 kDa, and the high molecular

weight spots maybe result of protein precipitation during electrophoresis. Cthe_1555, Cthe_1556 and Cthe_1557 form an ABC transporter gene cluster Foretinib mw in the genome. The ATP binding cassette protein (Cthe_1557, 30 kDa) was detected at an estimated molecular mass of ~140 kDa. But the integral membrane protein Cthe_1556 (26 kDa) and solute binding protein Cthe_1555 (32 kDa) were not detected. The estimated size of this ABC transporter complex suggests it contains two subunits of Cthe_1557, two subunits Cthe_1556 and

one subunit of Cthe_1555 as an intact complex. Cthe_1555 was detected at ~100 kDa on a horizontal line with Cthe_1557, which could be due to dissociation of the transporter complex during electrophoresis. Cthe_1752, Cthe_1753 and Cthe_1754 form an ABC transporter gene cluster in the genome. The solute binding protein (Cthe_1754, 36 kDa) was selleck chemicals detected at ~170 kDa.

But the integral membrane protein Cthe_1753 (37 kDa) and ATP binding cassette protein Cthe_1752 (30 kDa) was not detected. The size of ABC second transporter complex estimated by BN-PAGE, suggests it contains two subunits Cthe_1752, two subunits Cthe_1753 and one subunit of Cthe_1754. In this study, we did not detect the proteins in other ABC transporter gene clusters studied in vitro by Nataf [58] except Cthe_1020. Other protein complexes In Gram-positive bacteria, S-layer proteins are known to non-covalently attach to the pyruvylated negatively-charged secondary cell wall polymers (SCWP) by the surface layer homology (SLH) domains [59–61]. We detected S-layer protein (Cthe_2348, 113 kDa) at ~140 kDa, probably in a monomeric form, and there maybe a fragment of SCWP tethered with S-layer protein. Prepilin (Cthe_1104, 19 kDa) was identified from 20 kDa to 180 kDa in the SDS gel, this may reflect that the prepilins were in a process of pilin assembly [62]. Hypothetical proteins Three hypothetical proteins (Cthe_0858, Cthe_2693 and Cthe_2709) were detected in our membrane sample. Although Cthe_0858 showed weak similarity to domains designated PRK 13665, pfam 12127 and COG4864. The functions of these domains or their corresponding proteins are not known.