Table 1. Macromolecule-production information.

The NdeI site and BamHI site used for cloning are underlined in the forward and reverse primers, respectively.

Source organism	Pseudomonas sp. strain AAC
DNA source	gDNA
Forward primer	TTTTTTCATATGACGAAACAGACCAGCGCCCAGACCCAAC
Reverse primer	AAAAAAGGATCCTCAAGACAGCGCTACGGCGGCGGTTTG
Cloning vector	pETcc2
Expression vector	pETcc2
Expression host	E. coli Rosetta 2 (DE3)
Complete amino-acid sequence of the construct produced	MGSSHHHHHH SSGLVPRGSH MTKQTSAQTQ HWQALSREHH LAPFTDYKQL NEKGARIITK AEGVYLWDSE GNKILDGMAG LWCMNVGYGR KELAEVAYKQ MLELPYYNLF FQTAHPPALE LAKAIADIAP EGMNHVFFTG SGSESNDTVL RMVRHYWSIK GKPQKKVVIG RWNGYHGSTV AGVSLGGMKA LHSQGDLPIP GIVHIAQPYW YGEGGDMSAE EFGVWAAEQL EKKILEVGEE NVAAFIAEPI QGAGGVIVPP DTYWPKIREI LAKYEILFIA DEVICGFGRT GEWFGSQYYG NAPDLMPIAK GLTSGYIPMG GVIVRDEIVD TLNEGGEFYH GFTYSGHPVA AAVALENIRI LREEKIVETV KAETAPYLQK RWQELADHPL VGEARGVGMV GALELVKNKK TRERFENGVG MLCREHCFRN GLIMRAVGDT MIISPPLVIT KPEIDELITL ARKCLDQTAA VALS